First-In-Human, Open Label, Dose Escalation Study to Evaluate Safety, PK and PD of ABD-3001 as Monotherapy in Relapsed/Refractory Acute Myeloid Leukemia or High/Very-high Risk Myelodysplastic Syndromes Patients, Ineligible for Intensive or New Generation Targeted Therapy
Latest Information Update: 17 Mar 2025
At a glance
- Drugs ABD 3001 (Primary)
- Indications Acute myeloid leukaemia; Myelodysplastic syndromes
- Focus Adverse reactions; First in man
- Acronyms ODYSSEY
- Sponsors Advanced BioDesign
- 04 Mar 2025 According to an Advanced Biodesign media release, the first patient has been successfully treated for 3 cycles of treatment in this trial.
- 11 Nov 2024 Planned number of patients changed from 7 to 36.
- 28 Oct 2024 According to an Advanced BioDesign media release, topline data is expected during the third quarter of this year.