Press Release: Inhibikase Therapeutics Announces Full Year 2025 Financial Results and Highlights Recent Activity

Dow Jones
Mar 27

WILMINGTON, Del., March 26, 2026 (GLOBE NEWSWIRE) -- Inhibikase Therapeutics, Inc. (Nasdaq: IKT) ("Inhibikase" or "Company"), a clinical-stage pharmaceutical company developing therapeutics to modify the course of cardiopulmonary diseases namely, Pulmonary Arterial Hypertension ("PAH"), today reported financial results for the year ended December 31, 2025 and highlighted recent developments.

"The fourth quarter of 2025 was a transformational quarter for the Company as we transitioned to a global pivotal Phase 3 clinical study in Pulmonary Arterial Hypertension following receipt of a Written Response from a Type C interaction from the United States Food and Drug Administration," said Mark Iwicki, Chief Executive Officer of Inhibikase. "With regulatory submissions in over 20 countries already filed and our first sites initiated, we are well-placed to advance enrollment in our global pivotal study, called IMPROVE-PAH, in PAH."

Recent Developments:

   -- The Company is advancing IKT-001 into a global pivotal Phase 3 study in 
      PAH: 
 
          -- The Phase 3 study, named IMPROVE-PAH (IKT-001 for Measuring 
             Pulmonary Vascular Resistance and Outcome Variables in a Phase 3 
             Evaluation of PAH; NCT07365332), has been initiated with 
             regulatory approval and the recent activation of our first 
             clinical sites in the United States. 
 
          -- Following receipt from the United States Food and Drug 
             Administration (the "FDA") of the Written Response from the 
             Company's Type C meeting interaction with the agency, the Company 
             is initiating a two-part adaptive Phase 3 study. 
 
                 -- Part A of IMPROVE-PAH is a double blind, placebo-controlled 
                    study in approximately 140 patients with a primary endpoint 
                    of Pulmonary Vascular Resistance ("PVR") at Week 24. 
 
                 -- Part B of IMPROVE-PAH, which shall immediately commence 
                    enrollment following enrollment of the last patient in Part 
                    A, adopts an identical format to Part A, except the primary 
                    endpoint will be 6-minute walk distance ("6MWD") at Week 24 
                    in approximately 346 patients. 
 
                 -- The Company believes this adaptive Phase 3 study design has 
                    important advantages including: (1) permitting a 12-week 
                    dose-titration phase designed to get patients to the 
                    highest tolerable dose of IKT-001; (2) uninterrupted 
                    enrollment between Part A and Part B; and (3) the ability 
                    to, if necessary, undertake a sample size re-estimation for 
                    Part B based on Part A findings. 
 
                 -- IMPROVE-PAH is expected to be conducted in up to 
                    approximately 180 sites around the world. 
 
          -- The Company is progressing regulatory approvals with submissions 
             in over 20 countries together with receiving confirmation of 
             acceptance under "Facilitating and Accelerating Strategic Trials 
             in the European Union", called FAST-EU, which is a pilot 
             initiative that commenced on January 30, 2026 to accelerate the 
             approval of multinational clinical trials. FAST-EU offers a 
             potential maximum 10-week (70-day) timeline for authorization, 
             integrating Ethics Committee opinions and improving efficiency 
             within the European Union Clinical Trials Information System. 
   -- Inhibikase successfully completed various required pre-clinical studies 
      that are necessary to support an application to the FDA for Orphan Drug 
      Designation for delivery of IKT-001 for PAH. Various information from 
      these studies is expected to be presented at the American Thoracic 
      Society International Conference to be held in Orlando, Florida on May 
      17th and 20th, 2026. 
 
   -- In November 2025, the Company completed a $115 million underwritten 
      public offering of its common stock and pre-funded warrants. 
 
          -- Aggregate gross proceeds from this offering were approximately 
             $115 million, before deducting underwriting discounts and 
             commissions and other offering expenses, excluding the exercise of 
             any pre-funded warrants. 

Financial Results

Cash Position: As of December 31, 2025, cash, cash equivalents and marketable securities were $178.8 million as compared to $97.5 million as of December 31, 2024.

Net Loss: Net loss for the year ended December 31, 2025, was $48.3 million, or $0.49 per share, compared to a net loss of $27.5 million, or $1.16 per share in the year ended December 31, 2024.

R&D Expenses: Research and development expenses were $29.8 million for the year ended December 31, 2025, which includes a non-cash write-off of in-process research and development of $7.4 million and $2.5 million of stock-based compensation expense, both associated with the Company's acquisition of CorHepta in February 2025, compared to $17.2 million for the year ended December 31, 2024.

SG&A Expenses: Selling, general and administrative expenses for the year ended December 31, 2025 were $23.6 million, which includes $1.0 million of severance expenses resulting from the transition of senior executives in the Company during the year, compared to $11.4 million for the year ended December 31, 2024.

About Inhibikase (www.inhibikase.com)

Inhibikase Therapeutics, Inc. (Nasdaq: IKT) is a clinical-stage pharmaceutical company developing therapeutics to modify the course of cardiopulmonary diseases, namely, Pulmonary Arterial Hypertension ("PAH"), in which aberrant signaling through type III receptor tyrosine kinases, including platelet derived growth factor receptors and a stem cell factor receptor, known as "c-Kit" has been implicated. Our lead product candidate is IKT-001, a prodrug of imatinib mesylate ("imatinib"), for PAH which is an orphan indication. Imatinib was first approved in the United States in 2001 for various cancers and blood disorders and, following more than 20 years of clinical use, has a well-characterized safety profile with the first reported use of imatinib in PAH occurring in 2005. PAH is a progressive, life-threatening disease characterized by pulmonary vascular remodeling and elevated pulmonary vascular resistance that affects approximately 50,000 Americans. Our single pivotal Phase 3 clinical study in PAH in approximately 180 sites around the world, named IMPROVE-PAH (IKT-001 for Measuring Pulmonary Vascular Resistance and Outcome Variables in a Phase 3 Evaluation of PAH), is actively enrolling patients.

Social Media Disclaimer

Investors and others should note that the Company announces material financial information to investors using its investor relations website, press releases, SEC filings and public conference calls and webcasts. The Company intends to also use LinkedIn and YouTube as a means of disclosing information about the Company, its services and other matters and for complying with its disclosure obligations under Regulation FD.

Forward-Looking Statements

This press release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking terminology such as "believes," "expects," "may," "will, " "should," "anticipates," "plans," or similar expressions or the negative of these terms and similar expressions are intended to identify forward-looking statements. These forward-looking statements include, but are not limited to, statements that express the Company's intentions, beliefs, expectations, strategies, predictions or any other statements related to the potential effects of IKT-001, the advancement of the Company's global pivotal Phase 3 clinical study of IKT-001 in PAH, including the timing, design, and conduct of the IMPROVE-PAH study and related regulatory submissions, the Company's beliefs regarding the potential advantages of the Phase 3 clinical study of IKT-001, or future events or conditions. These forward-looking statements are based on Inhibikase's current expectations and assumptions. Such statements are subject to certain risks and uncertainties, which could cause Inhibikase's actual results to differ materially from those anticipated by the forward-looking statements. Important factors that could cause actual results to differ materially from those in the forward-looking statements include our ability to commence and execute a Phase 3 study to evaluate IKT-001 as a treatment for PAH, as well as such other factors that are included in our periodic reports on Form 10-K and Form 10-Q that we file with the U.S. Securities and Exchange Commission. Any forward-looking statement in this release speaks only as of the date of this release. Inhibikase undertakes no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future developments or otherwise, except as may be required by any applicable securities laws.

Contacts:

Investor Relations:

Michael Moyer

LifeSci Advisors

mmoyer@lifesciadvisors.com

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