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Heron Therapeutics’ Aponvie (HTX-019) Receives the US FDA’s Approval for the Prevention of Postoperative Nausea and Vomiting

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Heron Therapeutics’ Aponvie (HTX-019) Receives the US FDA’s Approval for the Prevention of Postoperative Nausea and Vomiting

Shots:

  • The US FDA has approved Aponvie injectable emulsion for IV use to prevent postoperative nausea & vomiting in adults
  • The approval was based on the 2 clinical studies evaluating aprepitant vs IV ondansetron in patients with PONV. The results showed that aprepitant was more effective in preventing vomiting with ~50% fewer patients vomiting in the first 24 & 48hrs., after open abdominal surgery
  • The P-I trial showed that 32mg of aprepitant as a 30-second IV injection was bioequivalent to aprepitant (40mg), was well tolerated with a comparable safety profile. The product is ready-to-use, easy to administer, innovative IV formulation & was supplied in a single-dose vial containing 32mg of aprepitant

Ref: PRNewswire | Image: Heron Therapeutics

Click here to­ read the full press release 

Senior Editor

Neha is a Senior Editor at PharmaShots. She is passionate and very enthusiastic about recent updates and developments in the life sciences and pharma industry. She covers Biopharma, MedTech, and Digital health segments along with different reports at PharmaShots. She can be contacted at connect@pharmashots.com.

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