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BCMA-CAR-T in Relapsed/Refractory Multiple Myeloma

H

Henan Cancer Hospital

Status and phase

Unknown
Phase 1

Conditions

Relapsed/Refractory Myeloma

Treatments

Drug: BCMA nanobody CAR-T cells

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT03664661
HenanCH CAR 2-2

Details and patient eligibility

About

Evaluation of the safety and efficacy of BCMA nanobody CAR-T cells in relapsed/refractory myeloma

Full description

There are no effective regimens for relapsed/refractory myeloma. BCMA express extensively in mature B cells and plasma cells. Myeloma cells express BCMA universally. BCMA signal pathway can induce plasma cell proliferation and survival, down-regulation of BCMA could control the progression of myeloma. The BCMA CAR used in this study consists of BCMA nanobody, CD8 hinge, transmembrane region and 4-1bb co-stimulation domain.

Enrollment

15 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 and ≤70 years old and the expected lifetime >3 months

    • Active myeloma according to IMWG criteria, and BCMA positive by immunohistochemistry or flow cytometry
    • No effective treatment option available
    • ECOG score 0-2
    • Sufficient heart, liver, kidney function (heart: no heart disease or coronary heart disease, patient heart function NYHA grade 1-2; liver: TBIL ≤ 3ULN, AST ≤ 2.5ULN, ALT ≤ 2.5ULN; kidney: Cr≤ 1.25ULN);
    • smoothly peripheral superficial veins
    • No other serious diseases that conflict with this protocol (eg, autoimmune diseases, immunodeficiency, organ transplantation)
    • No history of other malignancies
    • Women of childbearing age must be negative for blood pregnancy test within 7 days and must take appropriated contraceptive measures during and 3 months after the study
    • The patient himself agrees to participate in this clinical study and signed the "informed consent"

Exclusion criteria

  • Severe infectious 4 weeks before enrollment
  • Active hepatitis B or C viral hepatitis, HIV,
  • Severe autoimmune disease or immunodeficiency disease
  • Severe allergies
  • Severe mental disorder
  • Patients who used high-dose glucocorticoids within 1 week
  • Participation in other clinical studies in the past 3 months or having been treated with other gene products

Trial design

15 participants in 1 patient group

experimental group
Experimental group
Description:
BCMA nanobody CAR-T cells
Treatment:
Drug: BCMA nanobody CAR-T cells

Trial contacts and locations

1

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Central trial contact

Yongping Song, M.D; Quanli Gao, M.D

Data sourced from clinicaltrials.gov

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