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

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

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。

Eligibility
Participation Requirements
Sex: All
Minimum Age: 3
Maximum Age: 70
Healthy Volunteers: f
View:

• 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.

Locations
Other Locations
China
Union Hospital
RECRUITING
Wuhan
Contact Information
Primary
Heng Mei, Ph.D&M.D
hmei@hust.edu.cn
027-8572600
Backup
Yinqiang Zhang
zhang_yq@hust.edu.cn
15007101371
Time Frame
Start Date: 2024-10-31
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 10
Treatments
Experimental: RD13-02 cell infusion
RD13-02 cells targeting CD7 were injected intravenously
Related Therapeutic Areas
Sponsors
Leads: Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Collaborators: Nanjing Bioheng Biotech Co., Ltd.

This content was sourced from clinicaltrials.gov