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Heron Therapeutics' ZYNRELEF (HTX-011) Receives the US FDA's Approval for the Management of Postoperative Pain

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Heron Therapeutics' ZYNRELEF (HTX-011) Receives the US FDA's Approval for the Management of Postoperative Pain

Shots:

  • The US FDA approved Zynrelef (bupivacaine and meloxicam) extended-release solution for postsurgical analgesia in patients with soft tissue or periarticular instillation for 72 hrs after a bunionectomy- open inguinal herniorrhaphy and total knee arthroplasty
  • The approval is based on data from the P-III studies assessing Zynrelef vs bupivacaine solution in 1000 patients which demonstrated superiority to bupivacaine solution & sustained postoperative pain relief for up to 72 hrs and decreased the need for opioids
  • Zynrelef is the 1st FDA-approved extended-release dual-acting local anesthetic and is approved in 31 EU countries. The company plans to launch Zynrelef in Jul 2021

  Ref: PRNewswire | Image: BioSpace

Click here to­ read the full press release 

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