LCAR-F33S in Treatment of Relapsed/Refractory Multiple Myeloma

Legend Biotech

Status

Enrolling

Conditions

Relapsed/Refractory Multiple Myeloma(MM)

Treatments

Biological: LCAR- F33S cells intravenous infusion

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT07100067

LB2502-0001

Details and patient eligibility

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).

Full description

This study is a prospective, single-arm, open-label clinical study to evaluate the safety, tolerability, pharmacokinetics, and antitumor efficacy characteristics of LCAR-F33S in patients with relapsed/refractory multiple myeloma. All subjects who meet the eligibility criteria will receive intravenous injection of LCAR-F33S cell injection. The study will include the following sequential phases: screening, apheresis, pre-treatment (lymphodepleting chemotherapy), treatment, and follow-up.

Enrollment

35 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Subjects voluntarily participate in clinical research.
Age ≥18 years old.
Eastern Cooperative Oncology Group (ECOG) score 0-2.
Examination evidence of initial diagnosis of MM according to IMWG diagnostic criteria.
Measurable lesions were present.
Subjects have received treatment with one PI, one IMiD and a CD38 monoclonal antibody.
Subjects have received at least three previous lines of multiple myeloma therapy, each with at least one complete therapy cycle, unless the best response to the therapeutic regimen was documented as disease progression (PD confirmed according to IMWG criteria).
Expected survival ≥3 months.
Clinical laboratory values in the screening period meet criteria.

Exclusion criteria

Received previous therapy targeting FcRH5 targets.
Prior antineoplastic therapy and meet exclusion criteria (before apheresis);
Subjects had Plasma cell leukemia, Waldenstrom macroglobulinemia, POEMS syndrome, or primary AL amyloidosis at the time of screening.
Subjects who were positive for any of HBsAg, HBV DNA, HCV-Ab, HCV RNA, and HIV-Ab;
Life-threatening allergic reactions, hypersensitivity reactions, or intolerance to CAR-T cell formulations or their excipients, including DMSO, are known.
Serious underlying diseases were present.
Female subjects who were pregnant, breastfeeding, or planning to become pregnant while participating in this study or within 1 year of receiving study treatment.
Also enrolled in other clinical studies.