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A Study to Evaluate the Safety, Effectiveness and Tolerable Dose of Arlocabtagene Autoleucel (BMS-986393) in Novel Combinations in Participants With Relapsed and/or Refractory Multiple Myeloma

RecruitingPhase 1

A Phase 1, Multicenter, Open-label Study to Evaluate the Safety and Preliminary Efficacy of Arlocabtagene Autoleucel (BMS-986393) in Novel Combinations in Participants With Relapsed and/or Refractory Multiple Myeloma and Determine the Recommended Dose for Each Add-on Investigational Component

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* History of relapsed and/or refractory multiple myeloma (RRMM) treated with at least 3 (Part 1), history of RRMM or at least 1 but not greater than 3 prior anti-myeloma treatment (PAMT) regimens (Part 2, Arms A, B, C, and D); history of quadruple class exposed RRMM having received BCMA TCE as the most recent line of therapy (Part 2, Arm E).
* Measurable multiple myeloma (MM) as per International Myeloma Working Group (IMWG).
* Eastern Cooperative Oncology Group performance status of 0-1.
* Adherence to contraception requirements.

Exclusion Criteria:

* Prior treatment with alnuctamab (Arm A), mezigdomide (Arms B and E), iberdomide (Arm C), elranatamab (Arm D) or BCMA-targeting therapy (Part 2 Arms A and D).
* Prior treatment with GPRC5D-targeting therapies as of Protocol Amendment 02 (Part 1 and Part 2).
* Other protocol-defined inclusion/exclusion criteria apply.

About the study

The purpose of this study is to establish a safe and tolerable dose of arlocabtagene autoleucel (BMS-986393) in combinations with alnuctamab, mezigdomide, iberdomide, and elranatamab in participants with relapsed and/or refractory multiple myeloma (RRMM).

What is being tested

Sponsor: Juno Therapeutics, Inc., a Bristol-Myers Squibb Company · Participants: 187 · Started: Feb 22, 2024

Contact the study team

Official record on ClinicalTrials.gov — NCT06121843

Locations in the U.S.

AlabamaUniversity of Alabama at Birmingham, Birmingham
ArizonaMayo Clinic in Arizona - Phoenix, Phoenix
CaliforniaCity of Hope Comprehensive Cancer Center, Duarte
FloridaMayo Clinic in Florida, Jacksonville
GeorgiaNorthside Hospital, Atlanta
MassachusettsBeth Israel Deaconess Medical Center, Boston
Dana-Farber Cancer Institute, Boston
MinnesotaMayo Clinic in Rochester, Minnesota, Rochester
NebraskaUniversity Of Nebraska Medical Center, Omaha
New JerseyJohn Theurer Cancer Center at Hackensack University Medical Center, Hackensack
New YorkRoswell Park Cancer Institute, Buffalo
Laura and Isaac Perlmutter Cancer Center, New York
Memorial Sloan Kettering Cancer Center, New York
TennesseeTennessee Oncology, Nashville
TexasUniversity of Texas MD Anderson Cancer Center, Houston

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.