Viridian Therapeutics Submits BLA to FDA for Veligrotug in Thyroid Eye Disease

Reuters11-03

Viridian <a href="https://laohu8.com/S/LENZ">Therapeutics</a> Submits BLA to FDA for Veligrotug in Thyroid Eye Disease

Viridian Therapeutics Inc. has announced the successful submission of a Biologics License Application (BLA) to the U.S. Food and Drug Administration (FDA) for veligrotug, its investigational therapy for thyroid eye disease (TED). The submission is supported by positive results from two pivotal phase 3 trials, THRIVE and THRIVE-2, which met all primary and secondary endpoints. Viridian has also requested Priority Review, which, if granted, could lead to a potential commercial launch of veligrotug in mid-2026, pending FDA approval. No grant or funding from multiple organizations was mentioned in the announcement.

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. Viridian Therapeutics Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 20251028721424) on November 03, 2025, and is solely responsible for the information contained therein.

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