A Study of Tagraxofusp in Combination With Venetoclax and Azacitidine in Adults With Untreated CD123+ Acute Myeloid Leukemia Who Cannot Undergo Intensive Chemotherapy
Part of paid clinical trials in Los Angeles, California.
- Sponsor
- Stemline Therapeutics, Inc.
- Study ID
- NCT06456463
- Phase
- PHASE2
- Status
- Active Not Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Tagraxofusp — DRUGTagraxofusp will be administered by intravenous infusion for 3 consecutive days during each 28-day cycle.
- Venetoclax — DRUGVenetoclax will be administered as an oral tablet (400 milligrams \[mg\]) daily, with ramp up in Cycle 1, and should be continued at target dose (400 mg) for the remainder of Cycle 1 and subsequent cycles of 28 days each.
- Azacitidine — DRUGAzacitidine will be administered subcutaneously or by intravenous infusion (75 milligrams/square meter) over 7 days of each 28-day cycle, per institutional guidelines/physician choice.
Study Details
This study will be divided into 2 parts (Part 1 and Part 2). Part 1 will evaluate 2 doses of tagraxofusp (9 and 12 micrograms/kilogram/day \[μg/kg/day\]), used in combination with venetoclax and azacitidine, to determine the dose for Part 2. This determined dose, in combination with venetoclax and azacitidine, will then be further evaluated in Part 2 in 2 cohorts (TP53 mutated and TP53 wild type). Both parts will be conducted in participants with previously untreated CD123+ AML who are ineligible for intensive chemotherapy.
Key Dates
- First listed
- Jun 13, 2024
- Start date
- Jan 14, 2025
- Status verified
- Aug 2026
- Primary completion
- Feb 9, 2028
- Completion
- Feb 11, 2030
Study Design
- Enrollment
- 85 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: Part 1 - Tagraxofusp (9 μg/kg/day)Participants will receive tagraxofusp in combination with venetoclax and azacitidine.
- Experimental: Part 1 - Tagraxofusp (12 μg/kg/day)Participants will receive tagraxofusp in combination with venetoclax and azacitidine.
- Experimental: Part 2 - Tagraxofusp (Selected Dose) and TP53 Wild TypeParticipants (TP53 wild type) will receive tagraxofusp in combination with venetoclax and azacitidine.
- Experimental: Part 2 - Tagraxofusp (Selected Dose) and TP53 MutatedParticipants (TP53 mutated) will receive tagraxofusp in combination with venetoclax and azacitidine.
Primary Outcome Measure
Part 1: Determination of Part 2 Selected Dose of Tagraxofusp When Administered in Combination with Venetoclax and Azacitidine [ Time Frame: Cycles 1-4 (up to 112 days; 28 days/cycle) ]
Locations (24)
Find similar trials in Los Angeles, CA
Related Studies
- Monitoring Minimal Residual Disease of Patients With Acute Myelogenous Leukemia or High Grade Myelodysplastic SyndromeRecruiting · University of Rochester · Rochester, New York
- Cladribine, Idarubicin, Cytarabine, and Venetoclax in Treating Patients With Acute Myeloid Leukemia, High-Risk Myelodysplastic Syndrome, or Blastic Phase Chronic Myeloid LeukemiaPHASE2 · Recruiting · M.D. Anderson Cancer Center · Houston, Texas
- PET/MRI, 18F-FDG PET/CT and Whole Body MRI in Finding Extramedullary Myeloid Leukemia in Patients With Newly Diagnosed Acute Myeloid LeukemiaPHASE1 · Recruiting · M.D. Anderson Cancer Center · Houston, Texas
- KIR Favorable Mismatched Haplo Transplant and KIR Polymorphism in ALL/AML/MDS Allo-HCT ChildrenPHASE2 · Enrolling By Invitation · Michael Pulsipher · Los Angeles, California