Kiora Pharmaceuticals swings to $1.75M Q3 2026 loss
At September 30, 2026, Kiora had approximately $16.3 million in cash and short-term investments and $2.2 million in receivables.
Sentiment and the balance of points
Rhea-AI Sentiment reads the wording of the document, how positive or negative its language is on a 1 to 5 scale. The balance of points shown with the takes weighs what the document actually discloses, so the two can disagree, for example when a trial that missed its main goal is described in upbeat language.
Form Type
8-K
Rhea-AI Filing Summary
Kiora Pharmaceuticals (KPRX) reported third-quarter 2026 results and clinical updates. It in-licensed exclusive development and commercialization rights outside Asia to KIO-401 (mitucapistat) from Senju Pharmaceutical, with Phase 2 and Phase 3 clinical data from Japan. Kiora submitted a Type B pre-IND meeting request and requested FDA orphan drug designation for KIO-401 in CRAO, and plans a registration trial in CRAO patients. KIO-301’s ABACUS-2 study is enrolling in the 100 mg cohort, with topline data expected by the end of 2027; Kiora licensed South Korean rights to CKD. It discontinued further R&D investment in KIO-104.
At September 30, 2026, cash and short-term investments were approximately $16.3 million, compared with $17.1 million at December 31, 2025; receivables were approximately $2.2 million. Third-quarter collaboration revenue from CKD was $1,000,000, with no comparable revenue recognized in Q3 2025. Net loss was $1,749,521, or $0.28 per basic and diluted share, versus net income of $26,806, or $0.01 per share. R&D expense was $1,949,864, compared with $2,729,891 a year earlier.
1 point · 0 major0 major · 1 point
How this balance works
Rhea-AI gives every point it takes from this document a weight. Minor counts 1, Moderate 3 and Major 9, so one Major point outweighs several Minor ones. The bar adds up the weights on each side, and when neither side holds more than 65% of the total the balance reads Mixed.
It reads the document as published, with the same rules for every company, and it does not look at what the market expected or at how the stock traded, so a point can be objectively good on a day the stock falls.
Rhea-AI Sentiment measures something else, the tone of the wording.
Positive
- Moderate pointKIO-301 collaboration revenue was $1,000,000 in Q3 2026, versus no comparable revenue in Q3 2025.
Negative
- Moderate pointThird-quarter net results shifted to a $1,749,521 loss from $26,806 income.
Filing Explained
Kiora’s September 30 balance sheet reports 4,424,387 common shares issued and outstanding, versus 3,761,739 at December 31, 2025; the higher outstanding-share base means a holder whose share count stayed constant would own a smaller fraction of the company.
8-K Event Classification
2 items: 2.02, 9.01
2 items
Item 2.02
Results of Operations and Financial Condition
Financial
Disclosure of earnings results, typically an earnings press release or preliminary financials.
Item 9.01
Financial Statements and Exhibits
Exhibits
Financial statements, pro forma financial information, or exhibit attachments filed with this report.
Key Figures
Cash and short-term investments: Approximately $16.3 million
Collaboration revenue: $1,000,000
Net loss: $1,749,521
+3 more
6 metrics
Cash and short-term investments
Approximately $16.3 million
At September 30, 2026; compared with $17.1 million at December 31, 2025
Collaboration revenue
$1,000,000
Three months ended September 30, 2026; no comparable revenue recognized in Q3 2025
Net loss
$1,749,521
Three months ended September 30, 2026; net income of $26,806 in Q3 2025
Net loss per basic and diluted share
$0.28 loss per share
Three months ended September 30, 2026; $0.01 income per share in Q3 2025
Research and development expenses
$1,949,864
Three months ended September 30, 2026, compared with $2,729,891 in Q3 2025
General and administrative expenses
$1,580,111
Three months ended September 30, 2026, compared with $1,443,827 in Q3 2025
Key Terms
calpain inhibitor, Type B pre-IND FDA meeting request, orphan drug designation, Central Retinal Artery Occlusion (CRAO), +1 more
5 terms
calpain inhibitor medical
"oral calpain inhibitor supported by Phase 2 and Phase 3 clinical data from Japan"
A calpain inhibitor is a drug or molecule that blocks the activity of calpains, a family of calcium-dependent cysteine proteases inside cells. By preventing calpains from cutting specific proteins, these inhibitors alter processes that calpains control—such as cytoskeleton remodeling, signal transduction and forms of programmed cell death—and are used in research and drug development to reduce calpain-driven tissue damage. Different calpain inhibitors vary in chemical structure and selectivity, so their effects and potential off-target protease interactions depend on the specific compound.
Type B pre-IND FDA meeting request regulatory
"Submitted a Type B pre-IND FDA meeting request and supporting materials"
orphan drug designation regulatory
"Submitted a request for FDA orphan drug designation for KIO-401 in CRAO"
Orphan drug designation is a special status given to medicines developed to treat rare diseases affecting only a small number of people. This status often provides benefits like faster approval processes and financial incentives, making it more attractive for companies to develop these drugs. For investors, it signals potential for exclusive market rights and reduced competition, which can impact the drug’s profitability.
Central Retinal Artery Occlusion (CRAO) medical
"patients who have experienced a Central Retinal Artery Occlusion (CRAO)"
collaboration credits financial
"After collaboration credits from Théa of $0.9 million and $1.7 million, respectively"
Earnings Snapshot
Collaboration revenue: $1,000,000
Third quarter ended September 30, 2026
Collaboration revenue
$1,000,000
No comparable revenue recognized in Q3 2025.
Net loss
$1,749,521
Net income of $26,806 in Q3 2025.
Net loss per basic and diluted share
$0.28 loss per share
$0.01 income per share in Q3 2025.
Research and development expenses
$1,949,864
Compared with $2,729,891 in Q3 2025.
General and administrative expenses
$1,580,111
Compared with $1,443,827 in Q3 2025.
FAQ
AI-generated questions and answers. How Rhea-AI works. Not financial advice.
What were Kiora Pharmaceuticals (KPRX)'s third-quarter 2026 results?
Kiora reported $1,000,000 in collaboration revenue and a $1,749,521 net loss for Q3 2026. Net loss was $0.28 per basic and diluted share, compared with net income of $26,806, or $0.01 per share, in Q3 2025. Research and development expenses were $1,949,864, compared with $2,729,891 a year earlier.
What is Kiora Pharmaceuticals (KPRX) planning for KIO-401 in CRAO?
Kiora plans a registration clinical trial in patients who have experienced CRAO and submitted a Type B pre-IND meeting request with supporting materials to discuss the IND pathway, trial design and approvable endpoints. It also requested FDA orphan drug designation; if granted, it would provide development incentives and eligibility for market exclusivity following approval.
AI-generated analysis. How Rhea-AI works. Not financial advice.
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, DC 20549
FORM 8-K
CURRENT REPORT PURSUANT
TO SECTION 13 OR 15(d) OF THE
SECURITIES EXCHANGE ACT OF 1934
Date of report (Date of earliest event reported): November 12, 2026
(Exact name of registrant as specified in its charter)
(State or other jurisdiction of incorporation)
| (Commission File Number) | (IRS Employer Identification No.) | ||||
(858 ) 224-9600
(Registrant’s telephone number, including area code)
(Former name or former address, if changed since last report)
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) | |||||
| Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) | |||||
| Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) | |||||
| Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) | |||||
Securities registered pursuant to Section 12(b) of the Act:
| Title of each class: | Trading Symbol(s) | Name of each exchange on which registered: | ||||||||||||
Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
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. ☐
Item 2.02. Results of Operations and Financial Conditions.
On November 12, 2026, Kiora Pharmaceuticals, Inc. (the “Company”) issued a press release announcing financial results for the quarter ended September 30, 2026 and an update on clinical development progress. A copy of the release is attached as Exhibit 99.1.
The information furnished pursuant to this Item 2.02, including Exhibit 99.1, is not deemed to be “filed” for purposes of Section 18 of the Exchange Act, or otherwise subject to the liability of that section. This information will not be deemed to be incorporated by reference into any filing under the Securities Act or the Exchange Act, except to the extent that the registrant specifically incorporates them by reference.
Item 9.01. Financial Statements and Exhibits.
(d) Exhibits.
| Exhibit Number | Title | |||||||
99.1 | Press Release of Kiora Pharmaceuticals, Inc., dated as of November 12, 2026 | |||||||
| 104 | Cover Page Interactive Data File (embedded within the Inline XBRL document). | |||||||
*Schedules and exhibits have been omitted 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.
SIGNATURES
Pursuant to the requirements 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.
| KIORA PHARMACEUTICALS, INC. | ||||||||
| By: | /s/ Melissa Tosca | |||||||
| Melissa Tosca | ||||||||
| Chief Financial Officer | ||||||||
| (Principal financial and accounting officer) | ||||||||
| Date: | November 12, 2026 | |||||||
Exhibit 99.1
Kiora Pharmaceuticals Reports Third Quarter 2026 Financial Results and Provides Corporate Update
SAN DIEGO, California — November 12, 2026 — Kiora Pharmaceuticals, Inc. (NASDAQ: KPRX) (“Kiora” or the “Company”) today reported financial results for the third quarter ended September 30, 2026, and provided a business update highlighted by the in-licensing of KIO-401, a late-stage, oral neuroprotective calpain inhibitor. The addition transforms Kiora’s development pipeline, bringing an asset supported by existing Phase 2 and Phase 3 studies conducted in Japan. Kiora is planning a multinational registration clinical trial in patients who have experienced a Central Retinal Artery Occlusion (CRAO).
Third Quarter 2026 and Recent Highlights
•Acquired late-stage lead asset: In-licensed exclusive development and commercialization rights, outside of Asia, to KIO-401 (mitucapistat) from Senju Pharmaceutical Co., Ltd., an oral calpain inhibitor supported by Phase 2 and Phase 3 clinical data from Japan.
•KIO-401 FDA engagement underway: Submitted a Type B pre-IND FDA meeting request and supporting materials to begin discussions regarding the investigational new drug application (IND) pathway, trial design and approvable endpoints for KIO-401.
•KIO-401 orphan drug designation requested: Submitted a request for FDA orphan drug designation for KIO-401 in CRAO. If granted, designation would provide development incentives and eligibility for market exclusivity following approval.
•KIO-301 ABACUS-2 trial is progressing: The clinical trial is actively enrolling and dosing patients in the 100 mg dose cohort.
•KIO-301 development and commercial network expanded: Out-licensed development and commercial rights for KIO-301 in South Korea to Chong Kun Dang Pharmaceutical Corporation (CKD).
•Expanded leadership team: Appointed Keith Lane, MBA, former Chief Scientific Officer of Ora, Inc., as EVP of Clinical Development and Regulatory Affairs. Mr. Lane has overseen more than 100 clinical trials, including more than 10 global, pivotal Phase 3 ophthalmic studies.
•Cash position: Ended the quarter with approximately $16.3 million in cash and short-term investments plus $2.2 million in collaboration, tax and other receivables.
KIO-401: Transforming Kiora’s Development Pipeline
“The addition of KIO-401 transforms Kiora into a late-stage retinal therapeutics company,” said Brian M. Strem, Ph.D., President and Chief Executive Officer of Kiora. “We are building on the significant amount of CMC, non-clinical and clinical data that already exists on KIO-401 through Senju’s previous and ongoing efforts. With exclusive rights outside Asia, we are preparing for a single, phase 3, registration trial of KIO-401 in patients across the United States, Europe and other territories. We believe an effective oral therapy that restores greater amounts of vision following an acute ischemic event could offer meaningful patient benefit and significant commercial value. Our strategy is to establish KIO-401 in CRAO and build on that foundation through additional ophthalmic indications, such as non-arteritic anterior ischemic optic neuropathy (NAION).
“Calpains are calcium-activated enzymes which, when dissociated from the endogenous inhibitor, are understood to initiate and regulate programmed cell death via the breakdown of multiple proteins essential to cell function and survival. KIO-401 inhibits this adverse activity, keeping cells alive and buying time for the body to restore homeostasis. Beyond KIO-401, we see opportunities for next-generation products and could cost-effectively evaluate one or more preclinical candidates in indications ranging from chronic ophthalmic diseases to neurodegenerative conditions or cardiovascular diseases.”
Patients with CRAO and NAION often experience sudden, permanent vision loss. Neither condition has an approved pharmacologic treatment nor any intervention that has demonstrated meaningful success in returning vision after these acute events. In Japan, the Phase 2a study reported a statistically significant visual-acuity improvement compared with a prospective observational registry (p=0.0398). The subsequent randomized, double-masked Phase 3 study showed a numerical improvement in the overall visual-acuity comparison (p=0.0949), with a statistically significant improvement among patients who were legally blind (as defined by the World Health Organization) at baseline (p=0.0195). These findings inform Kiora’s planned design of a larger trial to evaluate clinical benefit.
“The separation between KIO-401 and placebo and the continued trajectory in visual acuity in the active-treatment group through the final 12-week assessment provide further encouragement that a sufficiently powered registration study could support approval in the United States, Europe and other regions,” said Keith J. Lane, MBA, Executive Vice President of Clinical Development and Regulatory Affairs of Kiora. “To gain clarity as
soon as possible, we’ve already submitted the meeting request and supporting materials to begin dialogue with the FDA regarding the IND pathway, trial design and endpoints for our planned CRAO registration trial. Further, we submitted a request to the FDA in early November for orphan drug designation for KIO-401 in CRAO. If granted, it would provide development incentives and eligibility for market exclusivity in the respective markets following approval.”
KIO-301 and Portfolio Priorities
KIO-301 remains in Phase 2 development for patients living with vision loss due to advanced retinitis pigmentosa. ABACUS-2 is enrolling patients in the 100 mg cohort with strong patient demand to participate in the trial. Kiora remains on track for topline data by the end of 2027, while its collaboration with Théa Open Innovation provides reimbursement of all associated research and development expenses. The Company also expanded KIO-301’s regional partnerships during the quarter through a license of South Korean rights to CKD. Should the asset be advanced further, Kiora is eligible for potential development milestone payments, additional regulatory milestones and royalties.
As announced in October 2026, Kiora discontinued further research and development investment in KIO-104. The Company plans to report results from patients enrolled in the KLARITY study and evaluate partnering opportunities.
Third Quarter 2026 Financial Results
“Our current cash position enables us to fund pre-trial activities needed to prepare KIO-401 for its next stage of development, including CMC and regulatory work ahead of enrollment and dosing, when spending will increase,” said Melissa Tosca, CPA, Chief Financial Officer of Kiora. “Reimbursement of KIO-301-related research and development expenses and our decision to discontinue KIO-104 support this financial flexibility. We will continue to maintain a streamlined operation, aligning spending with development milestones. Our resources also allow us to fund initial preclinical evaluation of next-generation calpain inhibitors in ophthalmic and non-ophthalmic indications. This disciplined approach enables us to advance these activities and seek greater clarity on Phase 3 trial requirements.”
Kiora ended the third quarter with approximately $16.3 million in cash and short-term investments, compared with $17.1 million as of December 31, 2025. The Company recorded $0.6 million in collaboration receivables and $1.6 million in tax and other receivables as of September 30, 2026.
Collaboration revenue was $1.0 million for the third quarter of 2026 related to the KIO-301 development and commercialization agreement with CKD. There was no comparable revenue recognized in the third quarter of 2025.
Research and development expenses were approximately $1.9 million for the third quarter of 2026, compared with $2.7 million for the third quarter of 2025. After collaboration credits from Théa of $0.9 million and $1.7 million, respectively, net research and development expenses were approximately $1.0 million and $1.1 million. The change primarily reflected lower preclinical and manufacturing costs for KIO-301 following completion of activities that supported the ABACUS-2 Phase 2 trial, which drove a corresponding decrease in reimbursable expenses from Théa, as well as lower personnel-related costs.
General and administrative expenses were approximately $1.6 million, compared with $1.4 million in the prior-year quarter, reflecting higher professional services costs, primarily legal fees related to our expanded patent portfolio and general corporate matters, as well as increased investor relations and consulting costs. These increases were partially offset by lower personnel-related costs.
Net loss for the third quarter of 2026 was approximately $1.7 million, or $0.28 per basic and diluted share, compared with net income of approximately $27,000, or $0.01 per basic and diluted share, for the third quarter of 2025.
About Kiora Pharmaceuticals
Kiora Pharmaceuticals develops small-molecule treatments for vision-threatening retinal diseases. Its pipeline includes KIO-401, an investigational, oral neuroprotective therapy for acute ischemic ophthalmic conditions, and KIO-301, a partnered molecular photoswitch being evaluated for advanced retinitis pigmentosa.
For more information, visit www.kiorapharma.com.
Forward-Looking Statements
Some of the statements in this press release are “forward-looking” statements made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. These statements include, without limitation, statements concerning Kiora’s planned development and potential commercialization of KIO-401; the anticipated timing, design, initiation, conduct, enrollment, dosing, endpoints, follow-up periods and results of clinical trials in CRAO and NAION; the potential to incorporate additional patient follow-up without extending overall trial timelines; the potential efficacy, safety, therapeutic benefit and commercial opportunity of KIO-401; the interpretation and applicability of clinical results generated by Senju Pharmaceutical in Japan; anticipated regulatory interactions, feedback and approvals, including discussions regarding the IND pathway and registration requirements in the United States and Europe; requests for orphan drug designation and the potential availability of related development incentives and market exclusivity; the potential development and preclinical evaluation of next-generation calpain inhibitors in ophthalmic and non-ophthalmic indications; the ability to leverage existing clinical development infrastructure and maintain streamlined operations; the expected progression of the KIO-301 program and reimbursement of associated research and development expenses; the Company’s plans for KIO-104; the sufficiency of the Company’s existing cash and investments to fund pre-trial activities and initial preclinical evaluations; and the expected capital requirements associated with its development programs.
These forward-looking statements are based on management’s current expectations and assumptions and involve risks and uncertainties that could cause actual results to differ materially from those expressed or implied. Such risks include, among others, uncertainties associated with preclinical and clinical development and regulatory review; the possibility that results observed in previous studies will not be reproduced in future studies; the possibility that regulatory feedback will require changes to proposed trial designs, endpoints, follow-up periods or development timelines; the possibility that orphan drug designation will not be granted or that anticipated incentives or exclusivity will not be available; the cost, timing, enrollment, conduct and outcomes of clinical trials; the Company’s ability to maintain anticipated collaboration reimbursements and manage operating expenses; the ability to obtain sufficient capital to fund planned development activities; the availability and terms of future financings; potential dilution to existing stockholders; the Company’s ability to execute its development strategy and licensing obligations; and other risks described under “Risk Factors” in Kiora’s Annual Report on Form 10-K filed with the SEC on March 25, 2026, and in its subsequent filings with the SEC.
Kiora’s results may also be affected by factors of which the Company is not currently aware. Forward-looking statements speak only as of the date of this release. Except as required by law, Kiora undertakes no obligation to publicly update or revise any forward-looking statement to reflect subsequent events, circumstances or changes in expectations.
Contacts: Investors
Investors@kiorapharma.com
Financial Tables Follow
Financial Tables Follow
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 | |||||||
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 | $ | (1,739,331) | $ | 28,867 | $ | (6,245,985) | $ | (4,280,183) | |||||||||||||||