Organogenesis completes FDA BLA submission for ReNu knee osteoarthritis therapy
PUBT · 04/28 21:04
Share
Listen to the news
- Organogenesis completed rolling FDA Biologics License Application submission for ReNu, treatment candidate for symptomatic knee osteoarthritis.
- Submission started December 2025 with non-clinical modules; clinical modules plus CMC modules now filed.
- ReNu received FDA RMAT designation for knee osteoarthritis in 2021.
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. Organogenesis Holdings Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202604281630PRIMZONEFULLFEED9708902) on April 28, 2026, and is solely responsible for the information contained therein.
Disclaimer:This article represents the opinion of the author only. It does not represent the opinion of Webull, nor should it be viewed as an indication that Webull either agrees with or confirms the truthfulness or accuracy of the information. It should not be considered as investment advice from Webull or anyone else, nor should it be used as the basis of any investment decision.
What's Trending
No content on the Webull website shall be considered a recommendation or solicitation for the purchase or sale of securities, options or other investment products. All information and data on the website is for reference only and no historical data shall be considered as the basis for judging future trends.
Copyright © 2026 Webull. All Rights Reserved