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NCT07223021RecruitingPhase 3

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)

Source: ClinicalTrials.gov · Last updated 5 Oct 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
130 (estimated)
First submitted
28 Oct 2025
Start date
20 Oct 2025
Primary completion date
31 Oct 2028
Lead sponsor
Memorial Sloan Kettering Cancer Center
NCT number
NCT07223021
EU CT number
2025-523096-34-00

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 130
  • From 20 Oct 2025 to the primary completion date, 31 Oct 2028
  • 8 sites in 4 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Have a known immediate or delayed hypersensitivity reaction or idiosyncrasy to the study drugs, or drugs chemically related to study treatment or excipients that contraindicate their participation, including fludarabine, cyclophosphamide and tisagenlecleucel.

Lab values

  • Clinically significant active and uncontrolled infection confirmed by clinical evidence, imaging, or positive laboratory tests (e.g., blood cultures, PCR for DNA/RNA etc.)

Other

  • Patients with tisagenlecleucel that is deemed out of specification (OOS) will be excluded from this protocol
  • Patient/parent/guardian unable to give informed consent or unable to comply with the treatment protocol.
  • Pregnant or lactating women

Who the study is looking for

  • Patients with B-ALL and eligible to receive commercial tisagenlecleucel.
  • Patient's weight \> 9 kg at time of lymphodepleting chemotherapy
  • Adequate organ function at time of LD is required and is defined:
    • Hepatic: Serum bilirubin ≤ 2 mg/dL, unless benign congenital hyperbilirubinemia
    • Hepatic: AST and ALT \< 5x the upper limit of normal for age, unless thought to be leukemic disease-related
    • Renal: Calculated glomerular filtration rate (GFR) ≥ 70 ml/min/1.73m\^2. (based on Schwartz formula GFR (mL/min/1.73 m²) = (36.2 × Height in cm) / Creatinine in mg/dL
    • Cardiac: LVEF ≥ 50% by multi-gated acquisition scan (MUGA), resting echocardiogram, or cardiac magnetic resonance imaging (MRI) within 6 weeks of screening
    • Pulmonary: Oxygen saturation as recorded by pulse oximetry of ≥ 90% on room air
  • Adequate performance status:
    • Age ≥ 16 years: ECOG ≤ 1 or Karnofsky \> 60% at treatment
    • Age \< 16 years: Lansky ≥ 60% at treatment
  • Willing to participate as research subject and provide written informed consent from parents/legal representative, patient, and age-appropriate assent as appropriate before any study specific screening procedures are conducted, according to local, regional or national law and legislation.

Age in the registry: 1 year to 64 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (8)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Universitaet Muenster
Coordinator of this site? Confirm its status
MuensterGermanyNot yet recruiting
Hospital Sant Joan De Deu Barcelona
Coordinator of this site? Confirm its status
Esplugues de LlobregatSpainNot yet recruiting
Prinses Maxima Centrum voor Kinderoncologie B.V.
Coordinator of this site? Confirm its status
UtrechtNetherlandsRecruiting
Cincinnati Children's Hospital Medical Center (Data Collection Only)
Coordinator of this site? Confirm its status
CincinnatiUnited StatesRecruiting
Texas Children's Hospital (Data Collection)
Coordinator of this site? Confirm its status
HoustonUnited StatesRecruiting
Baylor College Medical Center (Data Collection Only)
Coordinator of this site? Confirm its status
HoustonUnited StatesNot yet recruiting
Memorial Sloan-Kettering Cancer Center
Coordinator of this site? Confirm its status
New YorkUnited StatesRecruiting
Children's Hospital of Philadelphia (Data Collection Only)
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.