Active, not recruitingPHASE1, PHASE2NCT05226455
Venetoclax in Patients With MDS or AML in Relapse After AHSCT
Studying Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Groupe Francophone des Myelodysplasies
- Principal Investigator
- Thomas CLUZEAU, PHDCHU de Nice - Hôpital l'Archet I
- Intervention
- venetoclax + azacitidine +/- donor lymphocyte infusion(drug)
- Enrollment
- 55 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2022 – 2027
Study locations (11)
- CHU d'Angers, Angers, France
- CHU de Grenoble, Grenoble, France
- Hôpital Dupuytren, Limoges, France
- Hôpital Saint-Eloi, Montpellier, France
- CHU Hôtel Dieu, Nantes, France
- Hôpital l'Archet I, Nice, France
- Hôpital Saint louis, Paris, France
- CHU de Haut-Lévèque, Pessac, France
- Centre Hospitalier Lyon-Sud, Pierre-Bénite, France
- Centre Henri Becquerel, Rouen, France
- IUCT Oncopole, Toulouse, France
Collaborators
AbbVie
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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