A First-In-Human, Open-Label, Escalating Multiple-Dose Study to Evaluate the Safety, Toxicity, and Pharmacokinetics of BTX-A51 Alone and in Combination With Azacitidine in Patients With Relapsed or Refractory Acute Myeloid Leukemia or High-Risk Myelodysplastic Syndrome
Latest Information Update: 22 Mar 2024
At a glance
- Drugs BTX A51 (Primary) ; Azacitidine; Azacitidine
- Indications Acute myeloid leukaemia; Myelodysplastic syndromes
- Focus Adverse reactions; First in man
- Sponsors BioTheryX
Most Recent Events
- 08 Feb 2024 Planned number of patients changed from 50 to 80.
- 08 Feb 2024 Planned End Date changed from 1 Mar 2025 to 1 Mar 2027.
- 08 Feb 2024 Planned primary completion date changed from 1 Mar 2023 to 1 Mar 2026.