Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07100067

LCAR-F33S in Treatment of Relapsed/Refractory Multiple Myeloma

Led by Nanjing Legend Biotech Co. · Updated on 2025-12-29

35

Participants Needed

4

Research Sites

218 weeks

Total Duration

On this page

Sponsors

N

Nanjing Legend Biotech Co.

Lead Sponsor

I

Institute of Hematology & Blood Diseases Hospital, China

Collaborating Sponsor

AI-Summary

What this Trial Is About

A prospective, single-arm, open-label dose-exploration and expansion study to evaluate the safety, tolerability, pharmacokinetics, and antitumor efficacy characteristics of LCAR-F33S in patients with relapsed/refractory multiple myeloma(Investigator-initiated Study).

CONDITIONS

Official Title

LCAR-F33S in Treatment of Relapsed/Refractory Multiple Myeloma

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Voluntarily agree to participate in clinical research
  • Age 18 years or older
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2
  • Confirmed initial diagnosis of multiple myeloma according to IMWG criteria
  • Presence of measurable lesions
  • Previous treatment with one proteasome inhibitor, one immunomodulatory drug, and a CD38 monoclonal antibody
  • Received at least three prior lines of multiple myeloma therapy, each with at least one complete cycle, unless disease progression was documented
  • Expected survival of at least 3 months
  • Clinical laboratory values meeting screening criteria
Not Eligible

You will not qualify if you...

  • Prior therapy targeting FcRH5
  • Previous antineoplastic therapy meeting exclusion criteria before apheresis
  • Diagnosis of plasma cell leukemia, Waldenstrom macroglobulinemia, POEMS syndrome, or primary AL amyloidosis at screening
  • Positive test for HBsAg, HBV DNA, HCV antibody, HCV RNA, or HIV antibody
  • History of life-threatening allergic or hypersensitivity reactions to CAR-T cell products or their components including DMSO
  • Presence of serious underlying diseases
  • Females who are pregnant, breastfeeding, or planning pregnancy during or within one year after study treatment
  • Participation in other clinical studies

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

Beijing Boren Hospital

Beijing, China

Not Yet Recruiting

2

Institute of Hematology & Blood Diseases Hospital

Tianjin, China

Actively Recruiting

3

Institute of Hematology & Blood Diseases Hospital

Tianjin, China

Actively Recruiting

4

Wuhan Union Hospital

Wuhan, China

Actively Recruiting

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Research Team

T

Tingting Wang

CONTACT

J

Jianling Yao

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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