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Phase Ib/II Study Assessing the Clinical Activity and Safety of Brexucabtagene Autoleucel as a Consolidation in Patients With Relapsed/Refractory (R/R) and Newly Diagnosed B-cell Acute Lymphocytic Leukemia (ALL) Post Cytoreduction With Mini-HCVD-inotuzumab-blinatumomab/HCVAD-inotuzumab-blinatumomab
Sponsor: M.D. Anderson Cancer Center
Summary
To learn about the safety of giving the drug brexucabtagene autoleucel to participants with relapsed/refractory B-cell ALL after treatment with inotuzumab ozogamicin, blinatumomab, and either hyper-CVAD or mini-hyper-CVD. Also, to learn if giving brexucabtagene autoleucel to patients with relapsed/refractory or high-risk, newly diagnosed B-cell ALL after treatment with inotuzumab ozogamicin, blinatumomab, and either hyper-CVAD or mini-hyper-CVD can help to control the disease.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
40
Start Date
2024-07-11
Completion Date
2030-12-31
Last Updated
2026-02-17
Healthy Volunteers
No
Interventions
Blinatumomab
Given by Infusion
Inotuzumab Ozogamicin
Given by IV
Hyper-CVAD
Given by IV Participants younger than 60 years of age, you will receive hyper-CVAD.
Mini-hyper-CVD
Given by IV Participants 60 years of age or older, you will receive mini-hyper-CVD
Locations (1)
MD Anderson Cancer Center
Houston, Texas, United States