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NCT Number: NCT06732492

RD13-02 Cell Injection in Patients with Relapsed or Refractory CD7-Positive Natural Killer/T Cell Malignancies

This is a single-arm, open-label, single-center, phase I study. The primary objective is to evaluate the safety of CD7 Chimeric Antigen Receptor-T(CAR-T) therapy for patients with CD7-positive relapsed or refractory natural killer/T cell lymphoma, and to evaluate the pharmacokinetics of CD7 CAR-T in patients。

Recruiting

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Key information

Age range

3 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age 3-70
  • Diagnosis of r/r NK/T lymphoma.
  • CD7 positive expression
  • Bone marrow lymphoblasts ≥5% by morphologic evaluation at screening
  • Creatinine clearance (as estimated by Cockcroft Gault) ≥ 60 mL/min, Serum alanine aminotransferase(ALT)/aspartate aminotransferase(AST) < 3×upper limit of normal, Total bilirubin < 1.5×upper limit of normal or ≤1.5mg/dl
  • Left ventricular ejection fraction ≥ 50% .
  • Baseline oxygen saturation ≥ 92% on room air.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2.
  • The estimated survival time is more than 3 months.
  • Subjects or their legal guardians volunteer to participate in the study and sign the informed consent.

Exclusion criteria

  • Subjects with concomitant genetic syndromes associated with bone marrow failure states.
  • Isolated extramedullary lesions
  • Subjects with some cardiac conditions will be excluded.
  • With uncontrolled active central nervous system leukemia (CNSL), cerebrospinal fluid grade Central Nervous System3(CNS3).
  • History of traumatic brain injury, consciousness disturbance, epilepsy, cerebrovascular ischemia, and cerebrovascular hemorrhagic disease, which might compromise the ability of the subject to compliance with the obligations under the protocol.
  • History of malignancy other than non-melanoma skin cancer or carcinoma.
  • Primary immune deficiency.
  • Presence of uncontrolled infections.
  • Subjects with some anticancer therapy before CAR-T infusion will be excluded.
  • Active uncontrolled acute infections.
  • Known history of infection with human immunodeficiency virus (HIV); active or latent hepatitis B, hepatitis C and syphilis.
  • Subjects who are receiving systemic steroid therapy prior to screening.

Treatment and study plan

RD13-02 cell infusion

Drug

CAR-T cells

Other names: universal CD7 CAR-T cells

Primary outcomes

  1. Overall response rate (ORR)

    Time frame: Evaluate at 4 weeks after CAR-T infusion

    The proportion of patients with complete response (CR) /complete response with incomplete blood cell recovery (CRi)

Secondary outcomes

  1. Duration of remission (DOR)

    Time frame: Up to 1 years after CAR-T infusion

    The time from CR/CRi and PR to disease relapsed or death due to disease progression after CAR-T infusion

  2. Event-free survival (EFS)

    Time frame: Up to 1 years after CAR-T infusion

    The time from first achieving CR/CRi to relapse or death

  3. Overall survival (OS)

    Time frame: Up to 1 years after CAR-T infusion

    The time from CAR-T infusion to death due to any cause

Study contacts

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

Heng Mei, Ph.D&M.D

CONTACT

[email protected]

027-8572600

Yinqiang Zhang

CONTACT

[email protected]

15007101371

Sponsors and collaborators

Lead sponsor

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

Other

Collaborators

  • Nanjing Bioheng Biotech Co., Ltd.

Registry information

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Dec 13, 2024
Registry last updated
Dec 13, 2024

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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