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Mineralys Therapeutics Submits NDA for Lorundrostat to FDA

Reuters01-06

Mineralys <a href="https://laohu8.com/S/LENZ">Therapeutics</a> Submits NDA for Lorundrostat to FDA

Mineralys Therapeutics Inc. has filed a New Drug Application (NDA) with the U.S. Food and Drug Administration (FDA) for lorundrostat, following the successful completion of three positive clinical trials in 2025. The NDA submission marks a key regulatory milestone for the company as it seeks approval for lorundrostat, a drug candidate designed to treat hypertension and related comorbidities. The NDA is supported by data demonstrating lorundrostat’s safety, 24-hour blood pressure control, and efficacy across diverse patient populations.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Mineralys Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 9620090) on January 06, 2026, and is solely responsible for the information contained therein.

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