Organogenesis Confirmed to Start FDA License Application for ReNu

Dow Jones
2025/12/16

By Katherine Hamilton

 

Organogenesis received confirmation to initiate a license application with the Food and Drug Administration for its knee condition treatment ReNu.

The regenerative tissue company said Monday it plans to initiate a rolling Biologics License Application for ReNu before the end of December.

Shares gained 9% to $5.28 in after-hours trading.

The plans come after a planned Type-B meeting with the FDA, which was completed Monday, Organogenesis said.

Organogenesis has done two large Phase 3 trials of ReNu, plus a separate randomized controlled trial.

ReNu is designed to treat people with symptomatic knee osteoarthritis, a degenerative condition that causes knee pain. It affects 31.1 million Americans and is ranked among the most common causes of disability and poor quality of life, Organogenesis said.

 

Write to Katherine Hamilton at katherine.hamilton@wsj.com

 

(END) Dow Jones Newswires

December 15, 2025 17:11 ET (22:11 GMT)

Copyright (c) 2025 Dow Jones & Company, Inc.

应版权方要求,你需要登录查看该内容

免责声明:投资有风险,本文并非投资建议,以上内容不应被视为任何金融产品的购买或出售要约、建议或邀请,作者或其他用户的任何相关讨论、评论或帖子也不应被视为此类内容。本文仅供一般参考,不考虑您的个人投资目标、财务状况或需求。TTM对信息的准确性和完整性不承担任何责任或保证,投资者应自行研究并在投资前寻求专业建议。

热议股票

  1. 1
     
     
     
     
  2. 2
     
     
     
     
  3. 3
     
     
     
     
  4. 4
     
     
     
     
  5. 5
     
     
     
     
  6. 6
     
     
     
     
  7. 7
     
     
     
     
  8. 8
     
     
     
     
  9. 9
     
     
     
     
  10. 10