Houston company announces FDA acceptance of ALS drug application
HOUSTON, TX – A Houston-based clinical-stage biotechnology company (NASDAQ: COYA) announced that the U.S. Food and Drug Administration (FDA) has accepted its Investigational New Drug (IND) application for COYA 302, a biologic therapy being developed for the treatment of amyotrophic lateral sclerosis (ALS).
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The FDA’s acceptance enables the company to begin a Phase 2 multicenter, double-blind, placebo-controlled clinical study evaluating the efficacy and safety of COYA 302 in ALS patients. The approval also triggers a $4.2 million milestone payment from its partner, Dr. Reddy’s Laboratories Ltd.
According to the company, COYA 302 is a proprietary combination therapy designed to enhance the anti-inflammatory function of regulatory T cells and suppress inflammat...









