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A Study of CAR-T Cells Targeting Both BCMA and GPRC5D in Treatment of Relapsed or Refractory Multiple Myeloma

Zhejiang University logo

Zhejiang University

Status and phase

Not yet enrolling
Phase 1

Conditions

Multiple Myeloma

Treatments

Biological: BMCA and GPRC5D dual target CAR-T cells(OriC321)

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

An Open-Label, Dose Finding Study to Investigate the Safety, Pharmacokinetics, and Preliminary Efficacy of BMCA and GPRC5D dual target CAR-T cells therapy in Patients with relapsed or refractory multiple myeloma

Enrollment

9 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Signed and dated, written informed consent prior to any study specific procedures;

  • Estimated life expectancy of minimum of 12 weeks;

  • ECOG 0-2;

  • Diagnosed as multiple myeloma according to the IMWG criteria;

  • Evidence of cell membrane GPRC5D and/or BCMA expression, as determined by a validated immunohistochemistry (IHC) or flow cytometry of tumor tissue; Subjects should have measurable disease. At least meet one of the following criteria:

    1. If IgG type MM, serum M protein ≥10g/L; if IgA, IgD, IgE or IgM type MM, serum M protein ≥5g/L;
    2. urine M protein level ≥0.2g(200mg/24h);
    3. light chain type MM, serum free light chain (sFLC) ≥ 100mg / L and K/ λ FLC ratio is abnormal;
    4. there are extramedullary lesions;
  • Subjects have had at least 3 prior lines of therapy including chemotherapy based on proteasome inhibitors (PIs) and immunomodulatory agents (IMiDs);

  • Adequate organ functions

Exclusion criteria

  • Active smoldering multiple myeloma;
  • Active plasma cell leukemia;
  • With organ amyloidosis;
  • Central nervous system (CNS) involvement;
  • Pregnant or breastfeeding;
  • Hepatitis B virus (HBV) surface antigen (HBsAg) or hepatitis B core antibody-positive and detectable HBV DNA in peripheral blood; Hepatitis C virus (HCV) antibody and hepatitis C virus RNA in peripheral blood; Human immunodeficiency virus (HIV) antibody
  • Uncontrolled Hypertension hypertension defined as a blood pressure (BP) ≥150/95 mmHg; Symptomatic heart failure per New York Heart Association Classification Class II, III or IV), Mean resting corrected QT interval corrected by Fridericia's formula (QTcF) > 470 msec (female), 450 msec (male) obtained from ECG; Baseline left ventricular ejection fraction (LVEF) below institution's lower limit of normal (LLN) or <50%;
  • Have a history of another primary malignancy within 5 years prior to starting study treatment. Exceptions here are as follows: the disease under study; adequately treated basal or squamous cell carcinoma of the skin; cancer of the cervix in situ.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

9 participants in 1 patient group

BMCA and GPRC5D dual target CAR-T cells (OriC321)
Experimental group
Treatment:
Biological: BMCA and GPRC5D dual target CAR-T cells(OriC321)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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