- Theravance Biopharma settled Hatch-Waxman patent litigation over YUPELRI (revefenacin) inhalation solution with Mankind Pharma, clearing a path for a future generic launch.
- Settlement grants Mankind a royalty-free, non-exclusive US license to launch its generic on or after April 23, 2039.
- Agreement resolves claims tied to Mankind ANDA filing that sought approval to sell a generic before expiry of patents asserted by Theravance, with Viatris unit Mylan as exclusive US sublicencee.
- All pending Hatch-Waxman litigation related to YUPELRI has been resolved.
- Deal remains subject to US Department of Justice, Federal Trade Commission review.
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. Theravance Biopharma Inc. published the original content used to generate this news brief via EDGAR, the Electronic Data Gathering, Analysis, and Retrieval system operated by the U.S. Securities and Exchange Commission (Ref. ID: 0001104659-26-036870), on March 30, 2026, and is solely responsible for the information contained therein.
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