Adding Venetoclax to the High-dose Chemotherapy Regimen Prior to Mismatche Allogeneic Stem Cell Transplant
Withdrawn before enrolling · Phase 2
Conditions studied: Acute Myeloid Leukemia, Myelodysplastic Syndromes
In brief
Patients eligible for a mismatch allogeneic stem cell transplant will receive Venetoclax daily for 7 days prior to transplant in addition to the following chemotherapy regimen: Decitabine daily for 5 days, Fludarabine daily for 5 days, and Busulfan daily for 2 days followed by 1 day of total body irradiation. Stem cell transplant will occur thereafter.
Key facts
- Study ID
- NCT06337331
- Run by
- Northside Hospital, Inc.
- People needed
- 0
- Starts
- 2024-08-31
- Expected to finish
- 2027-08-31
- Last updated by the study team
- 2024-06-14
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Availability of a 4/8 - 6/8 HLA-matched related donor or a 7/8 HLA-matched unrelated donor
- Receiving first allogeneic transplant
- KPS >/= 70%
- MDS associated with TP53 mutation AND R-IPSS high or very high risk at diagnosis OR
- AML with adverse risk cytogenetics or molecular abnormalities according to the 2017 ELN risk stratification OR pre-transplant MRD by either flow cytometry, cytogenetics or FISH
- Less than 5% myeloblasts in the marrow pre-transplant
You may not qualify if…
- Poor cardiac function defined as LVEF <45%
- Poor pulmonary function defined as FEV1, FVC, or DLCO <50% predicted
- Poor liver function defined as bilirubin >/=2.5mg/dL, AST/ALT >3xULN
- Poor renal function defined as creatinine >/=2.0mg/dL or CrCl <40mL/min
- Ongoing or active systemic infection, active Hepatitis B or C virus infection, or known HIV positivity
- Patient requiring treatment with a moderate or strong inhibitor or inducer of CYP3A4 or a P-gp inhibitor within 7 days prior to starting preparative chemotherapy through Day +4 post-transplant
Where it is running
- Caitlin Guzowski — Atlanta, Georgia, United States
Full record on ClinicalTrials.gov
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