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A Study to Evaluate Mezigdomide in Combination With Carfilzomib and Dexamethasone (MeziKD) Versus Carfilzomib and Dexamethasone (Kd) in Participants With Relapsed or Refractory Multiple Myeloma (SUCCESSOR-2)

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NCT05552976

Sponsored by Bristol-Myers Squibb (industry) · BMY — their whole pipeline →.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
606actual
Sites
207
Countries
Argentina, Australia, Austria +24

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-01-10actualWhen the study began enrolling
Primary completion2026-07-18estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2029-07-25estimatedThe whole study's end, after follow-up
First posted2022-09-23actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-04-01actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Relapsed or Refractory Multiple Myeloma

Interventions

  • Drug: Mezigdomide — also filed as BMS-986348, CC-92480
  • Drug: Carfilzomib — also filed as Kyprolis
  • Drug: Dexamethasone — also filed as Decadron, Dex

Primary outcome

what the primary-completion date above is the date OF
Progression-free Survival (PFS)
measured Up to approximately 5 years

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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