27Jan 2024
Heron Therapeutics gets US FDA nod for Zynrelef indication expansion

Heron Therapeutics gets US FDA nod for Zynrelef indication expansion

Heron Therapeutics, Inc. has received FDA approval to expand the indication for Zynrelef, its extended-release solution, to include soft tissue and orthopaedic surgical procedures, covering an estimated 13 million additional procedures annually. This represents an 86% increase over prior indicated procedures. Zynrelef, already approved for various surgical procedures, demonstrated superiority to the standard-of-care bupivacaine solution in phase 3 studies. The expanded indication is expected to positively impact patient care, providing a versatile and effective solution for managing postoperative pain across a broader range of surgical procedures. The approval follows successful studies for various surgical interventions with no identified safety issues.

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