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Inhibikase Therapeutics Secures $275M Financing, Advances IkT-001Pro for Pulmonary Arterial Hypertension

Inhibikase Therapeutics has secured up to $275 million in financing from healthcare-focused investors, led by Soleus Capital. The company is advancing IkT-001Pro, an optimized prodrug of imatinib, into late-stage clinical trials as a potential first oral disease-modifying treatment for pulmonary arterial hypertension. The FDA has designated IkT-001Pro as a New Molecular Entity, making it eligible for exclusivity designations.

Inhibikase Therapeutics (Nasdaq: IKT) has secured a transformative financing package worth up to $275 million from top-tier healthcare investors, marking a significant advancement in their development of novel treatments for pulmonary arterial hypertension (PAH).
The financing round, led by Soleus Capital, includes an initial $110 million private placement, positioning the company to accelerate the development of IkT-001Pro, an optimized prodrug of imatinib designed as a potential first-in-class oral treatment for PAH.

Strategic Focus on Pulmonary Arterial Hypertension

PAH represents a critical unmet medical need, primarily affecting women between ages 30 and 60. The condition is characterized by progressive narrowing of pulmonary arteries, leading to increased blood pressure in the lungs and eventual right heart failure if left untreated.
IkT-001Pro has received significant regulatory support, with the FDA designating it as a New Molecular Entity (NME) during recent pre-IND meeting discussions. This designation opens the pathway for various exclusivity opportunities in the PAH indication.

Development Strategy and Clinical Pathway

The company plans to advance IkT-001Pro directly into late-stage clinical trials, leveraging its potential as the first oral, disease-modifying treatment for PAH. As a prodrug of imatinib, IkT-001Pro builds upon existing scientific understanding while potentially offering improved therapeutic properties.
"This substantial financing from specialized healthcare investors validates our approach to developing IkT-001Pro as a potential breakthrough therapy for PAH patients," said Milton Werner, Ph.D., President and CEO of Inhibikase Therapeutics. "The NME designation from the FDA further strengthens our development pathway."

Broader Pipeline Development

While advancing IkT-001Pro in PAH, Inhibikase maintains a diverse pipeline targeting protein kinase inhibitor therapeutics. The company is simultaneously progressing other programs, including their '201' trial evaluating risvodetinib in Parkinson's disease, with results expected in Q4 2024.
The secured funding will primarily support the late-stage development of IkT-001Pro while ensuring the company has sufficient resources to advance its broader therapeutic portfolio. This positions Inhibikase to potentially deliver multiple transformative treatments across several high-need therapeutic areas.
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Reference News

[1]
Inhibikase Therapeutics, Inc. (IKT)
finance.yahoo.com · Jan 23, 2025

Inhibikase Therapeutics secured up to $275M in financing, advancing IkT-001Pro into late-stage trials for Pulmonary Arte...

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