Venetoclax and Decitabine in R/R T-ALL
- Sponsor
- Seoul National University Hospital
- Study ID
- NCT06712121
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- T Lymphoblastic Leukemia/Lymphoma
Eligibility Criteria
- Sex
- ALL
- Age
- 19 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- decitabine plus venetoclax — DRUGdecitabine 20mg/m2 for 7 days venetoclax 400mg daily for 21 days
Study Details
The goal of this phase 2 clinical trial is to test the efficacy of decitabine and venetoclax combination chemotherapy in relapsed or refractory adult T-cell acute lymphoblastic leukemia/lymphoblastic lymphoma. This study use a modified regimen of decitabine and venetoclax.
Key Dates
- Start date
- Jan 30, 2025
- Status verified
- Jan 2026
- Primary completion
- Aug 31, 2027
- Completion
- Aug 31, 2028
Study Design
- Enrollment
- 28 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: decitabine and venetoclax armarm treated with venetoclax plus decitabine
Primary Outcome Measure
The rate of composite Complete remission [ Time Frame: 1 year ]
Central Contacts
- Dong-Yeop Shin, MD, PhD.82+220727209
- EunHee Park, RN