GPRC5D-directed CAR T Cell Therapy in Participants with Relapsed or Refractory Multiple Myeloma

Overview

About this study

The purpose of this study is to evaluate the efficacy of BMS-986393 in participants with quadruple class exposed R/R MM having received at least 4 prior LOT.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Participants aged ≥ 18 years of age or majority, inclusive, with documented diagnosis of MM as per International Myeloma Working Group (IMWG) criteria.
  • Participant must have received at least 4 classes of MM treatment (including an IMiD, PI, anti-CD38 mAb, and anti-BCMA therapy), and at least 3 prior LOT.
  • Participants must have documented disease progression during or after their last anti-myeloma regimen (as per IMWG).
  • Participants must have measurable disease during screening.
  • Participant must have Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
  • Adherence to contraception requirements.

Exclusion Criteria: 

  • Participant with known active or history of central nervous system involvement with MM.
  • Participant has active systemic fungal, bacterial, viral, or other infection despite appropriate anti-infective treatment at the time of leukapheresis.
  • Participant has received any prior therapy directed at GPRC5D or has received other prior treatment for MM without the required washout prior to leukapheresis.
  • Participant has inadequate organ function (per protocol definition).

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 2/27/2024. Questions regarding updates should be directed to the study team contact.

 

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Taxiarchis Kourelis, M.D.

Contact us for the latest status

Contact information:

Cancer Center Clinical Trials Referral Office

(855) 776-0015

Jacksonville, Fla.

Mayo Clinic principal investigator

Vivek Roy, M.D.

Contact us for the latest status

Contact information:

Cancer Center Clinical Trials Referral Office

(855) 776-0015

More information

Publications

Publications are currently not available
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CLS-20582089

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