Epigenetic Reprogramming in Relapse/Refractory AML
Part of paid clinical trials in Los Angeles, California.
- Sponsor
- Therapeutic Advances in Childhood Leukemia Consortium
- Study ID
- NCT03263936
- Phase
- PHASE1
- Status
- Completed
Conditions
- Acute Myelogenous Leukemia
Eligibility Criteria
- Sex
- ALL
- Age
- 1 Year - 25 Years
- Healthy Volunteers
- Not accepted
Interventions
- Decitabine — DRUGDose Level #0: 5 mg/m2 Dose Level #1: 7.5 mg/m2 Dose Level #2: 10 mg/m2 Dose Level #3: 15 mg/m2 Dose Level #4: 20 mg/m2 given IV over \_\_ hour on days 1 through 5
- Vorinostat — DRUGAge \<18: 180 mg/m2/day once daily PO. Age≥18: 200 mg twice daily PO.
- Filgrastim (G-CSF) — DRUGGiven on days 5 until evidence of ANC recovery (\>500/µL)5µg/kg/dose IV or SQ (starting at hour 0)
- Fludarabine — DRUG30 mg/m2/day IV over 30 minutes (starting at Hour 0 - Immediately after G-CSF)
- Cytarabine — DRUG2000 mg/m2/day (Starting at Hour 0.5),IV over 3 hours, days 6-10
Study Details
This is a pilot study using decitabine and vorinostat before and during chemotherapy with fludarabine, cytarabine and G-CSF (FLAG).
Key Dates
- Start date
- Jul 11, 2017
- Status verified
- May 2023
- Primary completion
- Jul 9, 2020
- Completion
- Feb 10, 2022
Study Design
- Enrollment
- 37 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Other: Otherdecitabine, vorinostat, fludarabine, high dose cytarabine, filgrastim (G-CSF)
Primary Outcome Measure
The Dose of Decitabine That Can be Safely Given With Vorinostat, Fludarabine, High Dose Cytarabine and G-CSF (FLAG) [ Time Frame: during course 1 DLT evaluation period, approx 9 weeks ]
Locations (28)
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