kprx-20260930

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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, D.C. 20549

FORM 10-Q


x			QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the quarterly period ended September 30, 2026


o			TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the transition period from ___________ to ___________

Commission File No. 001-36672

KIORA PHARMACEUTICALS, INC.

(Exact Name of Registrant as Specified in Its Charter)


Delaware			98-0443284
(State or other jurisdiction of Incorporation or organization)			(I.R.S. Employer Identification No.)

169 Saxony Rd.

Suite 212

Encinitas, CA 92024

(Address of Principal Executive Offices, including zip code)

(858) 224-9600

(Registrant’s telephone number, including area code)

Securities registered pursuant to Section 12(b) of the Act:


Title of each class	Trading symbol(s)	Name of each exchange on which registered
Common Stock, $0.01 par value	KPRX	The Nasdaq Capital Market

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. x Yes o No

Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T during the preceding 12 months (or for such shorter period that the registrant was required to submit). x Yes o No

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company, or an emerging growth company. See the definitions of “large accelerated filer”, “accelerated filer”, “smaller reporting company” and “emerging growth company” in Rule 12b-2 of the Exchange Act.

Large Accelerated filer

Accelerated filer

Non-accelerated filer

Smaller reporting company

Emerging growth company

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. o

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act.)

o Yes x No

On November 10, 2026, there were 4,424,387 shares of the registrant’s common stock outstanding.

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KIORA PHARMACEUTICALS, INC.

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QUARTERLY REPORT ON FORM 10-Q

For the Periods Ended September 30, 2026

INDEX


		Page
PART I - FINANCIAL INFORMATION

Item 1.	Financial Statements	4

	Condensed Consolidated Balance Sheets as of September 30, 2026 (unaudited) and December 31, 2025	4

	Condensed Consolidated Statements of Operations and Comprehensive Loss (unaudited) for the Three and Nine Months Ended September 30, 2026 and 2025	5

	Condensed Consolidated Statements of Stockholders’ Equity (unaudited) for the Three and Nine Months Ended September 30, 2026 and 2025	6

	Condensed Consolidated Statements of Cash Flows (unaudited) for the Nine Months Ended September 30, 2026 and 2025	9

	Notes to Condensed Consolidated Financial Statements (unaudited)	10

Item 2.	Management’s Discussion and Analysis of Financial Condition and Results of Operations	33

Item 3.	Quantitative and Qualitative Disclosures about Market Risk	39

Item 4.	Controls and Procedures	40

PART II - OTHER INFORMATION

Item 1.	Legal Proceedings	41

Item 1A.	Risk Factors	41

Item 2.	Unregistered Sales of Equity Securities and Use of Proceeds	41

Item 3.	Defaults Upon Senior Securities	42

Item 4.	Mine Safety Disclosures	42

Item 5.	Other Information	42

Item 6.	Exhibits	42

SIGNATURES		43

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FORWARD-LOOKING STATEMENTS

This Quarterly Report on Form 10-Q contains statements that are not statements of historical fact and are forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, or the Securities Act, and Section 21E of the Securities Exchange Act of 1934, as amended, or the Exchange Act. The forward-looking statements are principally, but not exclusively, contained in “Item 2: Management’s Discussion and Analysis of Financial Condition and Results of Operations.” These statements involve known and unknown risks, uncertainties and other factors that may cause our actual results, performance, or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. Forward-looking statements include, but are not limited to, statements about management’s confidence or expectations, and our plans, objectives, expectations, and intentions that are not historical facts. In some cases, you can identify forward-looking statements by terms such as “may,” “will,” “should,” “could,” “would,” “expect,” “plan,” “anticipate,” “believe,” “goal,” "foreseeable," “see,” “estimate,” “project,” “intends,” “think,” “potential,” “objective,” “optimistic,” “strategy,” and similar expressions intended to identify forward-looking statements. These statements reflect our current views with respect to future events and are based on assumptions and subject to risks and uncertainties. Given these uncertainties, you should not place undue reliance on these forward-looking statements. Forward-looking statements include, but are not limited to, statements about:

•the timing and success of preclinical studies and clinical trials conducted by us and our development partners;

•the ability to obtain and maintain regulatory approval of our product candidates, and the labeling for any approved products;

•the scope, progress, expansion, and costs of developing and commercializing our product candidates;

•the size and growth of the potential markets for our product candidates and the ability to serve those markets;

•our expectations regarding our expenses and revenue, the sufficiency of our cash resources and needs for additional financing;

•the rate and degree of market acceptance of any approved products;

•our expectations regarding competition;

•our anticipated growth strategies;

•our ability to attract or retain key personnel;

•our ability to establish and maintain development partnerships;

•our expectations regarding federal, state and foreign regulatory requirements;

•regulatory developments in the U.S. and foreign countries;

•our ability to obtain and maintain intellectual property protection for our product candidates;

•the anticipated trends and challenges in our business and the market in which we operate;

•our ability to assess the probability of achievement of milestones and other advances in our product candidates;

•the timing and our ability to satisfy our obligations under the KIO-401 License Agreement with Senju, including milestone and royalty payments; and

•our ability to partner or out-license any of our product candidates.

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We discuss many of these risks in detail under the heading “Item 1A. Risk Factors” beginning on page 21 of our Annual Report on Form 10-K for the fiscal year ended December 31, 2025, as filed with the Securities and Exchange Commission, or the SEC, on March 25, 2026, or the Annual Report. You should carefully review all of these factors, as well as other risks described in our public filings, and you should be aware that there may be other factors, including factors of which we are not currently aware, that could cause these differences.

Also, these forward-looking statements represent our estimates and assumptions only as of the date of this report. We may not update these forward-looking statements, even though our situation may change in the future, unless we have obligations under the federal securities laws to update and disclose material developments related to previously disclosed information.

Kiora Pharmaceuticals, Inc. is referred to herein as “we,” “our,” “us,” and “the Company.”

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PART I - FINANCIAL INFORMATION

Item 1. Financial Statements

KIORA PHARMACEUTICALS, INC.

CONDENSED CONSOLIDATED BALANCE SHEETS


	September 30, 2026 (unaudited)		December 31, 2025
ASSETS
Current Assets:
Cash and Cash Equivalents	$	5,570,640	$	8,696,570
Short-Term Investments	10,716,331		8,392,513
Prepaid Expenses and Other Current Assets	1,008,822		1,141,804
Collaboration Receivables	636,756		1,522,770
Tax and Other Receivables	1,579,103		1,793,459
Prepaid Collaboration Expenses	402,437		201,332
Total Current Assets	19,914,089		21,748,448
Non-Current Assets:
Property and Equipment, Net	88,192		91,672
Restricted Cash	4,765		4,566
Intangible Assets and In-Process R&D, Net	2,063,100		2,063,100
Operating Lease Right-of-Use Assets	219,565		285,827
Other Assets	84,351		59,687
Total Assets	$	22,374,062	$	24,253,300
LIABILITIES AND STOCKHOLDERS’ EQUITY
Current Liabilities:
Accounts Payable	$	209,074	$	1,060,306
Accrued Expenses	2,147,562		2,406,731

Operating Lease Liabilities	162,095		164,461
Total Current Liabilities	2,518,731		3,631,498
Non-Current Liabilities:
Contingent Consideration	3,082,326		2,939,316
Deferred Tax Liability	102,152		102,152
Deferred Collaboration Revenue	1,250,000		1,250,000
Non-Current Operating Lease Liabilities	124,694		203,798
Total Non-Current Liabilities	4,559,172		4,495,266
Total Liabilities	7,077,903		8,126,764
Commitments and Contingencies (Note 9)
Stockholders’ Equity:
Preferred Stock, $0.01 Par Value: 10,000,000 shares authorized; 3,750 designated Series A, 0 shares issued and outstanding; 10,000 designated Series B, 0 shares issued and outstanding; 10,000 shares designated Series C, 0 shares issued and outstanding; 20,000 shares designated Series D, 7 shares issued and outstanding; 1,280 shares designated Series E, 0 shares issued and outstanding; 3,908 shares designated Series F, 420 issued and outstanding at September 30, 2026 and December 31, 2025, respectively	4		4
Common Stock, $0.01 Par Value: 150,000,000 shares authorized; 4,424,387 and 3,761,739 shares issued and outstanding at September 30, 2026 and December 31, 2025, respectively	281,915		275,289
Additional Paid-In Capital	175,723,637		170,314,656
Accumulated Deficit	(160,463,791)		(154,217,276)
Accumulated Other Comprehensive Loss	(245,606)		(246,137)
Total Stockholders’ Equity	15,296,159		16,126,536
Total Liabilities and Stockholders’ Equity	$	22,374,062	$	24,253,300

See Accompanying Notes to Condensed Consolidated Financial Statements.

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KIORA PHARMACEUTICALS, INC.

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND

COMPREHENSIVE LOSS

(unaudited)


	Three Months Ended September 30,				Nine Months Ended September 30,
	2026		2025		2026		2025
Revenue:
Collaboration Revenue	$	1,000,000	$	—	$	1,000,000	$	—

Total Revenue	1,000,000		—		1,000,000		—
Operating Expenses:
General and Administrative	$	1,580,111	$	1,443,827	$	4,575,882	$	4,287,075
Research and Development	1,949,864		2,729,891		6,150,705		7,852,267
Collaboration Credits	(885,559)		(1,658,248)		(3,455,046)		(5,310,288)


Change in Fair Value of Contingent Consideration	46,169		(1,721,033)		143,010		(1,308,067)
Total Operating Expenses	2,690,585		794,437		7,414,551		5,520,987
Operating Loss	(1,690,585)		(794,437)		(6,414,551)		(5,520,987)
Other Income (Expense), Net:


Interest Income, Net	146,306		201,822		431,876		703,692
Other Expense, Net	(40,242)		(23,708)		(98,040)		(133,517)
Total Other Income, Net	106,064		178,114		333,836		570,175
Loss Before Income Tax (Expense) Benefit	(1,584,521)		(616,323)		(6,080,715)		(4,950,812)
Income Tax (Expense) Benefit	(165,000)		643,129		(165,800)		632,179
Net (Loss) Income	$	(1,749,521)	$	26,806	$	(6,246,515)	$	(4,318,633)

Net (Loss) Income Attributable to Common Shareholders	$	(1,749,521)	$	26,806	$	(6,246,515)	$	(4,318,633)
Net (Loss) Income per Common Share - Basic	$	(0.28)	$	0.01	$	(1.12)	$	(1.04)
Weighted Average Shares Outstanding - Basic	6,295,123		4,289,853		5,556,915		4,165,568
Net (Loss) Income per Common Share - Diluted	$	(0.28)	$	0.01	$	(1.12)	$	(1.04)
Weighted Average Shares Outstanding - Diluted	6,295,123		4,361,740		5,556,915		4,165,568

Other Comprehensive Loss:
Net (Loss) Income	$	(1,749,521)	$	26,806	$	(6,246,515)	$	(4,318,633)
Unrealized (Loss) Gain on Marketable Securities	(11,184)		11,214		(30,520)		(16,001)
Foreign Currency Translation Adjustments	21,375		(9,153)		31,050		54,451
Comprehensive (Loss) Income	$	(1,739,330)	$	28,867	$	(6,245,985)	$	(4,280,183)

See Accompanying Notes to Condensed Consolidated Financial Statements.

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KIORA PHARMACEUTICALS, INC.

CONDENSED CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY

Three Months Ended September 30, 2026 and 2025

(unaudited)


	Preferred Stock			Common Stock			Additional Paid-In Capital		Accumulated Deficit		Accumulated Other Comprehensive Loss		Total Stockholders’ Equity
	Shares	Amount		Shares	Amount
Balance at June 30, 2026	427	$	4	4,427,167	$	281,943	$	175,544,810	$	(158,714,270)	$	(255,797)	$	16,856,689

Stock-based compensation	—	—		—	—		186,196		—		—		186,196



Shares withheld for employee taxes on vested restricted stock	—	—		(2,780)	(28)		(7,369)		—		—		(7,397)





Unrealized Loss on Investments	—	—		—	—		—		—		(11,184)		(11,184)

Foreign currency translation adjustment	—	—		—	—		—		—		21,375		21,375

Net Loss	—	—		—	—		—		(1,749,521)		—		(1,749,521)

Balance at September 30, 2026	427	$	4	4,424,387	$	281,915	$	175,723,637	$	(160,463,791)	$	(245,606)	$	15,296,159


	Preferred Stock			Common Stock			Additional Paid-In Capital		Accumulated Deficit		Accumulated Other Comprehensive Loss		Total Stockholders’ Equity
	Shares	Amount		Shares	Amount
Balance at June 30, 2025	427	$	4	3,433,491	$	272,006	$	169,828,797	$	(147,727,560)	$	(245,769)	$	22,127,478

Stock-based compensation	—	—		—	—		254,397		—		—		254,397





Unrealized Gain on Investments	—	—		—	—		—		—		11,214		11,214

Foreign currency translation adjustment	—	—		—	—		—		—		(9,153)		(9,153)

Net Income	—	—		—	—		—		26,806		—		26,806

Balance at September 30, 2025	427	$	4	3,433,491	$	272,006	$	170,083,194	$	(147,700,754)	$	(243,708)	$	22,410,742

See Accompanying Notes to Condensed Consolidated Financial Statements.

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KIORA PHARMACEUTICALS, INC.

CONDENSED CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY

Nine Months Ended September 30, 2026 and 2025

(unaudited)


	Preferred Stock			Common Stock			Additional Paid-In Capital		Accumulated Deficit		Accumulated Other Comprehensive Loss		Total Stockholders’ Equity
	Shares	Amount		Shares	Amount
Balance at December 31, 2025	427	$	4	3,761,739	$	275,289	$	170,314,656	$	(154,217,276)	$	(246,136)	$	16,126,536

Stock-based compensation	—	—		—	—		505,016		—		—		505,016

Issuance of Common Stock from Restricted Stock Awards	—	—		43,341	433		(433)		—		—		—

Withhold to Cover RSAs	—	—		(8,053)	(81)		(17,645)		—		—		(17,726)





Issuance of Common Stock from Warrant Exercises	—	—		188,889	1,889		(1,719)		—		—		170

Issuance of Common Stock and Warrants from Private Placement, Net of Offering Costs of $72 thousand	—	—		438,471	4,385		4,923,762		—		—		4,928,147

Unrealized Loss on Investments	—	—		—	—		—		—		(30,520)		(30,520)

Foreign currency translation adjustment	—	—		—	—		—		—		31,050		31,050

Net Loss	—	—		—	—		—		(6,246,515)		—		(6,246,515)

Balance at September 30, 2026	427	$	4	4,424,387	$	281,915	$	175,723,637	$	(160,463,791)	$	(245,606)	$	15,296,159

See Accompanying Notes to Condensed Consolidated Financial Statements.

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KIORA PHARMACEUTICALS, INC.

CONDENSED CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY

Nine Months Ended September 30, 2026 and 2025

(unaudited)


	Preferred Stock			Common Stock			Additional Paid-In Capital		Accumulated Deficit		Accumulated Other Comprehensive Loss		Total Stockholders’ Equity
	Shares	Amount		Shares	Amount
Balance at December 31, 2024	427	$	4	3,000,788	$	267,679	$	169,156,374	$	(143,382,122)	$	(282,159)	$	25,759,776

Stock-based compensation	—	—		—	—		665,788		—		—		665,788



Issuance of Common Stock from Warrant Exercises	—	—		389,634	3,896		261,464		—		—		265,360



Issuance of Common Stock from Restricted Stock Awards	—	—		43,069	431		(431)		—		—		—

Unrealized Loss on Investments	—	—		—	—		—		—		(16,001)		(16,001)

Foreign currency translation adjustment	—	—		—	—		—		—		54,451		54,451

Net Loss	—	—		—	—		—		(4,318,633)		—		(4,318,633)

Balance at September 30, 2025	427	$	4	3,433,491	$	272,006	$	170,083,194	$	(147,700,754)	$	(243,708)	$	22,410,742

See Accompanying Notes to Condensed Consolidated Financial Statements.

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KIORA PHARMACEUTICALS, INC.

CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS (unaudited)


	Nine Months Ended September 30,
	2026		2025
Operating Activities:
Net Loss	$	(6,246,515)	$	(4,318,633)
Adjustments to Reconcile Net Loss to Net Cash Used in Operating Activities:
Depreciation and Amortization	33,445		14,293

Reduction of Operating Lease Right-of-Use Assets	114,149		75,047
Stock-Based Compensation	505,016		665,788

Change in Fair Value of Contingent Consideration	143,010		(1,308,067)


Accretion of Discount on Marketable Securities	(11,530)		(109,113)
Change in Accrued Interest on Marketable Securities	74,855		118,188
Net Realized Gain on Marketable Securities	(5)		(1,892)
Change in Unrealized Gain on Cash Equivalents	(1)		(119)
Changes in Operating Assets and Liabilities:
Prepaid Expenses and Other Current Assets	(19,257)		747,470
Collaboration Receivables	886,014		(612,029)

Tax and Other Receivables	219,829		(1,154,482)
Prepaid Collaboration Expenses	(194,416)		(945,267)
Other Assets	(23,383)		(32,617)
Accounts Payable	(689,633)		469,015
Accrued Expenses	(272,667)		(2,571,553)
Deferred Collaboration Revenue	—		1,250,000
Operating Lease Liabilities	(129,695)		(66,750)
Net Cash Used in Operating Activities	(5,610,785)		(7,780,721)
Investing Activities:
Purchases of Property and Equipment	(28,829)		(32,626)

Purchases of Marketable Securities	(12,092,656)		(8,175,851)
Sales of Marketable Securities	—		305,000
Maturities of Marketable Securities	9,675,000		16,981,000
Net Cash (Used In) Provided by Investing Activities	(2,446,485)		9,077,523
Financing Activities:


Gross Proceeds from Private Placement	4,999,848		—
Issuance Costs for Private Placement	(71,701)		—

Taxes Paid Related to Net Share Settlement of Equity Awards	(17,725)		—
Exercise of Warrants	170		265,359
Proceeds from Line of Credit	—		2,750,000
Repayments of Line of Credit	—		(2,750,000)
Net Cash Provided by Financing Activities	4,910,592		265,359
Effect of Exchange Rate Changes on Cash, Cash Equivalents and Restricted Cash	20,947		154,879
Net (Decrease) Increase in Cash, Cash Equivalents and Restricted Cash	(3,125,731)		1,717,040
Cash, Cash Equivalents and Restricted Cash, Beginning of Period	8,701,136		3,796,379
Cash, Cash Equivalents and Restricted Cash, End of Period	$	5,575,405	$	5,513,419

Supplemental Disclosures of Noncash Operating and Financing Activities
Creation of Right-of-Use Assets and Related Lease Liabilities	$	50,742	$	335,280

Grant of Restricted Stock Awards	$	433	$	431
Tenant Improvements Paid Directly by Lessor	$	—	$	72,810

See Accompanying Notes to Condensed Consolidated Financial Statements.

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KIORA PHARMACEUTICALS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (unaudited)

September 30, 2026

1. Business, Presentation and Recent Accounting Pronouncements

Overview

Kiora Pharmaceuticals, Inc. (“Kiora” or the “Company”) was formed as a Delaware corporation on December 28, 2004. Kiora is a clinical-stage specialty pharmaceutical company developing and commercializing therapies for the treatment of retinal diseases.

Since its inception, Kiora has devoted substantially all its efforts to business planning, research and development, and raising capital.

Unaudited Interim Financial Information

The accompanying unaudited condensed consolidated financial statements of the Company have been prepared in accordance with accounting principles generally accepted in the United States (“U.S. GAAP”) for interim financial information and with the instructions to Form 10-Q and Rule 8-03 of Regulation S-X. Pursuant to these rules and regulations, they do not include all information and notes required by U.S. GAAP for complete financial statements. In the opinion of management, all adjustments (consisting of normal recurring adjustments) considered necessary for a fair presentation of the Company’s financial condition and results of operations have been included. Operating results for the periods presented are not necessarily indicative of the results that may be expected for the full year. We believe that the disclosures provided herein are adequate to make the information presented not misleading when these unaudited interim condensed consolidated financial statements are read in conjunction with the audited consolidated financial statements and notes previously included in the Company’s 2025 Annual Report on Form 10-K dated March 25, 2026. The accompanying balance sheet as of December 31, 2025 was derived from audited consolidated financial statements of the Company but does not include all the disclosures required by U.S. GAAP.

Adoption of Accounting Standards

In December 2023, the FASB issued ASU 2023-09, Income Taxes (Topic 740) - Improvements to Income Tax Disclosures. The new standard requires a company to expand its existing income tax disclosures, specifically related to the rate reconciliation and income taxes paid. The standard is effective for public companies beginning in fiscal year 2025 for the annual reporting period ending December 31, 2025, with early adoption permitted. The Company adopted ASU 2023-09 on January 1, 2025. The adoption of ASU 2023-09 did not have a material effect on the condensed consolidated financial statements and related disclosures.

Accounting Standards Pending Adoption

In November 2024, the FASB issued ASU 2024-03, Disaggregation of Income Statement Expenses (“ASU 2024-03”). The guidance in ASU 2024-03 requires new financial statement disclosures in tabular format, disaggregating information about prescribed categories underlying any relevant income statement expense captions. The standard is effective for fiscal years beginning after December 15, 2026 and interim periods within fiscal years beginning after December 15, 2027, with early adoption permitted. Upon adoption, ASU 2024-03 may be applied prospectively or retrospectively. The Company is currently evaluating the impact that the adoption of ASU 2024-03 may have on its disclosures in its condensed consolidated financial statements.

In December 2025, the FASB issued ASU No. 2025-11, Interim Reporting. This ASU was issued to enhance consistency in interim reporting for all entities by providing clarity about the current interim reporting requirements and creating a comprehensive list of interim disclosures required under US GAAP. The standard is effective for interim reporting periods within annual reporting periods beginning after December 15, 2027. Early adoption is permitted and amendments can be applied either prospectively or retrospectively. The Company is currently evaluating the impact of the adoption of this standard on its interim disclosures.

Liquidity and Capital Resources

The accompanying condensed consolidated financial statements have been prepared assuming that the Company will continue as a going concern, which contemplates the realization of assets and satisfaction of liabilities in the normal course of business. At September 30, 2026, the Company had unrestricted Cash and

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KIORA PHARMACEUTICALS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (unaudited)

September 30, 2026

Cash Equivalents of $5.6 million and Short-term Investments of $10.7 million, and an Accumulated Deficit of $160.5 million. Subsequent to the reporting period, in October 2026, the Company entered into a license agreement with Senju Pharmaceutical Co., Ltd. (“Senju”), (the "KIO-401 License Agreement"), under which the Company will pay Senju a $3.5 million upfront payment and a $12.5 million technology transfer milestone (see Note 13). With the exception of the year ended December 31, 2024, Kiora has incurred annual losses and negative cash flows since inception, and future losses are anticipated. Based on the cash and short-term investments on hand at September 30, 2026, the Company anticipates having sufficient cash to fund its planned operations into late 2027, excluding the technology transfer milestone, which may become payable prior to such date. The acceleration or reduction of cash outflows by management can significantly impact the timing for the need to raise capital to complete development of its products. To continue development, Kiora will need to raise additional capital through equity financing, license agreements, and/or grants. Although historically the Company has been successful at raising capital, most recently raising net proceeds of approximately $4.9 million in a private offering that closed on April 6, 2026, as well as an equity line of credit that provides an additional $10 million (subject to certain limitations), additional capital may not be available on terms favorable to Kiora, if at all. The Company does not know if any future offerings will succeed. Accordingly, no assurances can be given that Company management will succeed in these endeavors. The factors described above have caused management to determine there is substantial doubt about the Company’s ability to continue as a going concern. The accompanying condensed consolidated financial statements do not include any adjustments to reflect the possible future effects on the recoverability and classification of assets or the amounts and classification of liabilities or any other adjustments that might be necessary should the Company be unable to continue as a going concern

Significant Accounting Policies

Cash and Cash Equivalents

The Company considers all highly liquid investments with original maturities of three months or less when purchased to be cash equivalents. Cash and cash equivalents include cash in readily available checking accounts, savings accounts, money market funds, and marketable securities with maturities of 3 months or less when acquired. The carrying amounts reported in the unaudited condensed balance sheets for cash and cash equivalents are valued at cost, which approximates fair value.

Short-Term Investments

Short-term investments primarily consist of treasuries, corporate debt securities, and government and agency securities. The Company has classified these investments as available-for-sale securities, as the sale of such investments may be required prior to maturity to implement management strategies, and therefore has classified all investments with maturity dates beyond three months at the date of purchase as current assets in the accompanying unaudited condensed consolidated balance sheets. Any premium or discount arising at purchase is amortized and/or accreted to interest income as an adjustment to yield using the straight-line method over the life of the instrument. Investments are reported at their estimated fair value. Unrealized gains and losses are included in accumulated other comprehensive loss as a component of stockholders' equity until realized.

Allowance for Credit Losses

For available-for-sale securities in an unrealized loss position, the Company first assesses whether it intends to sell, or if it is more likely than not that it will be required to sell, the security before recovery of its amortized cost basis. If either of the criteria regarding intent or requirement to sell is met, the security’s amortized cost basis is written down to fair value through earnings. For available-for-sale securities that do not meet the aforementioned criteria, the Company evaluates whether the decline in fair value has resulted from credit losses or other factors. In making this assessment, the Company considers the severity of the impairment, any changes in interest rates, market conditions, changes to the underlying credit ratings and forecasted recovery, among other factors. The credit-related portion of unrealized losses, and any subsequent improvements, are recorded in interest income through an allowance account. Any impairment that has not been recorded through an allowance for credit losses is included in other comprehensive loss on the condensed consolidated balance sheets.

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KIORA PHARMACEUTICALS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (unaudited)

September 30, 2026

The Company excludes the applicable accrued interest from both the fair value and amortized cost basis of available-for-sale securities for purposes of identifying and measuring an impairment. Accrued interest receivable on investment securities is recorded within prepaid expenses and other current assets on the condensed consolidated balance sheets. The Company’s accounting policy is to not measure an allowance for credit loss for accrued interest receivable and to write-off any uncollectible accrued interest receivable as a reversal of interest income in a timely manner, which is considered to be in the period in which it is determined the accrued interest will not be collected.

Impairment of Long-Lived Assets

The Company evaluates potential impairment of long-lived assets and long-lived assets to be disposed of and considers whether long-lived assets held for use have been impaired whenever events or changes in circumstances indicate that the related carrying amount may not be recoverable, or that the period of their recovery may have changed. Management makes significant estimates and assumptions regarding future sales, cost trends, productivity and market maturity in order to test for impairment. Management reports those long-lived assets to be disposed of and assets held for sale at the lower of carrying amount or fair value less cost to sell. Based on current facts, estimates and assumptions, management believes that no assets are impaired at September 30, 2026. There is no assurance that management’s estimates and assumptions will not change in future periods.

Revenue Recognition

In accordance with FASB’s ASC 606, Revenue from Contracts with Customers, or ASC 606, the Company recognizes revenue when its customer obtains control of promised goods or services, in an amount that reflects the consideration which the entity expects to receive in exchange for those goods or services. To determine revenue recognition for arrangements that the Company determines are within the scope of ASC 606, it performs the following five steps: (i) identify the contract(s) with a customer; (ii) identify the performance obligations in the contract; (iii) determine the transaction price; (iv) allocate the transaction price to the performance obligations in the contract; and (v) recognize revenue when (or as) the entity satisfies a performance obligation.

The Company applies the five-step model to contracts when it determines that it is probable it will collect the consideration it is entitled to in exchange for the goods or services it transfers to the customer. At contract inception, once the contract is determined to be within the scope of ASC 606, the Company assesses the goods or services promised within each contract and determines those that are performance obligations, and assesses whether each promised good or service is distinct. The Company then recognizes as revenue the amount of the transaction price that is allocated to the respective performance obligation when (or as) the performance obligation is satisfied.

In a contract with multiple performance obligations, we must develop estimates and assumptions that require judgment to determine the underlying stand-alone selling price for each performance obligation which determines how the transaction price is allocated among the performance obligation. The estimation of the stand-alone selling price(s) may include estimates regarding forecasted revenues or costs, development timelines, discount rates, and probabilities of technical and regulatory success. We evaluate each performance obligation to determine if it can be satisfied at a point in time or over time. Any change made to estimated progress towards completion of a performance obligation and, therefore, revenue recognized will be recorded as a change in estimate. In addition, variable consideration must be evaluated to determine if it is constrained and, therefore, excluded from the transaction price.

During the three and nine months ended September 30, 2026, the Company recognized $1.0 million of collaboration revenue related to the upfront payment under its license agreement with Chong Kun Dang Pharmaceutical Corporation (see Note 8). No revenue was recognized during the three and nine months ended September 30, 2025. Amounts received prior to satisfying the revenue recognition criteria are recognized as deferred revenue in the Company’s balance sheet. Amounts expected to be recognized as revenue within the twelve months following the balance sheet date are classified as the current portion of deferred revenue. Amounts not expected to be recognized as revenue within the twelve months following the balance sheet date are classified as deferred revenue, net of current portion. As of September 30, 2026 and December 31, 2025, the Company had a deferred revenue balance of $1.25 million.

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KIORA PHARMACEUTICALS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (unaudited)

September 30, 2026

Collaboration Revenue

If a license to our intellectual property is determined to be distinct from the other performance obligations identified in a contract, the Company recognizes revenues from the transaction price allocated to the license when the license is transferred to the licensee and the licensee is able to use and benefit from the license. For licenses that are bundled with other promises, the Company utilizes judgment to assess the nature of the combined performance obligation to determine whether the combined performance obligation is satisfied over time or at a point in time and, if over time, the appropriate method of measuring progress for purposes of recognizing revenue from the allocated transaction price. The Company evaluates the measure of progress at each reporting period and, if necessary, adjusts the measure of performance and related revenue or expense recognition as a change in estimate.

At the inception of each arrangement that includes milestone payments, the Company evaluates whether the milestones are considered probable of being reached. If it is probable that a significant revenue reversal would not occur, the associated milestone value is included in the transaction price. Milestone payments that are not within the Company's or a collaboration partner’s control, such as regulatory approvals, are generally not considered probable of being achieved until those approvals are received. At the end of each reporting period, the Company re-evaluates the probability of achievement of milestones that are within the Company's or a collaboration partner’s control, such as operational development milestones and any related constraint, and, if necessary, adjust our estimate of the overall transaction price. Any such adjustments are recorded on a cumulative catch-up basis, which will affect collaboration revenues and earnings in the period of adjustment. Revisions to the Company's estimate of the transaction price may also result in negative collaboration revenues and earnings in the period of adjustment.

For arrangements that include sales-based royalties, including commercial milestone payments based on the level of sales, and a license is deemed to be the predominant item to which the royalties relate, the Company will recognize revenue at the later of (i) when the related sales occur, or (ii) when the performance obligation to which some or all of the royalty has been allocated has been satisfied, or partially satisfied.

Revenue from licenses is recognized gross of any foreign taxes withheld by the licensee. Foreign withholding taxes are income taxes of the Company and are recognized in the income tax provision.

Sublicense fees payable to the Company’s licensors that are incremental costs of obtaining a contract with a customer are recognized as an asset and expensed on a basis consistent with the transfer of the license to which they relate. When the related license is transferred at a point in time, the sublicense fee is expensed in that period; sublicense fees on milestone payments are expensed in the period the related milestone revenue is recognized.

Collaboration Agreements

The Company has entered into license agreements with Théa Open Innovation (“TOI”) and Chong Kun Dang Pharmaceutical Corporation (“CKD”), an option agreement with Senju and subsequent to the reporting period, in October 2026, the Company entered into a license agreement with Senju, that fall under the scope of ASC 808, Collaborative Arrangements. For units of account within these arrangements for which the collaboration partner is a customer, such as licenses of the Company’s intellectual property, the Company applies ASC 606 and presents the related amounts as collaboration revenue. For collaborative activities in which the partner is not a customer, such as participation in joint steering committees and the related exchange of development information, the Company applies ASC 808. Reimbursements from a collaboration partner are recorded as a reduction to research and development expense in the condensed consolidated statements of operations and comprehensive loss. Similarly, amounts that are owed to a collaboration partner are recognized as research and development expense in the condensed consolidated statements of operations and comprehensive loss.

In-Process Research and Development

The Company expenses in-process R&D projects acquired in asset acquisitions that have not reached technological feasibility and which have no alternative future use. For in-process R&D projects acquired in business combinations, the Company capitalizes the in-process R&D project as an indefinite-lived intangible asset and evaluates this asset at least annually for impairment until the R&D process has been completed.

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KIORA PHARMACEUTICALS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (unaudited)

September 30, 2026

Once the R&D process is complete, the Company amortizes the R&D asset over its remaining useful life. The Company performed an annual evaluation of its indefinite-lived intangible assets for impairment as of December 31, 2025 with a quantitative analysis using the Income Approach. As previously reported, the analysis included a market capitalization reconciliation and completely independent of asset performance, indicated an impairment of $4.6 million of the KIO-104 program. Management believes this was directly related to the decline in the Company's stock price from August 31, 2025 to December 31, 2025 and corresponding market capitalization during this period. There were no adverse changes in clinical progress, development timelines, probability of technical success, or projected cash flows for the KIO-104 program. At September 30, 2026 and December 31, 2025, there was $2.1 million of in-process R&D as part of intangible assets and in-process R&D, net, on the condensed consolidated balance sheets. In October 2026, subsequent to entering into the KIO-401 License Agreement the Company decided to discontinue further research and development of KIO-104. The Company will evaluate the related $1.0 million in-process R&D asset for impairment in the fourth quarter of 2026 (see Note 13).

Accrued Clinical Expenses

As part of the Company’s process of preparing the condensed consolidated financial statements, the Company is required to estimate its accrued expenses. This process includes reviewing open contracts and purchase orders, communicating with its applicable personnel to identify services that have been performed on its behalf and estimating the level of service performed and the associated costs incurred for the service when the Company has not yet been invoiced or otherwise notified of actual costs. The majority of the Company’s service providers invoice monthly in arrears for services performed. The Company makes estimates of its accrued expenses as of each balance sheet date in the financial statements based on facts and circumstances known at the time. The Company periodically confirms the accuracy of these estimates with the service providers and makes adjustments if necessary.

Business Segment and Geographical Information

The Company identifies operating segments as components of the enterprise for which separate discrete financial information is available for evaluation by the chief operating decision maker, or decision-making group, in making decisions on how to allocate resources and assess performance. The Company views its operations and manages its business as fully integrated and operating in one business segment and three geographic areas. The Company's singular focus is developing innovative retinal pharmaceutical products.

Refunds for Research and Development

The Company through its subsidiaries, Kiora Pharmaceuticals GmbH and Kiora Pharmaceuticals Pty Ltd., is eligible to receive certain refundable tax incentives associated with its research and development expenses in Austria and Australia, respectively. These refunds are realized in the form of a cash payment when received, following the eligible incurred research and development expenses. Following the approval of a research finding by the tax authority, the Company records the refundable payment as a tax receivable and a reduction in expense in the period in which the research and development expenses are incurred. In situations where a new research application has not yet been approved by the tax authority, the Company records the tax receivable and reduction of expense in the period following approval. As of September 30, 2026 and December 31, 2025, the Company had research and development tax credit receivables of $0.5 million and $0.7 million, respectively.

Stock-Based Compensation

Stock-based compensation represents the cost related to stock-based awards granted to employees and others. The Company measures stock-based compensation cost to employees and non-employees at grant date, based on the estimated fair value of the award. Compensation cost for employee awards is recognized as expense on a straight-line basis over the employee requisite service period. The Company estimates the fair value of stock options using the Black-Scholes valuation model. The Company recorded compensation expense for non-employee awards with graded vesting using the accelerated expense attribution method. The Company’s policy is to record forfeitures as they occur.

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KIORA PHARMACEUTICALS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (unaudited)

September 30, 2026

The Company's equity incentive plan permits the satisfaction of employee tax withholding obligations on vested restricted stock awards through either (i) a sell-to-cover arrangement, in which the Company facilitates the sale of a portion of the vested shares in the open market and remits the proceeds to taxing authorities on the employee's behalf, or (ii) net share settlement, in which the Company withholds a portion of the vesting shares with an aggregate fair market value equal to the employee's statutory tax withholding obligation and remits cash to the applicable taxing authorities. The Company's preferred method is sell-to-cover. During 2026, the Company permitted net share settlement on a limited basis, although the Company does not anticipate net share settlement to be its standard practice. For shares withheld under net share settlement, the withheld shares are constructively retired and are not recorded as treasury stock. The par value of withheld shares reduces common stock, with the excess of fair value over par charged to additional paid-in capital. Cash paid to taxing authorities under net share settlement is classified as a financing activity in the condensed consolidated statement of cash flows.

2. Balance Sheet Information

Cash, Cash Equivalents and Restricted Cash

A summary of cash and cash equivalents and restricted cash is as follows:


	September 30, 2026		December 31, 2025
Cash and Cash Equivalents	$	5,570,640	$	8,696,570
Restricted Cash, Non-current	4,765		4,566
Total Cash, Cash Equivalents and Restricted Cash	$	5,575,405	$	8,701,136

Non-current restricted cash consists of deposits with financial institutions for corporate credit cards.

Short-term Investments

The following table summarizes short-term investments as of September 30, 2026 and December 31, 2025:


	As of September 30, 2026
			Unrealized
	Amortized Cost		Gains		Losses		Estimated Fair Value

Government Agency Securities	6,884,921		63		(12,122)		6,872,862
Corporate Debt Securities	3,852,283		—		(8,815)		3,843,469

Total Short-term Investments	$	10,737,204	$	63	$	(20,937)	$	10,716,331


	As of December 31, 2025
			Unrealized
	Amortized Cost		Gains		Losses		Estimated Fair Value

Government Agency Securities	$	5,171,407	$	4,633	$	—	$	5,176,040
Corporate Debt Securities	3,211,460		5,013		(1)		3,216,473

Total Short-term Investments	$	8,382,867	$	9,646	$	(1)	$	8,392,513

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KIORA PHARMACEUTICALS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (unaudited)

September 30, 2026

The following table summarizes the maturities of the Company's short-term investments at September 30, 2026 and December 31, 2025:


	As of September 30, 2026
	Amortized Cost		Estimated Fair Value
Due in one year or less	$	10,737,204	$	10,716,331

Total Short-term Investments	$	10,737,204	$	10,716,331


	As of December 31, 2025
	Amortized Cost		Estimated Fair Value
Due in one year or less	$	8,382,867	$	8,392,513

Total Short-term Investments	$	8,382,867	$	8,392,513

The following table shows the Company's available-for-sale investments' gross unrealized losses and fair value aggregated by investment category and length of time that individual securities have been in a continuous loss position, at September 30, 2026 and December 31, 2025:


	As of September 30, 2026
	Less than 12 months
	Count	Fair Value		Unrealized Losses

Government Agency Securities	21	$	6,244,373	$	(12,122)
Corporate Debt Securities	47	$	3,792,731	$	(8,815)

Total	68	$	10,037,105	$	(20,937)


	As of December 31, 2025
	Less than 12 months
	Count	Fair Value		Unrealized Losses


Corporate Debt Securities	1	$	76,056	$	(1)

Total	1	$	76,056	$	(1)

The Company reviews its investments each quarter to identify and evaluate investments that have an indication of possible other-than-temporary impairment. Factors considered in determining whether a loss is other-than-temporary include the length of time and extent to which fair value has been less than the cost basis, any changes to the underlying credit risk of the investment, and the Company’s intent and ability to hold the investment for a period of time sufficient to allow for any anticipated recovery in market value. The unrealized losses in the Company’s investments were caused by changes in interest rates resulting from changing economic conditions, and not from a decline in credit of their underlying issuers. The Company may be required to sell these investments prior to maturity to implement management strategies, however, it is not likely that the Company will sell these investments before recovery of their amortized cost basis. As such, the Company has classified these losses as temporary in nature.

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KIORA PHARMACEUTICALS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (unaudited)

September 30, 2026

Prepaid Expenses and Other Current Assets

Prepaid expenses and other current assets consist of the following:


	September 30, 2026		December 31, 2025
Prepaid Research and Development	$	782,524	$	841,723
Prepaid General and Administrative	132,347		211,501
Prepaid Insurance	93,951		88,580

Total Prepaid Expenses and Other Current Assets	$	1,008,822	$	1,141,804

Tax and Other Receivables

Tax and other receivables consist of the following:


	September 30, 2026		December 31, 2025
Income Tax Receivables	$	1,028,326	$	1,028,326
Research and Development Tax Credit Receivables	479,819		713,719
Other Tax Receivables	70,958		51,414
Total Tax and Other Receivables	$	1,579,103	$	1,793,459

Accrued Expenses

Accrued expenses consist of the following:


	September 30, 2026		December 31, 2025
Payroll and Benefits	$	853,145	$	1,275,602
Clinical Trials	997,935		821,648
Professional Fees	223,162		83,278
Income Tax	—		142,096
Other	73,321		84,107
Total Accrued Expenses	$	2,147,562	$	2,406,731

3. Fair Value Disclosures

Short-term Investments

The accounting guidance defines fair value, establishes a consistent framework for measuring fair value, and expands disclosure for each major asset and liability category measured at fair value on either a recurring or nonrecurring basis. Fair value is defined as the exchange price that would be received for an asset or paid to transfer a liability (an exit price) in the principal or most advantageous market for the asset or liability in an orderly transaction between market participants on the measurement date. As such, fair value is a market-based measurement that should be determined based on assumptions that market participants would use in pricing an asset or liability. As a basis for considering such assumptions, the accounting guidance establishes a three-tier fair value hierarchy, which prioritizes the inputs used in measuring fair value as follows:

Level 1 - Unadjusted quoted prices in active markets that are accessible at the measurement date for identical, unrestricted assets or liabilities.

Level 2 - Quoted prices for similar assets and liabilities in active markets, quoted prices in markets that are not active, or inputs which are observable, either directly or indirectly, for substantially the full term of the asset or liability.

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KIORA PHARMACEUTICALS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (unaudited)

September 30, 2026

Level 3 - Prices or valuation techniques that require inputs that are both significant to the fair value measurement and unobservable (i.e., supported by little or no market activity).

The following table summarizes the Company's financial instruments measured at fair value on a recurring basis as of September 30, 2026 and December 31, 2025.


			Fair Value Measurements at Reporting Date Using
			Quoted Prices in Active Markets for Identical Assets		Significant Other Observable Inputs		Significant Unobservable Inputs
As of September 30, 2026	Total		(Level 1)		(Level 2)		(Level 3)
Cash Equivalents:
Money Market Funds	$	1,948,319	$	1,948,319	$	—	$	—
US Treasury Securities	169,912		—		169,912		—

Total Cash Equivalents Measured at Fair Value	$	2,118,231	$	1,948,319	$	169,912	$	—

Short-term Investments:

Government Agency Securities	6,872,862		—		6,872,862		—
Corporate Debt Securities	3,843,469		—		3,843,469		—

Total Short-term Investments Measured at Fair Value	$	10,716,331	$	—	$	10,716,331	$	—

Total Assets Measured at Fair Value	$	12,834,562	$	1,948,319	$	10,886,242	$	—


			Fair Value Measurements at Reporting Date Using
			Quoted Prices in Active Markets for Identical Assets		Significant Other Observable Inputs		Significant Unobservable Inputs
As of December 31, 2025	Total		(Level 1)		(Level 2)		(Level 3)
Cash Equivalents:
Money Market Funds	$	6,797,446	$	6,797,446	$	—	$	—

Total Cash Equivalents Measured at Fair Value	$	6,797,446	$	6,797,446	$	—	$	—

Short-term Investments:

Government Agency Securities	$	5,176,040	$	—	$	5,176,040	$	—
Corporate Debt Securities	3,216,473		—		3,216,473		—

Total Short-term Investments Measured at Fair Value	$	8,392,513	$	—	$	8,392,513	$	—

Total Assets Measured at Fair Value	$	15,189,959	$	6,797,446	$	8,392,513	$	—

Contingent Consideration

In connection with historical acquisitions, additional consideration may be owed by the Company related to the achievement of certain milestones and such contingent consideration payments are required by U.S. GAAP to

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KIORA PHARMACEUTICALS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (unaudited)

September 30, 2026

be presented at fair value. The following table provides information for liabilities measured at fair value on a recurring basis using Level 3 inputs:


	September 30, 2026		December 31, 2025
Contingent Consideration:

Non-current	$	3,082,326	$	2,939,316
Total Contingent Consideration	$	3,082,326	$	2,939,316

The Company initially values contingent consideration related to business combinations using a probability-weighted calculation of potential payment scenarios discounted at rates reflective of the risks associated with the expected future cash flows for certain milestones. Key assumptions used to estimate the fair value of contingent consideration include projected financial information, market data and the probability and timing of achieving the specific milestones. After the initial valuation, the Company generally uses its best estimate to measure contingent consideration at each subsequent reporting period using the following unobservable Level 3 inputs:


	Valuation Technique	Unobservable Inputs	September 30, 2026		December 31, 2025
	Discounted cash flow	Payment discount rate	16.3	%	14.3	%
Bayon		Payment period	2027 - 2030		2027 - 2030
Panoptes		Payment period	2029 - 2031		2029 - 2031
Bayon		Probability of success for payment	25% - 45%		25% - 45%
Panoptes		Probability of success for payment	30% - 33%		30% - 33%

Significant changes in these assumptions could result in a significantly higher or lower fair value. The contingent consideration reported in the above table is adjusted quarterly based upon the passage of time or the anticipated success or failure of achieving certain milestones. The change in fair value of contingent consideration of $143.0 thousand for the nine months ended September 30, 2026, reflects the passage of time as expected milestone payment dates approach, partially offset by an increase in the discount rate from 14.3% to 16.3%. The change in fair value of contingent consideration is recorded within operating expenses on the accompanying condensed consolidated statements of operations and comprehensive loss. In October 2026, subsequent to entering into the KIO-401 License Agreement the Company decided to discontinue further research and development of KIO-104. The Company will evaluate the related $1.7 million reversal of contingent consideration liability in the fourth quarter of 2026 (see Note 13).

In-process R&D

The Company records in-process R&D projects acquired in asset acquisitions that have not reached technological feasibility and which have no alternative future use at estimated fair value. For in-process R&D projects acquired in business combinations, the Company capitalizes the in-process R&D project as an indefinite-lived intangible asset and evaluates this asset annually for impairment until the R&D process has been completed. Once the R&D process is complete, the Company amortizes the R&D asset over its remaining useful life.

ASC 350 allows an entity to first assess qualitative factors to determine whether events and circumstances indicate that it is more likely than not (that is, a likelihood of more than 50 percent) that an indefinite-lived intangible asset is impaired. If it is more likely than not that the asset is impaired, the entity must calculate the fair value of the asset and record an impairment charge if the carrying amount exceeds fair value. If an entity concludes that there is a less than 50 percent likelihood that the asset is impaired, no further action is required. An indefinite-lived intangible asset should be tested for impairment if events or changes in circumstances indicate that it is more likely than not that the asset is impaired. If such events or changes have occurred, a quantitative assessment is required.

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KIORA PHARMACEUTICALS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (unaudited)

September 30, 2026

If an entity bypasses the qualitative assessment or determines from its qualitative assessment that an indefinite-lived intangible asset is more likely than not impaired, a quantitative impairment test should be performed. The quantitative impairment test compares the fair value of an indefinite-lived intangible asset with the asset’s carrying amount. If the fair value of the indefinite-lived intangible asset is less than the carrying amount, an impairment loss should be recognized in an amount equal to the difference in accordance with ASC 350-30-35-19.

The Company values in-process R&D related to asset acquisitions using the Income Approach which measures the value of an asset by the present value of its future economic benefits. These benefits can include interest and principal payments, earnings, cost savings, tax deductions, or proceeds from its disposition. Value indications are developed by discounting expected cash flows at a rate of return that incorporates the risk-free rate for the use of funds, the expected rate of inflation, and risks associated with the particular investment. The selected discount rate is the Company's weighted average cost of capital, which provides an expected rate of return based on the Company's capital structure, market capitalization reconciliation, the required yield on the Company's equity, and the required yield on the interest-bearing debt of which there is currently none.

Management completed, with the assistance of a third-party valuation firm, a quantitative assessment of in-process R&D as of December 31, 2025, the Company's annual impairment test date, which includes the following unobservable Level 3 inputs:

Valuation Technique

Unobservable Inputs

Discount Rate

KIO-104

Multi-Period Excess Earnings Method

Probability of success for next development phase

17% to 36%

39.5

KIO-301

Multi-Period Excess Earnings Method

Probability of success for next development phase

23% to 43%

39.5

As of September 30, 2026, the Company assessed qualitative factors to determine whether events and circumstances indicate impairment, and concluded that it is not more likely than not that any assets are impaired.

4. Capital Stock

During August 2026, 648 warrant shares expired.

On April 6, 2026, the Company entered into a private placement for 438,471 shares of common stock, pre-funded warrants to purchase up to 1,527,711 shares of common stock, and accompanying Tranche A-1 and Tranche A-2 warrants to purchase up to an aggregate of 9,830,908 shares of common stock. The total net proceeds from the private placement were approximately $4.9 million.

The Tranche A-1 warrants are exercisable for up to 7,864,726 shares of common stock at an exercise price of $1.94 per share for an aggregate of up to approximately $15.3 million and will expire at the earlier of (i) 30 calendar days following the announcement of the Company entering into a definitive agreement for a strategic transaction by the Company that results in the material expansion of the potential commercial market opportunity of the Company's therapeutic assets (see Note 13) and (ii) nine months from the initial exercise date of April 6, 2026.

The Tranche A-2 warrants are exercisable for up to 1,966,181 shares of common stock at an exercise price of $1.94 per share for an aggregate of up to approximately $3.8 million and will expire at the earlier of (i) 30 days following the announcement of completed enrollment with respect to a Phase 3 clinical trial of an asset owned or licensed by the Company and (ii) four years from the initial exercise date of April 6, 2026.

During January 2026, 188,889 shares of common stock were issued upon the exercise of pre-funded warrants and 4,253 warrant shares expired.

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KIORA PHARMACEUTICALS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (unaudited)

September 30, 2026

During 2025, 661,581 shares of common stock were issued upon the exercise of pre-funded warrants and 56,301 shares of common stock were issued upon the exercise of Class C Warrants at $4.7079 per share for aggregate proceeds of approximately $0.3 million.

5. Warrants

The following is a summary of warrant activity for the Company’s equity-classified warrants for the nine months ended September 30, 2026:


	Number of Common Shares Issuable Upon Exercise of Outstanding Warrants	Weighted Average Exercise Price		Weighted Average Remaining Term in Years
Outstanding at December 31, 2025	6,671,570	$	7.73	3.67
Issued	11,358,619	$	1.68
Exercised	(188,889)	$	0.0009
Expired	(4,901)	$	1,769.29
Outstanding at September 30, 2026	17,836,399	$	3.47	2.34

6. Net Loss per Share - Basic and Diluted

Basic net loss per share is computed by dividing net loss available to common shareholders by the weighted-average number of common shares outstanding for the time period, which for basic net loss per share, does not include the weighted-average unvested restricted common stock that has been issued and is subject to forfeiture totaling 68,086 and 71,887 shares for the three months ended September 30, 2026 and 2025, respectively and 86,954 and 68,658 shares for the nine months ended September 30, 2026 and 2025, respectively.

Shares of common stock issuable upon exercise of the Company’s pre-funded warrants are included in the weighted-average number of common shares outstanding used to compute basic and diluted net (loss) income per share, because the pre-funded warrants are exercisable for nominal consideration per share at any time, with no vesting or other contingencies. The weighted-average shares outstanding include 1,938,822 and 1,407,201 shares underlying pre-funded warrants for the three and nine months ended September 30, 2026, respectively, and 928,249 and 1,038,139 shares for the three and nine months ended September 30, 2025, respectively. As of September 30, 2026 and 2025, pre-funded warrants to purchase 1,938,822 and 928,249 shares of common stock were outstanding.

Dilutive common equivalent shares consist of stock options, warrants, and preferred stock and are calculated using the treasury stock method, which assumes the repurchase of common shares at the average market price during the period. Under the treasury stock method, options and warrants will have a dilutive effect when the average price of common stock during the period exceeds the exercise price of options or warrants. Common equivalent shares do not qualify as participating securities. In periods where the Company records a net loss, unvested restricted common stock and potential common stock equivalents are not included in the calculation of diluted net loss per share as their effect would be anti-dilutive. The following is a summary of potentially dilutive

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September 30, 2026

securities excluded from the calculation of diluted net loss per share for the nine months ended September 30, 2026 and 2025:


	2026	2025
Common Stock Warrants, Excluding Pre-funded Warrants	15,897,577	5,738,238
Employee Stock Options	701,721	408,161
Restricted Stock	68,086	71,887
Preferred Stock, as Converted into Common Stock	42,426	42,426
Common Stock Reserved for Future Issuance	1,612,807	570,846
Total	18,322,617	6,831,558

7. Stock-Based Compensation

Equity Incentive Plans

The Company's Board of Directors (the "Board") adopted the 2014 Equity Incentive Plan (the "2014 Plan") and the Employee Stock Purchase Plan (the “ESPP”) and the Company's Stockholders approved the 2014 Plan and ESPP in February 2015. The Board subsequently adopted the 2024 Equity Incentive Plan (the "2024 Plan") and the Company's Stockholders approved the Plan in May 2024. Following adoption of the 2024 Plan, no further grants were made under the 2014 Plan. In May 2025, the Board determined that the potential future benefits of the ESPP were outweighed by the costs of its administration and terminated the ESPP effective as of April 30, 2025.

Consistent with the 2014 Plan, the 2024 Plan provides for the granting of stock options (incentive and nonqualified), restricted stock or other stock-based awards to employees, officers, directors, consultants, and advisors. The Board is responsible for administration of the 2024 Plan. The Company’s Board determines the term of each option, the option exercise price, the number of shares for which each option is granted and the rate at which each option is exercisable. Incentive stock options may be granted to any officer or employee at an exercise price per share of not less than the fair value per common share on the date of the grant (not less than 110% of fair value in the case of holders of more than 10% of the Company’s voting stock) and with a term not to exceed ten years from the date of the grant (five years for incentive stock options granted to holders of more than 10% of the Company’s voting stock). Nonqualified stock options may be granted to any officer, employee, consultant, or director at an exercise price per share of not less than the par value per share. In January 2026, the number of shares of common stock issuable under the 2024 Plan automatically increased by 150,469 shares pursuant to the terms of the 2024 Plan. In June 2026, following the annual shareholder meeting vote, the number of shares of Common Stock issuable under the 2024 Plan was increased by 1,500,000 shares. As of September 30, 2026, the maximum number of shares of Common Stock that may be issued pursuant to the 2024 Plan was 2,503,602, of which 1,612,807 shares were available for awards.

Stock-based compensation expense is presented in the same expense line items as cash compensation paid and for the three and nine months ended September 30, 2026 and 2025 is as follows:


	Three months ended September 30,				Nine months ended September 30,
	2026		2025		2026		2025
Research and Development	$	45,130	$	99,801	$	158,758	$	283,438
General and Administrative	141,066		154,596		346,258		382,350
Total Stock-Based Compensation Expense	$	186,196	$	254,397	$	505,016	$	665,788

Stock Options

The Company grants time-based stock options which generally vest one-third of the underlying shares on the one-year anniversary of the grant date and the remainder ratably over a 24-month period. The fair value of time-

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September 30, 2026

based stock options is determined using the Black-Scholes Option Pricing Model, with such value recognized as expense over the service period, which is typically three years, net of actual forfeitures. A summary of the Company's assumptions used in determining the fair value of the stock options granted during the nine months ended September 30, 2026 and 2025 is shown in the following table:


	Nine months ended September 30,
	2026		2025
Risk-Free Interest Rate	4.23	%	3.97	%
Expected Life (years)	6.08		6.00
Expected Stock Price Volatility	129.6	%	136.6	%
Expected Dividend Yield	—	%	—	%

The weighted-average grant date fair value of options granted for the nine months ended September 30, 2026 was $2.17. The expected term of the options granted is based on management's estimate. Expected volatility is based on the historical volatility of the Company’s common stock. The risk-free interest rate is determined based upon a constant U.S. Treasury security rate with a contractual life that approximates the expected term of the option. Unamortized compensation expense related to the options amounted to $0.7 million as of September 30, 2026 and is expected to be recognized over a weighted average period of approximately 1.66 years.

Following is a summary of stock option activity for the nine months ended September 30, 2026:


	Number of Options	Weighted- Average Exercise Price		Weighted- Average Remaining Term in Years
Outstanding at December 31, 2025	418,154	$	8.10	8.78
Granted	343,809	$	2.40
Expired	(29,155)	$	12.91
Forfeited	(31,087)	$	2.91
Outstanding at September 30, 2026	701,721	$	5.14	8.83
Exercisable and vested at September 30, 2026	293,685	$	8.76	7.99

The stock options outstanding and exercisable as of September 30, 2026 had $69.2 thousand aggregate intrinsic value. The aggregate intrinsic value is calculated as the difference between the exercise price of the underlying options and the market price of the Company’s common stock for options that had exercise prices lower than $2.56, the closing price of the Company’s stock on September 30, 2026.

Restricted Stock Awards

Restricted stock compensation expense is recognized over the vesting period, which is typically one-third of the underlying shares on the one-year anniversary of the grant date and the remainder ratably over a 24-month period. Unamortized compensation expense related to the restricted stock awards amounted to $0.1 million as

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NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (unaudited)

September 30, 2026

of September 30, 2026 and is expected to be recognized over a weighted average period of approximately 1.80 years. The following is a summary of restricted stock activity for the nine months ended September 30, 2026:


	Number of Units	Weighted- Average Grant Date Fair Value		Weighted- Average Remaining Term in Years
Non-vested Outstanding at December 31, 2025	70,985	$	4.12	1.86
Awarded	43,341	$	1.98
Released	(27,886)	$	5.18
Forfeited	(18,354)	$	3.18
Non-vested Outstanding at September 30, 2026	68,086	$	2.58	1.96

8. Collaboration Agreements

In August 2026, the Company entered into an exclusive license agreement (the “CKD Agreement”) with CKD. Under the CKD Agreement, the Company granted CKD an exclusive, royalty-bearing, sublicensable license to develop, manufacture and commercialize KIO-301 for the treatment of ophthalmic diseases in the Republic of Korea (the “CKD License”). CKD is responsible, at its own cost, for the development, regulatory approval and commercialization of KIO-301 in the Republic of Korea. The parties participate in a joint steering committee that coordinates development, regulatory, manufacturing and commercialization matters and exchange development data. CKD may terminate the CKD Agreement for convenience upon 90 days’ notice.

Under the CKD Agreement, the Company received a non-refundable upfront payment of $1.0 million and is eligible to receive additional funding upon the achievement of specified development, regulatory and cumulative net sales milestones, as well as royalties of net sales of KIO-301 in the Republic of Korea.

The Company concluded that the CKD Agreement is a collaborative arrangement within the scope of ASC 808 and that CKD is a customer with respect to the CKD License, which is accounted for under ASC 606. The Company identified one performance obligation, the CKD License together with the related know-how, data and right of reference, which was transferred to CKD upon execution of the CKD Agreement. The transaction price consists of the $1.0 million upfront payment. The development and regulatory milestones are fully constrained and excluded from the transaction price due to the inherent risks and uncertainties of drug development, and the sales milestones and royalties are excluded under the sales-based royalty exception in ASC 606-10-55-65. There is no significant financing component. Accordingly, the Company recognized $1.0 million of collaboration revenue during the three months ended September 30, 2026. Development and regulatory milestones will be recognized as revenue when it is probable that a significant reversal will not occur, and sales milestones and royalties will be recognized when the related sales occur.

The upfront payment was subject to Korean withholding tax of $165,000, which CKD withheld and remitted to the Korean tax authorities on the Company’s behalf. The withholding tax is recognized in the income tax provision for the three and nine months ended September 30, 2026. In addition, the Company incurred a sublicense fee of $60,000 payable to the Regents of the University of California, which was recognized as research and development expense during the three months ended September 30, 2026 because the related license was transferred at a point in time. Sublicense fees on future milestone payments will be expensed in the period the related revenue is recognized.

In May 2025, the Company entered into an exclusive option agreement (the "Option Agreement") with Senju Pharmaceutical Co., Ltd ("Senju"). Under the agreement, the Company granted Senju an exclusive option to obtain a license to the development and commercialization rights of KIO-301 for the treatment of ophthalmic diseases in certain key countries in Asia, including Japan and China. The Company concluded that the Option Agreement contains two material performance obligations, the Option and the future License. The Option was deemed a material right per ASC 606 and therefore a separate performance obligation. However, the Company also determined that the Option performance obligation is not capable of being distinct because it is interrelated to the future License Agreement. There is no financing component in the Option Agreement.

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September 30, 2026

The Option Agreement provides for a nonrefundable upfront payment of $1.25 million, which has been deferred and recorded the consideration as a contract liability within the deferred collaboration revenue on the condensed consolidated balance sheet. Revenue associated with the option fee will be recognized at the earlier of the exercise of the option or expiration of the option term.

Similarly, the associated contract costs specifically, sublicense fees, will be included in prepaid expenses and expensed when incurred, at the earlier of the exercise or expiration of the option.

In October 2026, the Company separately entered into the KIO-401 License Agreement with Senju, under which the Company in-licensed rights to KIO-401 (see Note 13). The KIO-401 License Agreement does not modify the Option Agreement, and the payments to Senju under the KIO-401 License Agreement are consideration for a distinct license of intellectual property and do not reduce the transaction price of the Option Agreement.

In January 2024, the Company entered into a strategic development and commercialization agreement ("License Agreement") with Théa Open Innovation ("TOI"), a sister company of the global ophthalmic specialty company Laboratoires Théa. Under the agreement, the Company granted TOI exclusive worldwide development and commercialization rights, excluding certain countries in Asia, to KIO-301 for the treatment of degenerative retinal diseases (the "License"). The Company concluded that the Licensing Agreement contains one material performance obligation, the License. The transaction price includes the upfront, non-refundable payment of $16.0 million (the "License Access Fee"). The Company did not include any development or regulatory milestones in the transaction price because it is probable that changes in the estimate of receiving those milestones would result in significant reversals of cumulative revenue in future periods, due to the inherent risks and uncertainties in the drug development process. The sales-based milestones and royalties are not included in the transaction price per ASC 606-10-32-11 and ASC 606-10-55-65. There is no financing component in the License Agreement.

The initial transaction price was allocated to the one performance obligation identified (the License), which was transferred to TOI at the execution of the License Agreement and the entire $16.0 million transaction price was recognized in the first quarter of 2024 upon the satisfaction of the license performance obligations. Variable components of consideration related to development and regulatory milestones, commercial milestones, and royalties will be allocated to the transaction price if and when they occur. When it is probable that including milestones in the transaction price will not result in significant reversals of cumulative revenue in future periods, the Company will recognize the revenue for the milestones immediately since the license performance obligation to which the milestones relate has already been fully satisfied when the change in estimate of the variable consideration occurs. Since the reimbursement for the development activities clearly relates to those activities and are accounted for under ASC 808, the Company will recognize those amounts that are due from TOI as contra-R&D expense.

The License Access Fee was earned at a point in time (first quarter of 2024) and, as a result, the associated contract costs specifically, sublicense fees, were expensed at the same point in time (first quarter of 2024). All further revenue sources that may lead to sublicense fee payments will not be recognized until earned. As such, sublicense fees will be expensed in the same period as the revenue of the respective milestone or royalties are earned.

9. Commitments and Contingencies

Leases

The Company is party to six real property operating leases for the rental of office and clinical trial space.

Clinical Trial Site Leases

In February 2026, the Company entered into a lease in Auckland City, New Zealand (the "New Zealand Lease") that commenced in March 2026 with a term of 2 years with an option to extend for 2 additional years to support the ABACUS-2 clinical trial. Terms include monthly rent payments of approximately $2.2 thousand, adjusting annually based on CPI and a security deposit of $21.8 thousand. The Company recorded a ROU asset and lease liability, with a term of 2 years, ending in February 2028.

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September 30, 2026

In January 2025, the Company entered into a lease in Perth, Australia (the "Perth Lease") and another in Brisbane, Australia (the "Brisbane Lease"). Both leases commenced in February 2025, at which time the Company recorded a ROU asset and lease liability, with a term of 2 years through January 2027 to support the ABACUS-2 clinical trial. Monthly rent payments are approximately $6.0 thousand, and the total security deposit is $32.2 thousand. The Company has rent abatement for the first 2 months of the Brisbane Lease and for the first 3 months of the Perth Lease.

The Brisbane, Perth, and New Zealand leases are for ABACUS-2 clinical trial sites, with rent costs fully reimbursed by TOI.

In May 2022, the Company entered into a 12-month lease for office space in Adelaide, Australia (the "Adelaide Lease") which expired in May 2023. Following expiration, the landlord agreed to extend the Adelaide Lease on a month-month basis, whereby the Company must provide 90-day notice of termination. The Adelaide Lease is a short-term lease which is exempt for ROU asset and lease liability reporting. Monthly rent payments are approximately $1.5 thousand. The Adelaide lease is being used as a clinical trial site for ABACUS-2, with rent costs fully reimbursed by TOI.

Corporate Leases

In March 2025, the Company entered into a new lease in Encinitas, California (the "New Encinitas Lease") which is the current headquarters for the Company. The New Encinitas Lease commenced in June 2025 with a term of 3 years and 3 months through August 31, 2028. Monthly rent payments are approximately $8.4 thousand per month and will increase by approximately 4% each year on the anniversary of the lease commencement, starting in 2026. The Company has rent abatement for 3 months of the lease in the form of half rent in months two, three, four, five, thirteen and fourteen, and maintains a security deposit of $9.4 thousand. The Company received $72.8 thousand from the lessor for tenant improvements.

The Company also entered into a lease for office space in Vienna, Austria (the "Vienna Lease"). The Vienna Lease commenced on October 15, 2023 with a term of 5 years through October 14, 2028. The Company recorded a ROU asset and lease liability upon lease commencement in October 2023. Monthly rent payments are approximately $1.3 thousand, and the security deposit is $5.3 thousand.

Operating lease expense, consisting of the reduction of the right-of-use asset and the imputed interest on the lease liability, totaled $65.4 thousand and $50.2 thousand for the three months ended September 30, 2026 and 2025, respectively, and $188.1 thousand and $116.7 thousand for the nine months ended September 30, 2026 and 2025, respectively. The remaining lease terms range from less than 0.3 years to 2.1 years.

Supplemental balance sheet information related to the leases is as follows as of September 30, 2026:


Weighted-Average Remaining Lease Term	1.7 years
Weighted-Average Discount Rate	5.94	%

Future annual minimum lease payments under non-cancellable operating leases as of September 30, 2026 are as follows:


Years Ending December 31,
2026 (remaining months)	$	55,502
2027	155,908
2028	89,921


Total Lease Liabilities	301,331
Less Amounts Representing Interest	(14,542)
Total	286,789
Less Current Portion	(162,095)
	$	124,694

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NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (unaudited)

September 30, 2026

Option Agreements

The Company is party to one option agreement, the details of which have been previously disclosed in Note 12 to the consolidated financial statements in the Company's Annual Report on Form 10-K for the year ended December 31, 2025. There have been no material changes to the terms of this agreement during the nine months ended September 30, 2026.

License and Exclusive Rights Agreements

The Company is a party to six license agreements, the details of which have been previously disclosed in Note 12 to the consolidated financial statements in the Company's Annual Report on Form 10-K for the year ended December 31, 2025. There have been no material changes to the terms of these agreements during the nine months ended September 30, 2026.

Contingent Consideration

The purchase price of various acquisitions in prior periods included contingent consideration, which consisted of various earn-out payments payable in cash or shares upon the achievement of certain milestones. Below are the maximum obligation payments per the respective agreements and estimated fair value of contingent consideration payments remaining as of September 30, 2026.


	Maximum Obligation per Agreements		Current Fair Value Estimated
Bayon	$	7,135,000	$	1,341,780
Panoptes	9,500,000		1,740,546
	$	16,635,000	$	3,082,326

Credit Line Agreement

In March 2025, the Company entered into a credit line with UBS (the “Credit Line”) providing for a $10.0 million revolving line of credit. The Credit Line bears interest at the 30-day Secured Overnight Financing Rate ("SOFR") average, plus 1.5%. The SOFR rate is variable. The Credit Line is secured by a first priority lien and security interest in the Company’s marketable securities held in its managed investment accounts with UBS. During 2025, the Company received $2.8 million in proceeds from the line, and made payments of $2.8 million. There were no borrowings during the quarter resulting in no credit balance as of September 30, 2026.

Other

In the normal course of business, the Company periodically becomes involved in various claims and lawsuits, as well as governmental proceedings and investigations that are incidental to the business. The Company accrues a liability when a loss is considered probable and the amount can be reasonably estimated. When a material loss contingency is reasonably possible but not probable, the Company does not record a liability, but instead discloses the nature and amount of the claim, and an estimate of the possible loss or range of loss, if such an estimate can be made. Legal fees are expensed as incurred. With respect to governmental proceedings and investigations, like other companies in the industry, the Company is subject to extensive regulation by national, state and local governmental agencies in the U.S. and in other jurisdictions in which the Company and its affiliates operate. As a result, interaction with governmental agencies is ongoing. The Company’s standard practice is to cooperate with regulators and investigators in responding to inquiries.

The Company currently maintains insurance for risks associated with the operation of its business, provision of professional services and ownership of property. These policies provide coverage for a variety of potential losses, including loss or damage to property, bodily injury, general commercial liability, professional errors and omissions and medical malpractice.

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September 30, 2026

10. Segment Information

The Company operates in and reports as a single reportable segment, focused on the development of innovative ophthalmic pharmaceutical products.

Our Chief Operating Decision Maker "CODM" is our President and Chief Executive Officer. The CODM does not evaluate profitability nor evaluate performance or allocate resources below the level of the consolidated Company. The accounting policies of the segment are the same as those described in the summary of significant accounting policies. The CODM reviews operating expenses and net loss presented on a consolidated basis for purposes of allocating resources and evaluating financial performance. These metrics serve as benchmarks to evaluate the business, measure performance, identify trends, prepare financial projections, and make strategic decisions. The CODM does not evaluate performance or allocate resources based on segment assets data; therefore, total segment assets are not presented.

The following table presents the revenue, significant expenses, and net loss for the Company’s single reportable segment:


	Three Months Ended September 30,				Nine Months Ended September 30,
	2026		2025		2026		2025
Total Revenue	$	1,000,000	$	—	$	1,000,000	$	—
Significant and Other Segment Expenses
General and Administrative	$	1,580,111	$	1,443,827	4,575,882		4,287,075
Research and Development
KIO-101	—		11,223		—		18,017
KIO-1041	176,392		255,085		730,557		532,106
KIO-301	1,353,489		2,057,678		4,662,355		6,285,162
Unallocated R&D Expenses2	419,983		405,905		757,793		1,016,981
Total Research & Development	1,949,864		2,729,891		6,150,705		7,852,266
KIO-301 Collaboration Credit	(885,559)		(1,658,248)		(3,455,046)		(5,310,288)


Change in Fair Value of Contingent Consideration	46,169		(1,721,033)		143,010		(1,308,067)
Interest Income, Net	(146,306)		(201,822)		(431,876)		(703,692)
Other Segment Expenses3	40,242		23,708		98,040		133,517
Income Tax Expense (Benefit)	165,000		(643,129)		165,800		(632,179)
Net Loss	$	(1,749,521)	$	26,806	$	(6,246,515)	$	(4,318,633)

1 Net of research tax credit offset.

2 Unallocated research and development expenses primarily include personnel costs, research consulting and scientific advisory expenses.

3 Other segment expenses primarily include interest expense, other income, net, and loss on disposal of fixed assets.

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NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (unaudited)

September 30, 2026

11. Prepaid Collaboration Expenses

The "Prepaid Collaboration Expenses" asset on the condensed consolidated balance sheets represents the cumulative amount of: (i) Deferred Collaboration Credits, which are prepaid R&D expenses that are eligible for reimbursement but for which the related services have not yet been provided to the Company and are currently recognized as “Collaboration Credit” on the condensed consolidated statements of operations and comprehensive loss as the expenses are incurred, (ii) Accrued Expense Adjustments, which are research and development ("R&D") expenses that have been incurred but have not yet been invoiced by a third-party vendor and thereby are not yet paid/submitted for reimbursement, and (iii) Value Added Tax on R&D expense to be refunded to the Company and repaid to TOI. The changes in these balances have been included in the table in Note 12 for reference in reconciling the Amount Billed/Submitted for Reimbursement compared to the amount of R&D Expenses Incurred.


	Three Months Ended September 30,				Nine Months Ended September 30,
	2026		2025		2026		2025
Beginning Balance	$	390,042	$	(219,625)	$	201,332	$	(981,111)
Change in prepaid expenses included in TOI reimbursement	37,940		10,015		58,276		424,596
Change in prepaid expenses invoiced to other collaboration partners	(13,646)		—		(13,646)		—
Accrued expenses for work performed, not yet invoiced	104,447		179,141		138,745		521,402
Taxes received and repaid	(124,254)		—		—		—
Foreign currency adjustments	7,908		1,412		17,730		6,056
Ending Balance	$	402,437	$	(29,057)	$	402,437	$	(29,057)

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NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (unaudited)

September 30, 2026

12. Roll-forward of TOI Activity

Per the terms of the license and collaboration agreement with TOI, TOI is responsible for all R&D expenses related to KIO-301. This provides for the Company's right to reimbursement upon its submission to TOI of an allowable vendor invoice. Allowable vendor invoices that the Company receives may pertain to services already rendered to the Company, while others may pertain to the prepayment of services that the Company will receive in future periods.

The table below summarizes the R&D expenses submitted for reimbursement and the R&D expenses incurred by the Company related to the collaboration, including the corresponding collaboration credits. These amounts are presented for the most recent relevant periods:


Period	Amount Billed/ Submitted for Reimbursement			Amount Reimbursed/ Received			R&D Expenses Incurred		Collaboration Credits		Variance (foreign exchange timing)		Adjustment to Deferred Collaboration Credits4		Adjustment to Accrued Expenses5





Quarter ended March 31, 2025	$	1,727,386	6	$	(990,979)	7	$	1,969,270	$	(1,966,123)	$	(3,147)	$	251,304	$	(9,420)
Quarter ended June 30, 2025	$	1,168,022		$	(1,337,604)		$	1,682,980	$	(1,685,917)	$	2,937	$	163,277	$	351,681
Quarter ended September 30, 2025	$	1,467,935	8	$	(1,422,731)		$	1,657,091	$	(1,658,248)	$	1,117	$	10,015	$	179,141
Quarter ended December 31, 2025	$	1,522,770		$	(1,213,226)		$	1,752,591	$	(1,755,950)	$	3,359	$	238,264	$	(8,443)
Fiscal Year ended December 31, 2025	$	5,886,113		$	(4,964,540)		$	7,061,932	$	(7,066,238)	$	4,266	$	662,860	$	512,959
Quarter ended March 31, 2026	$	1,544,253		$	(1,522,770)		$	1,234,646	$	(1,233,224)	$	(1,422)	$	(55,395)	$	(254,212)
Quarter ended June 30, 2026	$	1,091,385		$	(1,544,253)		$	1,343,316	$	(1,336,263)	$	(7,053)	$	75,731	$	176,200
Quarter ended September 30, 2026	735,419			(1,091,385)			877,806		(885,559)		7,752		37,940		104,447

4 Change in prepaid expenses that have not yet been incurred but which have been paid/submitted for reimbursement. The Company's contract with TOI allows for reimbursement upon the Company's receipt of an allowable vendor invoice.

5 Change in expenses incurred but not billable to TOI until invoiced by a third-party vendor and other taxes receivable to be repaid to TOI.

6 Includes $389,782 billed in February 2025 related to Phase 3 activities that were reimbursed by TOI prior to quarter-end March 31, 2025, plus $1,337,604 related to reimbursable first quarter 2025 R&D expenses, subsequently reimbursed in the second quarter of 2025.

7 Includes $601,197 related to fourth quarter 2024 Collaboration Receivable and $389,782 billed and reimbursed by TOI in February 2025.

8 Includes $254,709 billed in August 2025 related to Phase 3 activities that were reimbursed by TOI prior to quarter-end September 30, 2025, plus $1,213,226 related to reimbursable third quarter 2025 R&D expenses, subsequently reimbursed in the fourth quarter of 2025.

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NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (unaudited)

September 30, 2026

13. Subsequent Events

The Company has evaluated subsequent events through the date on which these condensed consolidated financial statements were available to be issued.

KIO-401 License Agreement with Senju

On October 23, 2026, the Company entered into the KIO-401 License Agreement with Senju. Under the agreement, the Company obtained exclusive rights to develop, manufacture and commercialize KIO-401 (designated by Senju as SNJ-1945) in the field of ophthalmology in North America, South America, Europe, the Middle East and Africa (the “KIO-401 Territory”). KIO-401 is an oral small-molecule inhibitor of activated calpain. The Company also holds a right of first refusal for Australia and New Zealand, and the KIO-401 Territory will expand automatically to include those countries if neither Senju nor a Senju licensee files for regulatory approval there within a specified period after the Company’s first NDA filing.

Senju completed Phase 2 and Phase 3 clinical trials of KIO-401 in patients with central retinal artery occlusion (“CRAO”) in Japan. The Company plans to initiate a global Phase 3 registration trial in CRAO and a Phase 2b clinical trial in non-arteritic anterior ischemic optic neuropathy ("NAION").

Under the KIO-401 License Agreement, the Company will:

•pay Senju an upfront payment of $3.5 million;

•be obligated to pay $12.5 million upon receipt of Senju's initial technology transfer package, which is partially creditable against future royalties;

•be obligated to pay development, regulatory, and commercial milestone payments upon the achievement of specified milestones;

•pay flat-rate royalties in the single digits on net sales of licensed products outside of Asia.

The Company expects to account for the transaction as an asset acquisition. KIO-401 has not received regulatory approval in the Company’s territory and has no alternative future use, so the Company expects to recognize the upfront payment as research and development expense in the fourth quarter of 2026. The technology transfer milestone will be recognized as research and development expense when the technology transfer package is received. Other milestone payments will be recognized when the related milestone is probable and reasonably estimable.

Senju is also the counterparty to the KIO-301 Option Agreement described in Note 8. The KIO-401 License Agreement does not modify the KIO-301 Option Agreement, and the $1.25 million option fee remains deferred as of September 30, 2026.

Discontinuation of KIO-104 Development

In connection with the KIO-401 License Agreement, and to prioritize investment in KIO-401 and its later-stage retinal programs, the Company decided in October 2026 to discontinue further research and development of KIO-104. The decision was not based on safety or efficacy findings. The Company will report data from patients enrolled in the KLARITY clinical trial and is willing to consider partnering or out-licensing opportunities for the asset.

As of September 30, 2026, the carrying value of the in-process research and development asset associated with the KIO-104 program was $1.0 million. The discontinuation is an indicator of impairment, and the Company will evaluate the asset for impairment in the fourth quarter of 2026. This evaluation could result in an impairment charge of up to the full $1.0 million carrying value. Management will also consider the discontinuation of KIO-104 in its prospective fair value estimations related to contingent consideration which could result in reversal of the full $1.7 million of liabilities.

April 2026 Tranche A-1 warrants

The Tranche A-1 warrants issued in the April 2026 private placement, which are exercisable for up to 7,864,726 shares of common stock at $1.94 per share, expire on the earlier of 30 days after the Company announces a

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KIORA PHARMACEUTICALS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (unaudited)

September 30, 2026

definitive agreement for a strategic transaction that materially expands the potential commercial market opportunity of its therapeutic assets and January 6, 2027. The announcement of the KIO-401 License Agreement on October 29, 2026 satisfied this condition; accordingly, the Tranche A-1 warrants will expire on November 28, 2026 unless exercised.

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Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations.

The following section of this Quarterly Report on Form 10-Q entitled “Management’s Discussion and Analysis of Financial Condition and Results of Operations” contains statements that are not statements of historical fact and are forward-looking statements within the meaning of federal securities laws. These statements involve known and unknown risks, uncertainties and other factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. These statements reflect our current views with respect to future events and are based on assumptions and subject to risks and uncertainties. Factors that may cause our actual results to differ materially from those in the forward-looking statements include those factors described in “Item 1A. Risk Factors” beginning on page 21 of our Annual Report on Form 10-K for the fiscal year ended December 31, 2025 as filed with the Securities and Exchange Commission on March 25, 2026. You should carefully review all of these factors, as well as the comprehensive discussion of forward-looking statements on page 1 of this Quarterly Report on Form 10-Q.

Kiora Pharmaceuticals, Inc. is referred to herein as “Kiora”, “we,” “our,” “us,” and “the Company”.

Executive Summary

We are a clinical-stage, specialty pharmaceutical company developing and commercializing products for the treatment of ophthalmic diseases.

In October 2026, we entered into an exclusive license agreement with Senju to develop and commercialize KIO-401, an oral small-molecule calpain inhibitor, in ophthalmology in North America, South America, Europe, the Middle East and Africa. Senju completed Phase 2 and Phase 3 clinical trials of KIO-401 in patients with central retinal artery occlusion (“CRAO”) in Japan, and we plan to initiate a global Phase 3 registration trial in CRAO in 2027 and a Phase 2b clinical trial in non-arteritic anterior ischemic optic neuropathy (“NAION”). We will pay Senju a $3.5 million upfront payment and may pay additional technology transfer, regulatory, commercial launch and sales milestones and royalties on net sales.

KIO-301 is initially focused on patients with later stages of disease progression due to retinitis pigmentosa (any and all sub-forms). KIO-301 is a potential vision-restoring small molecule that acts as a “photoswitch” specifically designed to restore vision in patients with inherited and age-related degenerative retinal diseases. The molecule is specifically designed to restore the eyes’ ability to perceive and interpret light in visually impaired patients. It selectively enters viable downstream retinal ganglion cells (no longer receiving electrical input due to degenerated rods and cones) and is intended to turn them into light sensing cells, capable of signaling the brain as to the presence or absence of light. On March 17, 2022, we were granted Orphan Drug Designation by the United States (“U.S.”) Food and Drug Administration (“FDA”) for the Active Pharmaceutical Ingredient (“API”) in KIO-301. In July 2024, we were granted Orphan Medicinal Product Designation by the European Medicines Agency for KIO-301 for the treatment of non-syndromic, rod-dominant retinal dystrophies, which includes diseases like retinitis pigmentosa, choroideremia, Stargardt disease and others. In September 2024, the European Medicines Agency expanded our Orphan Medicinal Product Designation to also include syndromic, rod-dominant retinal dystrophies that includes diseases like Usher's syndrome, which has non-ocular aspects of diseases in addition to retinal involvement.

KIO-301 was acquired through the Bayon Therapeutics, Inc. ("Bayon") transaction that closed October 21, 2021. We initiated a Phase 1b clinical trial ("ABACUS-1") in the third quarter of 2022. Topline data from this trial was presented at the American Academy of Ophthalmology annual meeting in November 2023. The complete data set was presented at the Association for Research in Vision and Ophthalmology ("ARVO") annual conference in May 2024 highlighting improvements in visual acuity, visual field and functional vision among clinical trial participants relative to baseline.

In January 2024, we entered into a strategic development and commercialization agreement ("License Agreement") with Théa Open Innovation ("TOI"), a sister company of the global ophthalmic specialty company Laboratoires Théa. Under the agreement, Kiora granted TOI exclusive worldwide development and commercialization rights, excluding Asia, to KIO-301 for the treatment of degenerative retinal diseases. In exchange, Kiora received an upfront, payment of $16 million; up to $285 million upon achievement of pre-specified clinical development, regulatory and commercial milestones; tiered royalties of up to low 20% on net

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sales; and reimbursement of all KIO-301 research and development expenses moving forward from the date of the execution of the License Agreement.

In October 2024, we, in collaboration with our partner TOI, announced that we received regulatory approval to initiate a Phase 2 clinical trial to investigate KIO-301 for vision restoration in patients with retinitis pigmentosa. The ABACUS-2 trial is expected be a 36 patient, multi-center, double-masked, randomized, controlled, multiple dose study enrolling patients with ultra-low vision or no light perception regardless of their underlying gene mutation associated with retinitis pigmentosa. Enrollment began in the second quarter of 2025 and dosing began in the third quarter of 2025.

Based on results of ABACUS-1, we have the opportunity to expand development of KIO-301 to treat patients with late stages of Choroideremia and Stargardt disease. These diseases have a similar underlying late-stage pathology as Retinitis Pigmentosa, hence the mechanism of action of KIO-301 could potentially provide a similar benefit to these patients.

In May 2025, we entered into an exclusive option agreement with Senju Pharmaceutical Co., Ltd ("Senju"). Under the agreement, we granted Senju an exclusive option to obtain an exclusive license to the development and commercialization rights of KIO-301 for the treatment of ophthalmic diseases in certain key countries in Asia, including Japan and China. In exchange, we received a nonrefundable payment of $1.25 million. In the future, if the option is exercised and a license agreement is executed, we will be eligible to receive an additional $109.5 million plus tiered royalties of up to high teen percentages on net sales.

In August 2026, we entered into an exclusive license agreement with Chong Kun Dang Pharmaceutical Corporation (“CKD”). Under the agreement, we granted CKD exclusive rights to develop and commercialize KIO-301 for the treatment of ophthalmic diseases in the Republic of Korea. In exchange, we received an upfront payment of $1.0 million and are eligible to receive up to $15.5 million upon the achievement of specified development, regulatory and sales milestones, plus royalties of 10% on net sales in the Republic of Korea. CKD is responsible for the development, regulatory and commercialization activities and costs in the Republic of Korea, and the parties coordinate through a joint steering committee.

In October 2026, to prioritize investment in KIO-401 and our later-stage retinal programs, we discontinued further research and development of KIO-104. We will report data from patients enrolled in the KLARITY clinical trial and intend to pursue partnering or out-licensing opportunities for KIO-104. As of September 30, 2026, we were developing KIO-104 for the treatment of retinal inflammatory diseases including Posterior Non-Infectious Uveitis, a rare T cell-mediated, intraocular inflammatory disease and diabetic macular edema. KIO-104 is a novel and potent small molecule inhibitor of dihydroorotate dehydrogenase ("DHODH"), formulated for intravitreal delivery and ideally suited to suppress overactive T-cell activity to treat the underlying condition. Data from a previous Phase 1/2a study in patients with Posterior Non-Infectious Uveitis, reported in October 2022, showed that a single injection of KIO-104 decreased intraocular inflammation and improved visual acuity significantly for the duration of the study. Further, KIO-104 reduced macular edema (swelling) which if unchecked, can lead to permanent vision loss. The drug was well tolerated, with no serious side effects on intraocular tissues or other serious adverse events observed. In May 2025, we received approval to start enrolling patients in a Phase 2 trial for KIO-104 in retinal inflammation and began enrollment in the second quarter of 2025. Dosing began in the third quarter of 2025.

We have an additional asset, KIO-101, that is currently available to partner. KIO-101 is based on the same molecule as KIO-104, however formulated for topical, eye drop delivery.

Throughout our history we have not generated significant revenue; however, in January 2024 we entered into the License Agreement with TOI, whereby we recognized $16 million in collaboration revenue related to the upfront payment and in August 2026 we entered into the license agreement with CKD, whereby we recognized $1.0 million in collaboration revenue related to the upfront payment. With the exception of the year ended December 31, 2024, Kiora has incurred annual losses and negative cash flows since inception, and future losses are anticipated. From inception through September 30, 2026, our losses have aggregated $160.5 million. We expect to incur significant expenses and increasing operating losses for the foreseeable future as we continue the development and clinical trials of and seek regulatory approval for our product candidates. If we obtain regulatory approval for our product candidates, we expect to incur significant expenses in order to create an infrastructure to support their commercialization including sales, marketing, and distribution functions.

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We will need additional financing to support our continuing operations. We will seek to fund our operations through a combination of public or private sales of equity, debt financings, license and development agreements, non-dilutive grants and other sources, which may include collaborations with third parties. Adequate additional financing may not be available to us on acceptable terms, or at all. Our failure to raise capital as and when needed would have a negative impact on our financial condition and our ability to pursue our business strategy. Although historically we have been successful at raising capital, additional capital may not be available on terms favorable to Kiora, if at all. We do not know if any future offerings will succeed. Our failure to raise capital as and when needed would have a negative impact on our financial condition and our ability to pursue our business strategy. These conditions raise substantial doubt about our ability to continue as a going concern. We will need to generate significant revenue to achieve profitability, and we may never do so.

Recent Developments

Subsequent to September 30, 2026, we entered into the KIO-401 License Agreement with Senju and discontinued further development of KIO-104, as described in the Executive Summary above and in Note 13, Subsequent Events, to the condensed consolidated financial statements.

New Components of Results of Operations

Collaboration Revenue. Collaboration revenue consists of revenue recognized under ASC 606 for licenses of our intellectual property to collaboration partners that are customers, including upfront payments and, when no longer constrained, milestone payments and royalties. For the three and nine months ended September 30, 2026, collaboration revenue consisted of the $1.0 million upfront payment under the CKD license agreement.

Results of Operations

Comparison of three months ended September 30, 2026 and 2025

The following table summarizes the results of our operations for the three months ended September 30, 2026 and 2025:


	2026		2025		Change
Revenue:
Collaboration Revenue	$	1,000,000	$	—	$	1,000,000

Total Revenue	1,000,000		—		1,000,000
Operating Expenses:
General and Administrative	$	1,580,111	$	1,443,827	$	136,284
Research and Development	1,949,864		2,729,891		(780,027)
Collaboration and Research Credits	(885,559)		(1,658,248)		772,689

Change in Fair Value of Contingent Consideration	46,169		(1,721,033)		1,767,202
Total Operating Expenses	2,690,585		794,437		1,896,148
Other Income, Net	106,064		178,114		(72,050)
Loss Before Income Tax (Expense) Benefit	(1,584,521)		(616,323)		(968,198)
Income Tax (Expense) Benefit	(165,000)		643,129		(808,129)
Net (Loss) Income	$	(1,749,521)	$	26,806	$	(1,776,327)

Collaboration Revenue. Collaboration revenue of $1.0 million for the three and nine months ended September 30, 2026 relates to the upfront payment under the CKD license agreement, which was recognized upon the transfer of the license in August 2026. There was no collaboration revenue in the comparable periods of 2025.

General and Administrative Expenses. The increase of $136.3 thousand was driven primarily by higher professional services.

Research and Development Expenses. The decrease of $0.8 million was primarily due to a decrease in preclinical and CMC related expenses of $0.7 million and $0.1 million lower personnel costs related to transition

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timing of key personnel. The change also includes a $60,000 sublicense fee owed to the Regents of the University of California in connection with the CKD license agreement.

Collaboration and Research Credits. The decrease of $0.8 million is related to decreased research and development expenses for the KIO-301 program which are fully reimbursed by TOI.

Change in Fair Value of Contingent Consideration. The decrease of $1.8 million primarily driven by an increased discount period and changes to the development plan as discussed in Note 3, Fair Value Disclosures - Contingent Consideration, to the Notes to the Consolidated Financial Statements of Part IV, Item 16. Form 10-K as of December 31, 2025.

Income Tax Provision. The decrease of $0.8 million is due to a change in estimate for 2024 tax year resulting from new legislation included in the One Big Beautiful Bill Act (OBBBA) realized in 2025. The income tax provision of $165,000 for the three months ended September 30, 2026 reflects Korean withholding tax on the upfront payment under the CKD license agreement.

Comparison of nine months ended, September 30, 2026 and 2025

The following table summarizes the results of our operations for the nine months ended September 30, 2026 and 2025:


	2026		2025		Change
Revenue:
Collaboration Revenue	$	1,000,000	$	—	$	1,000,000

Total Revenue	1,000,000		—		1,000,000
Operating Expenses:
General and Administrative	$	4,575,882	$	4,287,075	$	288,807
Research and Development	6,150,705		7,852,267		(1,701,562)
Collaboration Credits	(3,455,046)		(5,310,288)		1,855,242

Change in Fair Value of Contingent Consideration	143,010		(1,308,067)		1,451,077
Total Operating Expenses	7,414,551		5,520,987		1,893,564
Other Income, Net	333,836		570,175		(236,339)
Loss Before Income Tax (Expense) Benefit	(6,080,715)		(4,950,812)		(1,129,903)
Income Tax (Expense) Benefit	(165,800)		632,179		(797,979)
Net Loss	$	(6,246,515)	$	(4,318,633)	$	(1,927,882)

General and Administrative Expenses. The increase of $0.3 million was primarily due to increased professional services expenses driven by patent related legal expenses.

Research and Development Expenses. The decrease of $1.7 million was primarily due to lower preclinical and CMC expenses of $2.5 million, and research activities of $0.2 million partially offset by increased clinical trial activities of $0.9 million. The change also includes a $60,000 sublicense fee owed to the Regents of the University of California in connection with the CKD license agreement.

Collaboration and Research Credits. The decrease of $1.9 million is related to decreased research and development expenses for the KIO-301 program which are fully reimbursed by TOI.

Change in Fair Value of Contingent Consideration. The decrease of $1.5 million was primarily driven by an increased discount period and changes to the development plan as discussed in Note 3, Fair Value Disclosures - Contingent Consideration Commitments and Contingencies, to the Notes to the Condensed Consolidated Financial Statements of Part 1, Item 1. Financial Statements of this Form 10-Q.

Other Income, Net. The decrease of $0.2 million was primarily due to lower interest income resulting from lower interest rates and a lower carrying balance of short-term marketable securities.

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Liquidity and Capital Resources

Our principal liquidity needs have historically been for acquisitions, working capital, research and development, and capital expenditures. While we anticipate having sufficient cash to fund currently planned operations into late 2027, excluding the technology transfer milestone, we will need additional financing to support our future operations as we develop and work toward the commercialization of new products. We will seek to fund our operations through a combination of public or private sales of equity, debt financings, license and development agreements, non-dilutive grants and other sources, which may include collaborations with third parties.

If we raise additional funds by issuing equity securities or convertible debt, our stockholders will experience dilution. Debt financing through our $10 million credit line with UBS would result in increased fixed payment obligations and may involve agreements that include covenants limiting or restricting our ability to take specific actions, such as incurring additional debt, or making capital expenditures. If we raise additional funds through collaboration and licensing arrangements with third parties, it may be necessary to relinquish valuable rights to our products, future revenue streams or product candidates, or to grant licenses on terms that may not be favorable to us. Although historically we have been successful at raising capital, additional capital may not be available on terms favorable to us, if at all. We do not know if any future offerings will succeed. Our failure to raise capital as and when needed would have a negative impact on our financial condition and our ability to pursue our business strategy. We have incurred losses and negative cash flows since inception, and future losses are anticipated. Based on the cash on hand and short-term investments at September 30, 2026 of approximately $5.6 million and $10.7 million, respectively, the near term payment of $3.5 million due to Senju under the KIO-401 License Agreement and all KIO-301 expenses reimbursed by our partner TOI, we anticipate having sufficient cash to fund currently planned operations into late 2027, excluding the technology transfer milestone, which may become payable prior to such date. These conditions raise substantial doubt about our ability to continue as a going concern. We will need to generate significant revenue to achieve profitability, and we may never do so.

Information Regarding Cash Flows

In September 2026, we received $835,000 from CKD, representing the $1.0 million upfront payment net of $165,000 of Korean withholding tax. As of September 30, 2026, we had unrestricted cash and cash equivalents totaling $5.6 million and restricted cash totaling $4.8 thousand for a total of $5.6 million compared to $8.7 million at December 31, 2025. The following table sets forth the primary uses of cash for the nine months ended September 30, 2026 and 2025:


	2026		2025
Net Cash Used in Operating Activities	$	(5,610,785)	$	(7,780,721)
Net Cash (Used In) Provided by Investing Activities	$	(2,446,485)	$	9,077,523
Net Cash Provided by Financing Activities	$	4,910,592	$	265,359

Operating Activities. Net cash used in operating activities decreased $2.2 million primarily driven by a $2.7 million favorable change in working capital, partially offset by a $0.5 million increase in net loss adjusted for non-cash items. The favorable working capital change was primarily due to a smaller decrease in accrued expenses ($0.3 million in 2026 compared to $2.6 million in 2025), collections of collaboration receivables ($0.9 million inflow in 2026 compared to a $0.6 million outflow in 2025), and a decrease in tax and other receivables ($0.2 million inflow in 2026 compared to a $1.2 million outflow in 2025). These were partially offset by a $1.2 million unfavorable change in accounts payable (a $0.7 million decrease in 2026 compared to a $0.5 million increase in 2025) and the $1.25 million Senju option fee received in 2025, with no comparable receipt in 2026. Net loss increased $1.9 million, to $6.2 million from $4.3 million. Of that increase, $1.5 million was the non-cash change in fair value of contingent consideration: a $0.1 million charge in 2026 compared to a $1.3 million gain in 2025. Net cash used in operating activities for 2026 includes $835,000 received from CKD, which is the $1.0 million upfront payment net of Korean withholding tax.

Investing Activities. Net cash provided by investing activities decreased $11.5 million. The change was primarily driven by $7.3 million lower proceeds from maturities of marketable securities ($9.7 million in 2026 compared to $17.0 million in 2025), $3.9 million higher purchases of marketable securities ($12.1 million in 2026 compared to

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$8.2 million in 2025), and no sales of marketable securities in 2026 compared to $0.3 million in 2025, reflecting the investment of proceeds from the April 2026 private placement

Financing Activities. Net cash provided by financing activities increased by $4.6 million, rising from $0.3 million in the prior period to $4.9 million in the current period. This growth was heavily driven by $5.0 million in gross proceeds from the April 2026 private placement.

Funding Requirements and Other Liquidity Matters

Our product pipeline is still in various stages of preclinical and clinical development. We expect to continue to incur significant expenses and increasing operating losses for the foreseeable future. We anticipate that our expenses will increase substantially if and as we:

•seek marketing approval for our KIO-301 product outside of the territories already partnered with TOI and CKD;

•acquire or obtain license rights to any new products or product candidates;

•establish a sales and marketing infrastructure to commercialize our KIO-301 product outside of the territories already partnered with TOI and CKD or any other future development partner;

•add operational, financial and management information systems and personnel, including personnel to support our product development and future commercialization efforts;

•conduct the planned global Phase 3 clinical trial of KIO-401 in CRAO and Phase 2b clinical trial in NAION and make milestone payments to Senju under the KIO-401 License Agreement;

•seek marketing approval for our KIO-401 product or any other products that we successfully develop; and

•establish a sales and marketing infrastructure to commercialize our KIO-401 product or any other product candidate that we acquire, if approved.

Until such time, if ever, as we can generate substantial product revenue, we expect to finance our cash needs through a combination of equity offerings, debt financings, collaborations, strategic alliances, grants and licensing arrangements. We do not have any committed external source of funds. To the extent that we raise additional capital through the sale of equity or convertible debt securities, the ownership interest of our stockholders will be diluted, and the terms of these securities may include liquidation or other preferences that adversely affect the rights of holders of common stock. Debt financing, if available, may involve agreements that include covenants limiting or restricting our ability to take specific actions, such as incurring additional debt, making capital expenditures or declaring dividends. If we raise additional funds through collaborations, strategic alliances or licensing arrangements with pharmaceutical partners, we may have to relinquish valuable rights to our technologies, future revenue streams, research programs or product candidates, including our KIO-301 (outside of the territories already partnered with TOI and CKD), KIO-101, and KIO-104 products, on terms that may not be favorable to us. We have currently discontinued development work on KIO-104 and KIO-101, which are available for partnership for any further development of those programs. For our active programs, if we are unable to raise additional funds through equity or debt financings when needed, we may be required to delay, limit, reduce or terminate our product development or future commercialization efforts or grant rights to develop and market KIO-301 outside of the territories already partnered with TOI and CKD or any other future development partner and KIO-401 products, or any other products that we would otherwise prefer to develop and market ourselves.

Based on our cash on hand and short-term investments at September 30, 2026, we believe that we will have sufficient cash to fund planned operations into late 2027, excluding the technology transfer milestone, which may become payable prior to such date. However, the acceleration or reduction of cash outflows by management can significantly impact the timing for raising additional capital to complete development of our products. To continue development, we will need to raise additional capital through debt and/or equity financing, grants and other arrangements. Although historically we have been successful at raising capital, additional capital may not be available on terms favorable to us, if at all. We do not know if any future offerings will succeed. Accordingly, no assurances can be given that management will be successful in these endeavors. Our recurring losses from operations have caused management to determine there is substantial doubt about our ability to continue as a going concern. Our Condensed Consolidated Financial Statements do not include any adjustments to reflect the possible future effects on the recoverability and classification of assets or the amounts

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and classification of liabilities or any other adjustments that might be necessary should we be unable to continue as a going concern.

Other

For information regarding Commitments and Contingencies, refer to Note 9. Commitments and Contingencies to the Notes to the Condensed Consolidated Financial Statements of Part 1, Item 1. Financial Statements of this Form 10-Q.

Critical Accounting Estimates

Our discussion of operating results is based upon the Unaudited Condensed Consolidated Financial Statements and accompanying notes. The preparation of these statements requires us to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amount of revenues and expenses during the reporting period. Our critical accounting policies and significant judgement and estimates are detailed in Item 7 of our Annual Report on Form 10-K for the year ended December 31, 2025. During the quarter ended September 30, 2026, we applied our revenue recognition and collaboration policies to the CKD license agreement, which required judgments regarding the scope of ASC 808, the identification of performance obligations and the constraint on variable consideration. See Note 8 to the condensed consolidated financial statements. Other than as described above, as of September 30, 2026, we have no material changes from such disclosures.

Recently Issued Accounting Pronouncements

Information regarding new accounting pronouncements is included in Note 1 - Business, Presentation and Recent Accounting Pronouncements to the current period’s unaudited condensed consolidated financial statements.

Item 3. Quantitative and Qualitative Disclosures About Market Risk.

Not applicable.

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Item 4. Controls and Procedures.

This Report includes the certifications of our Chief Executive Officer (who is our principal executive officer) and our Chief Financial Officer (who is our principal financial and accounting officer) required by Rule 13a-14 of the Exchange Act. See Exhibits 31.1 and 31.2. This Item 4 includes information concerning the controls and control evaluations referred to in those certifications.

Evaluation of Disclosure Controls and Procedures

Disclosure controls and procedures (as defined in Rules 13a-15(e) and 15d-15(e) under the Exchange Act) are designed to ensure that information required to be disclosed in reports filed or submitted under the Exchange Act is recorded, processed, summarized, and reported within the time periods specified in SEC rules and forms and that such information is accumulated and communicated to management, including the Chief Executive Officer and Chief Financial Officer, to allow timely decisions regarding required disclosures.

In connection with the preparation of this Quarterly Report on the Form 10-Q, the Company’s Management, under the supervision of, and with the participation of, our Chief Executive Officer and Chief Financial Officer, conducted an evaluation of the effectiveness of the design and operation of our disclosure controls and procedures as of September 30, 2026. Our disclosure controls and procedures are designed to provide reasonable assurance that information required to be disclosed by us in the reports that we file or submit under the Exchange Act is recorded, processed, summarized and reported within the time periods specified in the SEC’s rules and forms, and our management necessarily was required to apply its judgment in evaluating and implementing our disclosure controls and procedures. Based upon the evaluation described above, our Chief Executive Officer and Chief Financial Officer have concluded that they believe that our disclosure controls and procedures were effective as of the end of the period covered by this report.

Changes in Internal Control over Financial Accounting and Reporting

There were no changes in the Company’s internal control over financial reporting during the three months ended September 30, 2026 that were identified in connection with management’s evaluation required by Rules 13a-15(d) and 15d-15(d) under the Exchange Act, that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.

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PART II - OTHER INFORMATION

Item 1. Legal Proceedings.

While we are not currently a party to any legal proceedings as of September 30, 2026, from time to time we may be a party to a variety of legal proceedings that arise in the normal course of our business.

Item 1A. Risk Factors.

In addition to the other information set forth in this report, you should carefully consider the risk factors discussed in Part I, “Item 1A. Risk Factors” in our Annual Report on Form 10-K for the year ended December 31, 2025, which is incorporated herein by reference and which could materially affect our business, financial condition or future results. The risks described herein and in that filing are not the only risks facing our Company. Additional risks and uncertainties not currently known to us or that we currently deem to be immaterial also may materially adversely affect our business, financial condition and/or operating results. Except as set forth below, there have been no material changes to the risk factors previously disclosed in our Annual Report on Form 10-K for the year ended December 31, 2025. The following risk factors supplement, and should be read together with, the risk factors described in our Annual Report.

We will be required to make significant milestone payments and will be subject to development and other obligations in connection with our license of KIO-401 from Senju.

Subsequent to the reporting period, we in-licensed KIO-401 from Senju and are subject to development, payment and other obligations, including the obligation to obtain regulatory approval in each country of our territory by January 1, 2040. If we fail to meet these obligations, Senju may terminate our rights in some or all of our territory, in which event we would not be able to develop, market or sell KIO-401. Termination of the Senju license agreement may result in us losing our rights under that agreement, including our rights to intellectual property and technology important to our development program. Any such termination would harm our business, financial condition and prospects significantly. We also rely on Senju to complete the transfer of manufacturing and clinical know-how and on Senju’s patent rights, which currently consist primarily of a pending formulation application.

Clinical data generated by Senju in Japan may not be accepted by the FDA or other regulators. We intend to rely in part on Phase 2 and Phase 3 data generated by Senju in Japan. Regulators may require additional trials, and the results of our planned global Phase 3 trial may not replicate prior results. Any additional trials would result in increased development costs for KIO-401, which would cause the value of our company to decline and limit our ability to obtain additional financing.

We will be required to make significant payments to Senju. We will pay Senju $3.5 million as an up-front payment, will make a $12.5 million payment upon completion of technology transfer, and may owe substantial regulatory, launch and sales milestones and royalties, which will require significant capital and may not be offset by product revenue. When obligations become due under the agreement, and if we are unable to raise sufficient capital in a timely manner, we may not have sufficient funds available to meet our obligations, which would adversely affect our business operations and financial condition. Moreover, even if we have sufficient funds, these obligations could materially reduce our ability to fund other programs.

Item 2. Unregistered Sales of Equity Securities and Use of Proceeds.

Unregistered Sales of Equity Securities

None.

Repurchase of Equity Securities

We did not repurchase any of our registered equity securities during the period covered by this Quarterly Report on Form 10-Q.

Net Share Settlement of Restricted Stock Awards

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The following table provides information with respect to shares of common stock withheld by the Company for net settlement of restricted stock awards during the three months ended September 30, 2026:


	Number of Shares9	Average Cost per Share		Total Number of Shares Purchased as Part of Publicly Announced Plans or Programs	Approximate Dollar Value of Shares that May Yet Be Purchased Under Plans or Programs
July 2026	2,780	$	2.66	—	—
August 2026	—	$	—	—	—
September 2026	—	$	—	—	—
Total	2,780	$	2.66	—	—

Item 3. Defaults Upon Senior Securities.

Not applicable.

Item 4. Mine Safety Disclosure.

Not applicable.

Item 5. Other Information.

No officers or directors, as defined in Rule 16a-1(f), adopted, modified or terminated a Rule 10b5-1 trading arrangement or a non-Rule 10b5-1 trading arrangement as defined in item 408 of Regulation S-K, during the three month period ended September 30, 2026.

Item 6. Exhibits

The exhibits filed as part of this Quarterly Report on Form 10-Q are set forth on the Exhibit Index immediately preceding such exhibits and are incorporated herein by reference.

9 Shares withheld to cover tax withholding obligations under net settlement provisions of restricted stock awards that vested during the period.

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SIGNATURES

Pursuant to the requirements of Section 13 and 15(d) of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.


Date: November 12, 2026	By:	/s/ Brian M. Strem, Ph.D.
		President and Chief Executive Officer (Principal executive officer)

Date: November 12, 2026	By:	/s/ Melissa Tosca
		Chief Financial Officer (Principal financial and accounting officer)

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EXHIBIT INDEX

The following exhibits are filed as part of this Quarterly Report on Form 10-Q. Where such filing is made by incorporation by reference to a previously filed document, such document is identified.


Exhibit Number						Description of Exhibit

10.1†						Exclusive License and Development Agreement, dated as of August 20 , 202 6 , by and between Kiora Pharmaceuticals, Inc. and Chong Kun Dang Pharmaceutical Corporation (incorporated by reference to Exhibit 10.1 to the Registrant's Current Report on Form 8-K filed with the SEC on August 19, 2026 ).

10.2#						Offer Letter by and between Kiora Pharmaceuticals, Inc. and Keith Lane dated as of June 22, 2026 (incorporated by reference to Exhibit 10.1 to the Registrant's Current R eport on Form 8-K filed with the SEC on September 8, 2026).

10.3† ††						Exclusive License Agreement by and between Kiora Pharmaceuticals, Inc. and Senju Pharmaceutical Co., Ltd., dated as of October 23, 2026 (incorporate d by reference to Exhibit 10.1 to the Registrant's Current Report on Form 8-K filed with the SEC on October 29, 2026).

31.1						Certification of principal executive officer pursuant to Rules 13a-15(e) and 15d-15(e), as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.

31.2						Certification of principal financial and accounting officer pursuant to Rules 13a-15(e) and 15d-15(e), as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.

32.1*						Certification of principal executive officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.

32.2*						Certification of principal financial and accounting officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.

101.INS						XBRL Instance Document (embedded within the Inline XBRL document)

101.SCH						XBRL Taxonomy Extension Schema Document

101.CAL						XBRL Taxonomy Extension Calculation Linkbase Document

101.DEF						XBRL Taxonomy Extension Definition Linkbase Document

101.LAB						XBRL Taxonomy Extension Labels Linkbase Document

101.PRE						XBRL Taxonomy Extension Presentation Linkbase Document

104						Cover Page Interactive Data File (embedded within the Inline XBRL document)

______________________________

* This certification shall not be deemed “filed” for purposes of Section 18 of the Exchange Act, or otherwise subject to the liability of that section, nor shall it be deemed to be incorporated by reference into any filing under the Securities Act.

† Schedules and exhibits have been omitted from this exhibit pursuant to Item 601(a)(5) of Regulation S-K. The registrant hereby undertakes to furnish copies of any of the omitted schedules and exhibits upon request by the U.S. Securities and Exchange Commission.

†† Certain confidential portions of this exhibit were omitted because the identified confidential portions (i) are not material and (ii) would be competitively harmful if publicly disclosed.

# Management contract or compensatory plan or arrangement.