
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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