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NCT Number: NCT05043571

CARTALL: Chimeric-Antigen Receptor (CAR) T-Cell Therapy for Relapsed/ Refractory T-Lineage Acute Lymphoblastic Leukaemia

The objective of this study is to assess the safety and efficacy of anti-CD7 CAR T-cells in patients with refractory or relapsed T-lineage acute lymphoblastic leukemia (T-ALL).

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Key information

Age range

6 month–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Allen Yeoh Eng Juh

Singapore, 119228

Location status: Recruiting

Location contact

Allen Yeoh, M.D

CONTACT

[email protected]

+(65) 6772 2002

Bernice Oh, M.D

SUB_INVESTIGATOR

Elaine Coustan-Smith, MS

SUB_INVESTIGATOR

Esther Chan, M.D

SUB_INVESTIGATOR

Michelle Poon, M.D

SUB_INVESTIGATOR

Noriko Shimasaki, M.D, PhD

SUB_INVESTIGATOR

Zhiwei Chen, BSc.

CONTACT

[email protected]

+(65) 6772 4406

About this study

A major obstacle to the development of effective CAR T-cells for T-cell malignancies is that the surface marker profile of malignant T-cells largely overlaps that of activated T lymphocytes. We developed a CAR T-cell approach that targets CD7, a T-cell marker highly expressed in all cases of T-cell ALL, including ETP-ALL. Its expression is also highly stable even in T-ALL cells exposed to chemotherapy. To prevent fratricide effect of the T cells, surface CD7 expression are effectively downregulated with the expression of an anti-CD7 Protein Expression Blocker (PEBL). Patients will receive anti-CD7 PEBL CART-cells. This will allow targeting the entire leukemia cell population to induce deeper and more durable remissions.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Diagnosis/ Disease define as:
  • Relapsed T-cell acute lymphoblastic leukaemia/ lymphoma as defined by:

Bone marrow disease = or > 0.01% by MRD as determined by flow cytometry

Or CNS disease as defined as > 5 WBCs/ uL in CSF with morphological evidence of blasts or biopsy proven recurrence in the eye or brain

Or Extramedullary relapse as defined by morphological evidence of blasts in the testis or any other extramedullary sites

  • Induction failure as defined by:

MRD = or > 1% by flow cytometry at the end of induction on day 33

Or Failure to achieve morphological remission defined as > 5% blasts after standard induction chemotherapy

  • Refractory disease as defined by:

MRD = or > 0.01% by flow cytometry or molecular methods during 2 or more timepoints after induction therapy

  • Minimum level of pulmonary reserve defined as Grade ≤ 1 dyspnoea and oxygen saturation (SpO2) of > 95% on room air
  • Left ventricular systolic function (LVSF) ≥ 28% confirmed by echocardiogram, or left ventricular ejection fraction (LVEF) ≥ 45% confirmed by echocardiogram within 3 months of screening
  • Karnofsky (age ≥ 16 years) or Lansky (age < 16 years) performance status ≥ 50 at screening
  • Normal Age-adjusted eGFR Creatinine Clearance within 3 months of screening
  • Alanine aminotransferase ≤ 5 times the upper limit of normal for age
  • Patients with > 99% CD7 expression on blast cells will be eligible for anti-CD7 PEBL-CAR-T cell infusion.

Exclusion criteria

  • Failure to meet any of the inclusion criteria
  • Patients who test positive on urine pregnancy testing and are pregnant or are lactating
  • Concomitant genetic syndromes associated with bone marrow failure states, such as Fanconi anaemia, Kostmann syndrome, Schwachman syndrome, or any other bone marrow failure syndrome with the exception of Down syndrome
  • Prior malignancy, except carcinoma in situ of the skin or cervix treated with curative intent and no evidence of active disease
  • Active or latent hepatitis B or hepatitis C infections within 8 weeks of screening, or any uncontrolled infection at screening
  • Positive Human Immunodeficiency Virus (HIV) test within 8 weeks of screening
  • Grade 2 to 4 acute graft-vs-host disease (GVHD) or extensive chronic GVHD
  • Received an investigational medicinal product within 30 days of screening
  • Central nervous system : Uncontrolled seizures or status epilepticus; increased intra-cranial pressure as evidenced by papilledema and CSF opening pressure > 20 cm water; decreased conscious state (any cause)

Treatment and study plan

CAR T-cell therapy

Biological

This is a single-centre, phase I study to determine the efficacy and safety of CAR T-cell therapy in patients with high-risk T-ALL, refractory or relapsed T-ALL.

Primary outcomes

  1. Proportion of participant who are flow cytometry minimal residual disease (MRD) negativity at 1 month after Anti-CD7 PEBL CAR T-cell infusion.

    Time frame: 30 days

    MRD levels will be determined by flow cytometry. The target sensitivity of flow MRD is <0.01% when available.

Secondary outcomes

  1. Proportion of participant who are minimal residual disease (MRD) negative with molecular base assay at the end of 1 month after Anti-CD7 PEBL CAR T-cell infusion.

    Time frame: 30 days

    MRD levels will be determined by molecular based MRD by Ig/TCR. PCR and oncogene fusion transcript (OFT).

  2. Proportion of patient who shows CAR T-cell persistence by immunophenotyping using flow cytometry in bone marrow, peripheral blood and CSF samples at multiple study time points following CAR T cell infusion

    Time frame: 1 month to 5 years

    Flow cytometry will be performed on bone marrow, peripheral blood and CSF samples at multiple study time points following CAR T cell infusion

Study contacts

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

Allen Yeoh, M.D

CONTACT

[email protected]

+65 6772 2002

Sponsors and collaborators

Lead sponsor

National University Hospital, Singapore

Other

Registry information

Official study title

Anti-CD7 Protein Expression Blocker (PEBL) Chimeric-Antigen Receptor (CAR) T-Cell Therapy for Relapsed/ Refractory T-Lineage Acute Lymphoblastic Leukaemia (CARTALL)

Important dates

Study start
2021
Primary completion
2026
Study completion
2026
First posted
Sep 14, 2021
Registry last updated
Sep 14, 2021

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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