FDA grants approval for TAZVERIK
- Katrina Williams
- January 29, 2020
- No responses
Epizyme announces that U.S. Food and Drug Administration (FDA) has granted accelerated approval of TAZVERIK (tazemetostat) for the treatment of adults and pediatric patients age 16 years and older with metastatic or locally advanced epithelioid sarcoma not eligible for resection, based on overall response rate and duration of response in a Phase 2 clinical trial. You can view the U.S Full Prescribing information at www.epizyme.com.