Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07223021

A Study of Fludarabine Dosing in Children and Young Adults With B-cell Acute Lymphoblastic Leukemia

Improving EveNt Free Survival by Optimizing FLUdarabine Exposure During LymphodepletioN for CAR T CEll Therapy: a Randomized, Multi-center Study of Children and Young Adults With B-cell Acute Lymphoblastic Leukemia (INFLUENCE)

Status
Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
130 (estimated)
Sponsor
Memorial Sloan Kettering Cancer Center · Academic / Other
Sex
All
Age
1 Year
Healthy volunteers
Not accepted

Summary

The researchers are doing this study to find out whether PK-targeted fludarabine is an effective Lymphodepletion (LD) chemotherapy approach for people with relapsed/refractory B-cell acute lymphoblastic leukemia (B-ALL) who will receive tisagenlecleucel CAR T-cell therapy. The researchers will compare PK-targeted fludarabine dosing with standard fludarabine dosing to see which treatment approach is more effective. The researchers will also look at whether PK-targeted fludarabine dosing is feasible (practical), the side effects of the study treatment, and how the study treatment affects people's quality of life. The researchers will measure quality of life by having participants complete questionnaires.

Conditions

Interventions

TypeNameDescription
DRUGFludarabineFludarabine 30 mg/m2/dose x 4 doses on days -6 to -3 (or -7 to -4)
DRUGCyclophosphamideAll patients will receive Cyclophosphamide 500 mg/m2 IV on days -6 and -5 (or -7 and -6).
DRUGFludarabineTargeted fludarabine LD: Fludarabine 40 mg/m2/dose x 2 doses on days -6 and -5 (or -7 and -6), with doses on days -4 and -3 (or -5 and -4, if starting lymphodepletion on day -7) adjusted based on PK analysis to target a cumulative area under the curve (AUC) of 18 mg\*h/L (range 17.5-18.5mg\*h/L)
BIOLOGICALCAR-Twill be infused based on institutional guidelines.

Timeline

Start date
2025-10-20
Primary completion
2028-10-01
Completion
2028-10-01
First posted
2025-10-31
Last updated
2026-03-30

Locations

3 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT07223021. Inclusion in this directory is not an endorsement.