FDA Grants Fast Track Designation to Kymera Therapeutics’ KT-621 for Atopic Dermatitis

Reuters12-11

FDA Grants <a href="https://laohu8.com/S/FTRK">Fast Track</a> Designation to Kymera <a href="https://laohu8.com/S/LENZ">Therapeutics</a>' KT-621 for Atopic Dermatitis

Kymera Therapeutics Inc. has announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation to KT-621, its first-in-class oral STAT6 degrader, for the treatment of moderate to severe atopic dermatitis. This designation is based on positive results from the KT-621 BroADen Phase 1b trial in atopic dermatitis patients. Fast Track status is expected to facilitate the development and expedite the review process for KT-621. The ongoing BROADEN2 Phase 2b trial for atopic dermatitis is expected to report data by mid-2027, and a Phase 2b trial in asthma is set to begin in the first quarter of 2026.

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. Kymera Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9600507-en) on December 11, 2025, and is solely responsible for the information contained therein.

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