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NCT Number: NCT03937544

Intravenous Autologous CD19 CAR-T Cells for R/R B-ALL

This is Phase II / III, Prospective, single arm, Open Label Study to Evaluate Safety and Efficacy of Intravenous Autologous CD19 CAR-T Cells for Relapsed / Refractory B-Acute Lymphoblastic Leukaemia

Recruiting

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Key information

Age range

13 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with relapsed/refractory B-ALL in accordance with World Health Organization (WHO) classification by virtue of BM morphology, flow cytometry, cytogenetics and molecular genetics
  • Age between ≥13 to ≤ 65 years
  • No detectable leukaemia in the CSF (CNS-1)
  • CNS leukaemia without clinically evident neurological symptoms (CNS-2; with <5 WBC per μL and cytology positive for blasts)
  • Adequate organ function as defined by a creatinine clearance > 50 ml/min, serum total bilirubin < 5 times the normal value, left ventricular ejection fraction > 40%
  • ECOG performance status ≤ 2
  • Life expectancy > 3 months
  • Post allogeneic HSCT must be ≥ Day +100 with no evidence of active GVHD and not receiving immunosuppression
  • Female patients of child bearing age must have negative pregnancy test and is on highly effective contraception methods
  • Male patients must use highly effective contraception methods

Exclusion criteria

  • Patients with CNS-3 leukaemia.
  • Active cancer (other than B-ALL).
  • Evidence of severe lung, heart (NYHA class III/IV, arrhythmia, AV block, uncontrolled hypertension), liver, or renal failure or severe neurologic disorder.
  • Presence of active autoimmune disease or atopic allergy.
  • HIV serology positivity.
  • Active Hepatitis B or C infection as evidenced by quantitative viral PCR assay.
  • Uncontrolled sepsis
  • Pregnant / nursing female.
  • Ongoing prednisolone > 1mg/kg daily or equivalent.
  • Chemotherapy immunotherapy in the recent 4 weeks such as allogeneic cellular therapy weeks, anti-GVHD therapy.

Treatment and study plan

CD19 CAR-T cells

Biological

CD19 CAR-T cells will be administered after completion of the lymphodepletion chemotherapy.

Cyclophosphamide

Drug

Patients will receive lymphodepleting chemotherapy consisting of Cyclophosphamide 250 - 300 mg/m2/day IV(Day -5, Day -4, Day -3 ).

Fludarabine

Drug

Patients will receive lymphodepleting chemotherapy consisting of Fludarabine 25-30 mg/m2/day IV (Day -5, Day -4, Day -3 ).

Primary outcomes

  1. Overall response rate (ORR)

    Time frame: Participants will be followed for the duration of the treatment, with an expected average of 3 months.

    Overall Response Rate (ORR) defined as Complete Response (CR) and CR with incomplete blood recovery (CRi) according to WHO criteria.

  2. Complete response (CR)

    Time frame: 12 Months

    Duration of response defined from the time when criteria for response (CR or CRi) are met to the first documentation of relapse or progression.

  3. CR with incomplete blood recovery (CRi).

    Time frame: 12 Months

    Duration of response defined from the time when criteria for response (CR or CRi) are met to the first documentation of relapse or progression.

Secondary outcomes

  1. Overall survival (OS)

    Time frame: 12 Months, 24 Months

    Overall Survival (OS) defined as the time from treatment to the date of death due to any cause.

  2. Progression free survival (PFS)

    Time frame: 12 Months, 24 Months

    Progression Free Survival (PFS) defined as the time from treatment to first documentation of objective leukemic progression (date of leukaemia assessment documenting progressive disease) or to death due to any cause. Progression is assessed by BM biopsy or CSF analysis according to NCCN criteria. It is assessed at Day 30 and monthly thereafter, or earlier if clinically indicated.

  3. Time to next treatment (TTNT)

    Time frame: 12 Months, 24 Months

    Time To Next Treatment (TTNT) defined as the end of study treatment until the institution of the next therapy.

  4. Percentage of adverse events

    Time frame: 30 days

    Percentage of participants with adverse events

Study contacts

Contact information is provided by the study sponsor or research team.

S Fadilah Abdul Wahid, MD, DrIntMed, PhD

CONTACT

[email protected]

+60391456450

Sponsors and collaborators

Lead sponsor

National University of Malaysia

Other

Collaborators

  • Gaia Science

Registry information

Official study title

A Phase II/III Prospective, Open Label Study to Evaluate Safety and Efficacy of Intravenous Autologous CD19 CAR-T Cells for Relapsed/ Refractory B-Acute Lymphoblastic Leukaemia

Important dates

Study start
2019
Primary completion
2027
Study completion
2027
First posted
May 3, 2019
Registry last updated
May 29, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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