Study of BMS-986393 a GPRC5D-directed CAR T Cell Therapy in Adult Participants With Relapsed or Refractory Multiple Myeloma

ID#: NCT06297226

Age: 18 years - 66+

Gender: All

Healthy Subjects: No

Study Phase: Phase 2

Recruitment Status: Recruiting

Start Date: March 21, 2024

End Date: June 04, 2030

Contact Information:
BMS Clinical Trials Contact Center www.BMSClinicalTrials.com
855-907-3286
First line of the email MUST contain NCT # and Site #.
Summary: The purpose of this study is to evaluate the effectiveness and safety of BMS-986393 in participants with relapsed or refractory multiple myeloma.
Eligibility: Inclusion Criteria

- Documented diagnosis of multiple Mmyeloma (MM) as per International Myeloma Working Group (IMWG) criteria.

- Received at least 4 classes of MM treatment [including immunomodulatory drug (IMiD), proteasome inhibitor (PI), anti CD38 mAb, and anti-B cell maturation antigen (BCMA) therapy], and at least 3 prior lines of therapy (LOT).

- Documented disease progression during or after their last anti-myeloma regimen as per IMWG.

- Participants must have measurable disease during screening.

- Have measurable disease during screening.

- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1. Exclusion Criteria

- Active or history of central nervous system involvement with MM.

- Active systemic fungal, bacterial, viral, or other infection despite appropriate anti-infective treatment at the time of leukapheresis.

- Received any prior therapy directed at G protein-coupled receptor class C, group 5, member D (GPRC5D) or has received other prior treatment for MM without the required washout prior to leukapheresis.

- Other protocol-defined Inclusion/Exclusion criteria apply.