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Coya Therapeutics, a clinical-stage biotech company, has received FDA clearance for its IND application for COYA 302 in amyotrophic lateral sclerosis (ALS). The company is also expanding its pipeline beyond ALS with an IND filing for frontotemporal dementia expected in late 2025. Strategic partnerships, including with Dr. Reddy's Laboratories, provide financial support and expertise. Key milestones for 2025 include ALS trial initiation, FTD data readouts, and new preclinical results across multiple programs.
Coya Therapeutics, a clinical-stage biotechnology company, has made significant strides in its mission to address neurodegenerative diseases. On September 3, 2025, the company received FDA clearance for its Investigational New Drug (IND) application for COYA 302 in amyotrophic lateral sclerosis (ALS). This clearance enables the initiation of a pivotal Phase 2 clinical trial, marking a crucial milestone in the development of potential therapies for ALS [1].
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