Viridian Therapeutics Inc. Announces Breakthrough Therapy Designation for Veligrotug, Paving Way for Priority Review
Viridian Therapeutics, Inc., a biopharmaceutical company specializing in treatments for serious and rare diseases, has announced a significant milestone in the regulatory review process for its drug veligrotug. The company is on track to submit a Biologics License Application $(BLA.AU)$ for veligrotug, an anti-IGF-1R antibody developed for treating active thyroid eye disease (TED), in the second half of 2025. Veligrotug, which recently received Breakthrough Therapy Designation, is anticipated for a U.S. commercial launch in 2026, pending approval. This designation supports its eligibility for Priority Review due to its demonstrated effectiveness in improving and resolving symptoms of TED in clinical trials.
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: 20250520329293) on May 20, 2025, and is solely responsible for the information contained therein.
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