Novo Nordisk has successfully met the primary endpoints in its HIBISCUS trial for etavopivat. The company intends to file for regulatory approval of the sickle cell disease treatment later this year.
- Phase 3 HIBISCUS trial reached co-primary endpoints
- Etavopivat is the experimental therapy for SCD
- Regulatory approval filing planned for 2026
- Diversifies NVO pipeline beyond GLP-1 medications
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