Study of Venetoclax, a BCL2 Antagonist, for Patients With Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN)
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Dana-Farber Cancer Institute
- Study ID
- NCT03485547
- Phase
- PHASE1
- Status
- Completed
Conditions
- Blastic Plasmacytoid Dendritic Cell Neoplasm
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Venetoclax — DRUGVENCLEXTA targets BCL-2 in order to help restore the process of apoptosis. Through apoptosis, your body allows cancer cells and normal cells to self-destruct
Study Details
This research study is studying a drug as a possible treatment for BPDCN. The intervention involved in this study is: Venetoclax
Key Dates
- Start date
- Aug 23, 2018
- Status verified
- Jan 2026
- Primary completion
- Jan 10, 2022
- Completion
- Apr 16, 2025
Study Design
- Enrollment
- 5 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Venetoclax* Venetoclax is administered on a daily basis orally. * The investigators will use a modified 3+3 with a de-escalation dose level design to establish the appropriate and tolerable dose of venetoclax.
Primary Outcome Measure
Dose Limiting Toxicity [ Time Frame: 2 years ]
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Dana Farber Cancer Institute | Boston | Massachusetts | 02215 | - |
| MD Anderson Cancer Center | Houston | Texas | 77030 | - |
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