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Status unknownNCT05325801Updated Apr 13, 2022

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

A Phase 1 interventional study of BMCA and GPRC5D dual target CAR-T cells(OriC321) in Multiple Myeloma, sponsored by Zhejiang University. Status unknown. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2022-04-13.

Sponsored by Zhejiang University · Phase 1, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Apr 2022), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Phase 1
Study type
Interventional
Enrollment
9
Allocation
Not applicable
Ages
18 Years to 75 Years
Sex
All
01

Study summary

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

02

Conditions studied

03

In context

Multiple Myeloma

3,632 studies on the registry are indexed under Multiple Myeloma; 745 are open to participants now.

This study's planned enrollment of 9 is below the median of 41 across 2,907 interventional studies indexed under Multiple Myeloma.

Browse Multiple Myeloma studies →

Lead sponsor

Zhejiang University is the lead sponsor of 351 studies on the registry; 165 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

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.
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
9 participants (estimated)

Study arms

  • Experimental
    BMCA and GPRC5D dual target CAR-T cells (OriC321)

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

Interventions

  • BiologicalBMCA and GPRC5D dual target CAR-T cells(OriC321)

    Patients will receive lymphodepleting chemotherapy followed by a single infusion of OriC321

06

What researchers measure

Primary outcomes

  1. Incidence, severity AEs/SAEs

    Time frame: 2 years after CAR-T cell infusion

Secondary outcomes

  1. Concentration of CAR-T cells

    Time frame: 2 years after CAR-T cell infusion

  2. Objective response rate (ORR)

    Time frame: 2 years after CAR-T cell infusion

  3. Progression-free survival (PFS)

    Time frame: 2 years after CAR-T cell infusion

  4. Duration of response (DOR)

    Time frame: 2 years after CAR-T cell infusion

  5. Overall survival (OS)

    Time frame: 2 years after CAR-T cell infusion

  6. Percentage of Patients With Negative Minimal Residual Disease (MRD)

    Time frame: 2 years after CAR-T cell infusion

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 13, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05325801
Lead sponsor
Zhejiang University
Responsible party
He Huang (Prof., Zhejiang University) — Principal investigator
First posted
Apr 13, 2022
Start date
Apr 2022 (estimated)
Primary completion
Mar 2024 (estimated)
Completion
Mar 2025 (estimated)
Last update
Apr 13, 2022

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Apr 2022. You cannot join it, but the record below documents what was studied.

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