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Study identifier: NCT05519085 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Study to Evaluate Mezigdomide, Bortezomib and Dexamethasone (MEZIVd) Versus Pomalidomide, Bortezomib and Dexamethasone (PVd) in Participants With Relapsed or Refractory Multiple Myeloma (RRMM)

Condition: Relapsed or Refractory Multiple Myeloma  ·  Sponsor: Celgene

PhasePhase 3
Planned participants810
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to compare the efficacy and safety of mezigdomide (CC-92480), bortezomib and dexamethasone (MeziVd) versus pomalidomide, bortezomib and dexamethasone (PVd) in participants with relapsed or refractory multiple myeloma (RRMM) who received between 1 to 3 prior lines of therapy and who have had prior lenalidomide exposure.

This description comes directly from the study's public registry record.

Talk to the study team

BMS Clinical Trials Contact Center www.BMSClinicalTrials.com  ·  855-907-3286  ·  Clinical.Trials@bms.com

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Locations (266)

Local Institution - 0366Los Alamitos, California, United StatesActive Not Recruiting
Local Institution - 0272San Diego, California, United StatesCompleted
Local Institution - 0273West Hollywood, California, United StatesCompleted
Local Institution - 0381Aurora, Colorado, United StatesNot Yet Recruiting
Local Institution - 0380Farmington, Connecticut, United StatesCompleted
Local Institution - 0208New Haven, Connecticut, United StatesWithdrawn
Local Institution - 0303Coral Springs, Florida, United StatesActive Not Recruiting
Local Institution - 0403Fort Myers, Florida, United StatesActive Not Recruiting
Local Institution - 0401St. Petersburg, Florida, United StatesActive Not Recruiting
Local Institution - 0402West Palm Beach, Florida, United StatesActive Not Recruiting
Local Institution - 0211Athens, Georgia, United StatesActive Not Recruiting
Local Institution - 0048Marietta, Georgia, United StatesWithdrawn

+ 254 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05519085