U.S. FDA Approves Pfizer’s HYMPAVZI for the Treatment of Two Additional Hemophilia A or B Patient Populations with Significant Medical Need
The FDA approved an expanded indication for Pfizer’s HYMPAVZI to treat hemophilia A or B patients aged 12 and older with inhibitors, as well as pediatric patients aged 6 to 11 with or without inhibitors. This approval is supported by Phase 3 trial data showing a 93% reduction in annualized bleeding rates for inhibitor-positive patients compared to standard bypassing agents.
Key figures
- Drug Name
- HYMPAVZI (marstacimab-hncq)
- Phase Of Trial
- Phase 3
- Abrr bypassing agents
- 19.8
- Abrr hympavzi inhibitors
- 1.4
- Abrr pediatric inhibitors
- 1.4
- Abrr reduction inhibitors
- 93%
- Global hemophilia patients
- 800,000
- Abrr pediatric no inhibitors
- 1.8
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