BCMA-targeted LCAR-BCDR Cells in Patients With Relapsed/Refractory Multiple Myeloma

NCT05376345 · Status: TERMINATED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2026-08-11

No results posted yet for this study

Summary

This is a prospective, single-arm, open-label, dose-finding and dose-expansion study that evaluates the safety, tolerability, PK, and anti-tumor efficacy of LCAR-BCDR cell preparations in relapsed/refractory multiple myeloma subjects who received adequate standard therapy.

Conditions

Interventions

BIOLOGICAL

LCAR-BCDR cells product

Before treatment with LCAR-BCDR cells, subjects will receive a conditioning regimen

Sponsors & Collaborators

  • Nanjing Legend Biotech Co.

    collaborator INDUSTRY
  • First Affiliated Hospital of Wenzhou Medical University

    collaborator OTHER
  • Beijing Boren Hospital

    collaborator OTHER
  • Zhejiang Provincial People's Hospital

    collaborator OTHER
  • Shanghai Fourth People's Hospital Tongji University

    collaborator OTHER
  • Institute of Hematology & Blood Diseases Hospital, China

    collaborator OTHER
  • Shanghai Changzheng Hospital

    lead OTHER

Principal Investigators

  • Weijun Fu, PhD · Shanghai Changzheng Hospital

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-09-01
Primary Completion
2025-05-27
Completion
2025-05-27

Countries

  • China

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05376345 on ClinicalTrials.gov