- Commercial-stage biotech Heron Therapeutics, Inc. ( NASDAQ: HRTX ) announced Friday that the FDA approved its intravenous injection Aponvie (aprepitant) for the prevention of postoperative nausea and vomiting (PONV) in adults. HRTX shares are currently on hold for trading.
- It is estimated that 30% of patients who have received general anesthesia and up to 80% of high-risk patients experience PONV.
- "This marks an important milestone for our expanding acute care portfolio and is a testament to our ongoing commitment to developing innovative solutions to help improve the overall patient experience after surgery," HRTX Chief Executive Barry Quart noted.
- In Nov. 2021, the company submitted the New Drug Application for Aponvie targeting PONV in adults, and later the FDA accepted the marketing application granting Sep. 17 as the PDUFA date.
For further details see:
Heron wins FDA nod for post-operative agent to address nausea and vomiting