A Phase 1b, Open Label, Multi-center, Dose Optimization and Dose Expansion Study to Assess the Safety and Efficacy of DFV890 in Adult Patients With Myeloid Diseases
Latest Information Update: 30 May 2025
At a glance
- Drugs DFV 890 (Primary)
- Indications Chronic myelomonocytic leukaemia; Myelodysplastic syndromes
- Focus Adverse reactions
- Sponsors Novartis Pharmaceuticals
Most Recent Events
- 16 May 2025 Planned End Date changed from 30 Jun 2026 to 1 Feb 2027.
- 16 May 2025 Planned primary completion date changed from 30 Jun 2026 to 29 Jan 2027.
- 08 Jan 2024 Planned End Date changed from 30 Jun 2025 to 30 Jun 2026.