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

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorCelgene

About this trial

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.

Eligibility criteria

Qualifiers

Participants received 1 to 3 prior lines of antimyeloma therapy.

Participants achieved minimal response [MR] or better to at least 1 prior antimyeloma therapy.

Disqualifiers

For participants with prior treatment of a bortezomib containing regimen, the best response achieved was not a minimal response (MR) or better, or participant discontinued bortezomib due to toxicity.

Participant has had prior treatment with mezigdomide or pomalidomide.

Other protocol-defined Inclusion/Exclusion criteria apply.

Trial design

Treatments tested in this trial

  • mezigdomide
  • Pomalidomide
  • Bortezomib
  • Dexamethasone

Treatment groups

810 Participants
are divided into 2 treatment groups

Sponsors and collaborators