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Chimeric antigen receptor engineered T cells for treating malignant cancers

Safety and efficacy of chimeric antigen receptor engineered T cells for treating malignant cancers

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000032124
Enrollment
Unknown
Registered
2020-04-20
Start date
2020-04-13
Completion date
Unknown
Last updated
2020-04-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

B cell leukemia and lymhpoma, multiple myeloma, and ovarian cancer

Interventions

5 groups:CART therapy

Sponsors

The Second Xiangya Hospital of Central South University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Voluntary to enroll with signed consent form; 2. Aged 18 to 65 years, the expected survival time is more than 3 months; 3. ECOG score =3.0x10^9/L, Lymphocyte count >0.5x10^9/L, PLT >=50x10^9/L (not including patients with leukemia and lymphoma); liver function: TBIL =55% 6. Female patient within childbearing age must use appropriate contraception during the study, and urea/blood pregnancy test must be negative before and during the study.

Exclusion criteria

Exclusion criteria: 1. Treated with CART therapy previously; 2. Pregnant or nursing female patients; 3. Remaining disease of other malignant tumors; 4. Patients with severe psychiatric disorders; 5. Patients with other serious diseases (such as autoimmune diseases, immune deficiency, organ transplantation) that conflict with this study; 6. Patients with allogeneic hematopoietic stem cell transplantation; 7. Patients with infectious or viral diseases (HIV positive, syphilis, hepatitis b or c, etc.); 8. Patients with severe allergic constitution; 9. Patients with severe heart, liver, renal insufficiency, diabetes and other diseases; 10. Patients who have participated in other clinical studies in the past 3 months or have previously received other gene product treatments.

Design outcomes

Primary

MeasureTime frame
Partial or complete remission;

Countries

China

Contacts

Public ContactGuangshi Tao

The Second Xiangya Hospital of Central South University

taoguangshi@csu.edu.cn+86 13574850167

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026