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Inhibikase Therapeutics Announces 2024 Financial Results and Highlights Recent Activity

1. Inhibikase focuses on advancing IkT-001 for pulmonary arterial hypertension. 2. Company raised $110 million for late-stage clinical trials of IkT-001. 3. Mark Iwicki leads a newly strengthened management team in PAH treatments. 4. IkT-001's active ingredient shows promise as a disease-modifying therapy. 5. 2024's net loss was $27.5 million, but cash reserves improved significantly.

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Why Bullish?

The focus on IkT-001's late-stage trials increases investor confidence, similar to other biotech advancements that drove stock prices higher in comparable situations.

How important is it?

The positioning for clinical trials and management changes are pivotal for IKT’s future profitability and stock valuation.

Why Long Term?

The progression of clinical trials often leads to sustainable growth in share prices over the long term, akin to previous pharmaceutical breakthroughs like Amgen's successful trials.

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New Leadership and Focus on Advancement of IkT-001 into a Late-Stage Clinical Trial Program in Pulmonary Arterial Hypertension March 27, 2025 16:01 ET  | Source: Inhibikase Therapeutics BOSTON, March 27, 2025 (GLOBE NEWSWIRE) -- Inhibikase Therapeutics, Inc. (Nasdaq: IKT) (“Inhibikase” or “Company”), a clinical-stage pharmaceutical company innovating small molecule kinase inhibitor therapeutics to treat pulmonary arterial hypertension (“PAH”), today reported financial results for the year ended December 31, 2024 and highlighted recent developments. “The financing concluded in October positioned us to focus our clinical development efforts on advancing IkT-001 toward a late-stage clinical trial in PAH,” said Mark Iwicki, Chief Executive Officer of Inhibikase. “To drive the Company toward its next phase of growth, we subsequently added depth to our management team with the additions of Chris Cabell and John Adams, two accomplished scientific leaders with established track records in the PAH space. Additionally, we expect Chris and John will enable us to accelerate the build out of our team as we make preparations to execute on the IkT-001 Phase 2b clinical trial in PAH. We enter 2025 well positioned to aggressively advanced our IkT-001 development plan.” Recent Developments: Closed a private placement with gross proceeds of approximately $110 million in October 2024 in support of advancing IkT-001 into a late-stage clinical trial in PAH. If the warrants issued in such offering are exercised for cash, the aggregate total gross proceeds from the financing may be up to $275 million.Announced the appointments of Mark Iwicki as Chief Executive Officer, Chris Cabell, M.D., MHS, FACC, as President and Head of Research & Development, and John Adams, Ph.D., as Chief Scientific Officer.Added highly accomplished leaders in biopharmaceutical development to the Board of Directors of the Company (the “Board”): Amit Munshi, Chief Executive Officer of Orna Therapeutics and former CEO of Arena Pharmaceuticals; Mr. Munshi has been appointed as the independent Chair of the Board.Vince Aurentz, former Executive Vice President and Chief Business Officer at Arena Pharmaceuticals and former member of the Board at Longboard Pharmaceuticals, Inc.Roberto Bellini, Managing Partner of BSQUARED Capital and former Chief Executive Officer of BELLUS Health Inc.David Canner, Partner at Soleus Capital.Mark Iwicki, Chair of the Board of Akero Therapeutics.Arvind Kush, Chief Financial Officer and Chief Business Officer of Candid Therapeutics and former CFO of RayzeBio. Advancement of IkT-001 as a therapy in Pulmonary Arterial Hypertension: The Company received its Study May Proceed letter for the Phase 2b trial in September 2024.The active ingredient in IkT-001, imatinib, has previously been shown to be disease-modifying for PAH. 2024 Financial Results Net Loss: Net loss for the year ended December 31, 2024, was $27.5 million, or $1.16 per share, compared to a net loss of $19.1 million, or $3.16 per share in the year ended December 31, 2023. R&D Expenses: Research and development expenses were $17.2 million for the year ended December 31, 2024 compared to $13.6 million in the year ended December 31, 2023. SG&A Expenses: Selling, general and administrative expenses for the year ended December 31, 2024 were $11.4 million compared to $6.7 million for the year ended December 31, 2023. Cash Position: Cash, cash equivalents and marketable securities were $97.5 million as of December 31, 2024. Grant of Inducement Awards Under Nasdaq Listing Rule 5635(c)(4) The Board approved the grant of non-statutory stock options to each of Mr. Adams and Mr. Cabell to purchase an aggregate of 2,250,000 and 2,810,000 shares of common stock, respectively, as an inducement material to the employees’ acceptance of employment with the Company in accordance with Nasdaq Listing Rule 5635(c)(4). The options have an exercise price of $2.97 per share, which is equal to the closing price of the Company’s common stock on February 21, 2025, the effective date of grant. The options have a ten year term, vesting annually over three years, commencing on the one-year anniversary of the employee’s date of hire. The options are subject to the employee’s continued service with the Company on each such vesting date and the terms and conditions of an award agreement. About Inhibikase (www.inhibikase.com) Inhibikase Therapeutics, Inc. (Nasdaq: IKT) is a clinical-stage pharmaceutical company developing Abelson Tyrosine Kinase inhibitor therapeutics for Cardiopulmonary disease. Inhibikase’s cardiopulmonary disease portfolio is led by IkT-001, a prodrug of imatinib mesylate, for PAH. Inhibikase is headquartered in Atlanta, Georgia with offices in Lexington, Massachusetts. 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 X, Facebook, 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 initiation of the Company’s Phase 2b trial of IkT-001 in PAH, the Company’s future activities, or future events or conditions; and expectations regarding the anticipated contribution of Dr. Cabell and Dr. Adams to our operations and progress. 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 2b ‘702’ trial 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 MoyerLifeSci Advisorsmmoyer@lifesciadvisors.com ---tables to follow---  Inhibikase Therapeutics, Inc.Consolidated Balance Sheets(Unaudited)         December 31,2024  December 31,2023        Assets    ​ Current assets:    ​ Cash and cash equivalents $56,490,579  $9,165,179 Marketable securities  41,052,949   4,086,873 Prepaid research and development  81,308   219,817 Prepaid expenses and other current assets  826,473   739,179 Total current assets  98,451,309   14,211,048 Equipment and improvements, net  47,100   73,372 Right-of-use asset  101,437   222,227 Total assets $98,599,846  $14,506,647 Liabilities and stockholders’ equity    ​ Current liabilities:    ​ Accounts payable $943,019  $646,767 Lease obligation, current  110,517   150,095 Accrued expenses and other current liabilities  2,680,030   2,259,955 Insurance premium financing payable  -   381,784 Total current liabilities  3,733,566   3,438,601 Lease obligation, net of current portion  -   90,124 Total liabilities  3,733,566   3,528,725 Commitments and contingencies    ​ Stockholders’ equity: ​  ​ Preferred stock, $0.001 par value; 10,000,000 shares authorized; 0 shares issued and outstanding at December 31, 2024 and December 31, 2023  -   - Common stock, $0.001 par value; 100,000,000 shares authorized; 69,362,439 and 6,186,280 shares issued and outstanding at December 31, 2024 and December 31, 2023  69,362   6,186 Additional paid-in capital  189,254,777   77,871,584 Accumulated other comprehensive (loss) income  (37,248)  877 Accumulated deficit  (94,420,611)  (66,900,725)Total stockholders' equity  94,866,280   10,977,922 Total liabilities and stockholders’ equity $98,599,846  $14,506,647          Inhibikase Therapeutics, Inc.Condensed Consolidated Statements of Operations and Comprehensive Loss(Unaudited)      Year ended December 31,   2024  2023 Revenue:      Grant revenue $—  $260,501 Total revenue  —   260,501 Costs and expenses:      Research and development  17,210,548   13,618,348 Selling, general and administrative  11,378,520   6,731,945 Total costs and expenses  28,589,068   20,350,293 Loss from operations  (28,589,068)  (20,089,792)Interest income  1,069,182   1,060,909 Net loss  (27,519,886)  (19,028,883)Other comprehensive loss, net of tax      Unrealized loss on marketable securities  (38,125)  (103,841)Comprehensive loss $(27,558,011) $(19,132,724)Net loss per share – basic and diluted $(1.16) $(3.16)Weighted-average number of common shares – basic and diluted  23,712,220   6,028,210          

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