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Inhibikase Therapeutics Announces Second Quarter 2025 Financial Results and Highlights Recent Activity

1. IKT is advancing IKT-001 for Pulmonary Arterial Hypertension. 2. Phase 2b trial of IKT-001 to start in the second half of 2025. 3. Net loss increased significantly compared to last year. 4. Cash position at $87.7 million as of June 30, 2025. 5. R&D expenses rose due to acquisition-related costs.

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Why Bullish?

The initiation of the Phase 2b trial offers potential for positive outcomes, similar to past successes with imatinib. Successful trials could enhance market confidence and lead to price appreciation, evidenced by historical examples where trial announcements led to increased stock prices in biotech companies.

How important is it?

The results and progress with IKT-001 are pivotal in determining IKT's future valuation, thus warranting a high importance score. The increase in R&D expenses also indicates active development, increasing investor interest.

Why Short Term?

The impending Phase 2b trial initiation is expected to influence short-term investor sentiment, similar to past industry examples where trial news accelerated stock movements. Market reactions are typically immediate surrounding these trial initiations.

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IMPNAXGTCLGN
August 14, 2025 16:50 ET  | Source: Inhibikase Therapeutics BOSTON and ATLANTA, Aug. 14, 2025 (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 quarter ended June 30, 2025 and highlighted recent developments. “During our second quarter of 2025, we continued to position the Company to advance IKT-001 toward a late-stage clinical trial in PAH,” said Mark Iwicki, Chief Executive Officer of Inhibikase. “We have now finalized our study protocol, and we expect to initiate our Phase 2b clinical study of IKT-001, our re-engineered prodrug of imatinib mesylate, in PAH in the second half of 2025.” Multiple studies including both Phase 2 and the Phase 3 IMPRES study previously demonstrated that imatinib mesylate (“imatinib”), an anti-proliferative tyrosine kinase inhibitor, was highly efficacious in PAH. Notably in the IMPRES study, patients that maintained 400 mg of imatinib for greater than 50% of the treatment period showed a placebo adjusted 45-meter improvement in 6-minute walk distance (“6MWD”) which represents best-in-class improvements for patients afflicted by PAH. More recently, a contemporary study in the American Journal of Respiratory and Critical Care Medicine demonstrated that higher exposures of imatinib were associated with a larger improvement in total pulmonary resistance (“TPR”). The 400 mg dose of imatinib exhibited the greatest impact on TPR and, even though the majority of patients completed the study at 200 mg or less, the magnitude of the hemodynamic change for the study was noted to compare favorably with recent studies of novel therapies added to background treatment. The Company believes this supports its thesis that IKT-001 has the potential to minimize GI side effects while maximizing the highly efficacious outcomes observed at 400 mg across multiple studies. Recent Developments: Advancement of IKT-001 as a therapy in PAH: During the first half of 2025, the Company evaluated potential study designs and obtained feedback from various key opinion leaders before finalizing a clinical study protocol for its forthcoming Phase 2b study, known as IMPROVE-PAH.IMPROVE-PAH is a multi-center, randomized, double-blind, placebo-controlled study of approximately 150 PAH participants. Participants under IMPROVE-PAH will be randomized 1:1:1 to receive 300 mg IKT-001, 500 mg IKT-001, or placebo once daily for 26 weeks, in addition to stable background PAH therapy. The Company’s bioequivalence studies previously confirmed that 500 mg of IKT-001 has comparable exposure in humans to 380 mg of imatinib. The primary efficacy endpoint is change in pulmonary vascular resistance at Week 26. Secondary endpoints include 6MWD, World Health Organization functional class, and pharmacokinetics. The study protocol also includes an interim safety review for study continuance by the Data Safety Monitoring Board with at least 50 patients at 12-weeks of follow-up.The Company expects to initiate IMPROVE-PAH in the second half of 2025. Financial Results Cash Position: As of June 30, 2025, cash, cash equivalents and marketable securities were $87.7 million as compared to $97.5 million as of December 31, 2024. Net Loss: Net loss for the quarter ended June 30, 2025, was $9.9 million, or $0.11 per share, compared to a net loss of $5.0 million, or $0.66 per share in the quarter ended June 30, 2024. Net loss for the six months ended June 30, 2025, was $23.6 million, or $0.26 per share, compared to a net loss of $9.6 million, or $1.38 per share, for the six months ended June 30, 2024. R&D Expenses: Research and development expenses were $5.3 million for the quarter ended June 30, 2025, compared to $3.1 million for the quarter ended June 30, 2024. Research and development expenses were $15.8 million for the six months ended June 30, 2025, which includes a non-cash write-off of in-process research and development of $7.4 million and $1.0 million of stock-based compensation expense, both associated with the Company’s acquisition of CorHepta in February 2025, compared to $5.8 million for the six months ended June 30, 2024. SG&A Expenses: Selling, general and administrative expenses for the quarter ended June 30, 2025 were $5.9 million, compared to $2.0 million for the quarter ended June 30, 2024. Selling, general and administrative expenses for the six months ended June 30, 2025 were $11.2 million, which includes $1.0 million of severance expenses resulting from the transition of senior executives in the Company during the year, compared to $4.0 million for the six months ended June 30, 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, PAH, that arise from aberrant signaling through the Abelson Tyrosine Kinase, and type III receptor tyrosine kinases including platelet derived growth factor receptors and c-KIT. Our lead product candidate is IKT-001, a prodrug of imatinib mesylate, for PAH which is an orphan indication. PAH is a progressive, life-threatening disease characterized by pulmonary vascular remodeling and elevated pulmonary vascular resistance that affects approximately 50,000 Americans. 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 initiation of the Company’s Phase 2b trial of IKT-001 in PAH and the Company’s future activities, 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 2b 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. Condensed Consolidated Balance Sheets (Unaudited)         June 30,2025  December 31,2024   (unaudited)  (Note 3) Assets    ​ Current assets:    ​ Cash and cash equivalents $77,742,669  $56,490,579 Marketable securities  9,923,100   41,052,949 Prepaid research and development  138,855   81,308 Deferred offering costs  307,373   — Prepaid expenses and other current assets  682,628   826,473 Total current assets  88,794,625   98,451,309 Equipment and improvements, net  23,687   47,100 Right-of-use asset  34,918   101,437 Total assets $88,853,230  $98,599,846 Liabilities and stockholders’ equity    ​ Current liabilities:    ​ Accounts payable $2,703,554  $943,019 Lease obligation, current  37,944   110,517 Accrued expenses and other current liabilities  3,145,888   2,680,030 Contingent consideration liability  2,912,159   — Total current liabilities  8,799,545   3,733,566 Total liabilities  8,799,545   3,733,566 Commitments and contingencies (see Note 16)    ​ Stockholders’ equity: ​  ​ Preferred stock, $0.001 par value; 10,000,000 shares authorized; 0 shares issued and outstanding at June 30, 2025 and December 31, 2024  —   — Common stock, $0.001 par value; 500,000,000 and 100,000,000 shares authorized; 74,516,635 and 69,362,439 shares issued and outstanding (including 4,149,252 and 0 contingently issuable shares - see Note 10) at June 30, 2025 and December 31, 2024, respectively  74,516   69,362 Additional paid-in capital  197,996,982   189,254,777 Accumulated other comprehensive loss  (2,944)  (37,248)Accumulated deficit  (118,014,869)  (94,420,611)Total stockholders' equity  80,053,685   94,866,280 Total liabilities and stockholders’ equity $88,853,230  $98,599,846         Inhibikase Therapeutics, Inc.Condensed Consolidated Statements of Operations and Comprehensive Loss(Unaudited)         Three Months Ended June 30,  Six months ended June 30,   2025  2024  2025  2024 Costs and expenses:            Research and development $5,270,967  $3,075,830  $15,784,546  $5,827,109 Selling, general and administrative  5,919,731   1,974,705   11,169,022   4,005,786 Change in fair value contingent consideration  (358,420)  —   (1,523,284)  — Total costs and expenses  10,832,278   5,050,535   25,430,284   9,832,895 Loss from operations  (10,832,278)  (5,050,535)  (25,430,284)  (9,832,895)Interest income  916,755   90,927   1,836,026   223,652 Net loss  (9,915,523)  (4,959,608)  (23,594,258)  (9,609,243)Other comprehensive income (loss), net of tax            Unrealized gain (loss) on marketable securities  (1,977)  776   34,304   (1,901)Comprehensive loss $(9,917,500) $(4,958,832) $(23,559,954) $(9,611,144)Net loss per share – basic and diluted $(0.11) $(0.66) $(0.26) $(1.38)Weighted-average number of shares – basic and diluted  90,009,625   7,535,667   89,774,703   6,939,779                   Inhibikase Therapeutics, Inc.Condensed Consolidated Statements of Cash Flows(Unaudited)      Six months ended June 30,   2025  2024 Cash flows from operating activities      Net loss $(23,594,258) $(9,609,243)Adjustments to reconcile net loss to net cash used in operating activities:      Depreciation  36,812   13,137 Stock-based compensation expense  6,250,938   84,131 Write-off of in-process research and development  7,357,294   — Change in fair value of contingent consideration  (1,523,284)  — Changes in operating assets and liabilities:      Operating lease right-of-use assets  66,519   58,465 Prepaid expenses and other assets  7,526   30,719 Prepaid research and development  (57,547)  (86,483)Accounts payable  1,592,656   875,701 Operating lease liabilities  (72,573)  (62,389)Accrued expenses and other current liabilities  258,156   (225,430)Net cash used in operating activities  (9,677,761)  (8,921,392)       Cash flows from investing activities      Purchases of equipment and improvements  (13,399)  — Purchases of investments - marketable securities  —   (9,209,545)Maturities of investments - marketable securities  31,350,103   8,440,958 Acquired in-process research and development  (438,624)  — Net cash provided by (used in) investing activities  30,898,080   (768,587)       Cash flows from financing activities      Proceeds from issuance of common stock, pre-funded warrants and warrants, net of issuance costs  150   3,611,255 Issuance of common stock form exercise of stock options  31,621   — Net cash provided by financing activities  31,771   3,611,255 Net increase (decrease) in cash and cash equivalents  21,252,090   (6,078,724)Cash and cash equivalents at beginning of period  56,490,579   9,165,179 Cash and cash equivalents at end of period $77,742,669  $3,086,455 Supplemental disclosures of cash flow information      Issuance costs $—  $1,203,350 Non cash investing and financing activities      Non-cash financing costs $—  $(181,930)CorHepta transaction costs $175,000  $— Contingent consideration $2,912,159  $— Deferred offering costs included in accounts payable and accrued expenses $307,373  $— 

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