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Recruiting Phase 1/2

CD7 CAR-T Bridging to alloHSCT for R/R CD7+Malignant Hematologic Diseases

NCT05827835 · tracked via the Priya Life Science China tracker
Phase
Phase 1/2
Started
2023-04-30
Last updated
2025-08-13

Condition(s) studied

Hematologic DiseasesNeoplasms

Investigational drug(s) / intervention(s)

CD7 CAR-T cells injectionAllogeneic hematopoietic stem cell transplantation

CD7 CAR-T cells injection: CD7 CAR T cells treat patients with refractory or relapsed CD7 positive Malignant Hematologic Diseases

Allogeneic hematopoietic stem cell transplantation: In this study, Allogeneic hematopoietic stem cell transplantation is used as a bridge therapy to CD7 CAR T cells infusion to treat patients with refractory or relapsed CD7 positive Malignant Hematologic Diseases

Study summary

This is a single-arm, open-label, single-center, phase I/II study. The primary objective is to evaluate the safety of CD7 CAR-T Bridging to allo-HSCT therapy for patients with CD7-positive relapsed or refractory Malignant Hematologic Diseases

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Provision of signed and dated informed consent form (ICF) * Male or female, older than 18 years (including 18 years) * Anticipated survival time more than 12 weeks * Eastern Cooperative Oncology Group (ECOG) performance status ≤2 * According to the National Comprehensive Cancer Network (NCCN) Clinical Practice Guidelines for Acute Lymphocytic Leukemia and Acute Myeloid Leukemia (2016. v1), patients diagnosed as CD7+ALL and AML * Consistent with r/r CD7+acute leukemia diagnosis, including any of the following conditions * a. No CR after standard chemotherapy * b. The first induction reaches CR, but CR ≤ 12 months * c. Patients with r/r CD7+acute leukemia have not responded to the first or multiple remedial treatments * d. Multiple recurrences * Philadelphia chromosome negative (Ph -) subjects; Or cannot tolerate tyrosine kinase inhibitor (TKI) treatment; Or Philadelphia chromosome positive (Ph+) subjects who did not respond to both TKI treatments * Normal lung function, oxygen saturation greater than 92% without oxygen inhalation * The blood biochemical test results are consistent with the following results * a. (AST) and (ALT) ≤ 2.5 × (ULN) * b. Total bilirubin ≤ 1.5 × ULN * c. 24-hour serum creatinine clearance ≥ 30 mL/min * d. Lipase and amylase ≤ 2 × ULN * Fertility capable men and women of childbearing age must agree to use effective contraception starting with the signing of an informed consent form until within 2 years after the use of the study drug. Women of reproductive age include pre menopausal women and women within 2 years after menopause. The blood pregnancy test for women of reproductive age must be negative at screening Exclusion Criteria: * Patients with the history of epilepsy or other CNS disease * Pregnant or breastfeeding * Active infection with no cure * Patients with prolonged QT interval time or severe heart disease * Have experienced hypersensitivity or intolerance to any drug used in this study * Patients who received anticancer chemotherapy or other drug treatment within 2 weeks before screening * Previous malignant tumors that require treatment or have evidence of recurrence within the previous 5 years of screening * Clinically significant central nervous system lesions such as seizures, cerebral vascular ischemia/hemorrhage, dementia, cerebellar disease, psychosis, active central nervous system involvement, or cancerous meningitis * In the past 2 years, terminal organ damage caused by autoimmune diseases (such as Crohn's disease, rheumatoid arthritis, systemic lupus erythematosus) or the need for systematic application of immunosuppressive or other systemic disease control drugs * Severe active viral, bacterial, or uncontrolled systemic fungal infections; Genetic bleeding/coagulation disorders, a history of non-traumatic bleeding or thromboembolism, and other diseases that may increase the risk of bleeding * Patients who received autologous hematopoietic stem cell transplantation (ASCT) within 8 weeks before screening, or who plan to undergo ASCT during this study * Participated in clinical trials of other drugs within 4 weeks or 5 drug half-lives (T1/2) before screening * Any situation that the researchers believe may increase the risk of patients or interfere with the test results.

Primary outcome measure(s)

  • Incidence and level of AE and SAE — Baseline up to 28 days after CD7 CAR T-cells infusion
    Adverse events assessed according to NCI-CTCAE v5.0 criteria

Trial sites (1)

FacilityCityRegionStatus
The first affiliated hospital of medical college of zhejiang university Hangzhou Zhejiang Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05827835 on ClinicalTrials.gov ↗ ← All trials in China