Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT06287229
PHASE1/PHASE2

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

View on ClinicalTrials.gov

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

DRUG

Blinatumomab

Given by Infusion

DRUG

Inotuzumab Ozogamicin

Given by IV

DRUG

Hyper-CVAD

Given by IV Participants younger than 60 years of age, you will receive hyper-CVAD.

DRUG

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