Mezigdomide

Drug

Also known as: CC-92480

Drug Profile

Mezigdomide is a CELMoD agent in development for multiple myeloma, including relapsed or refractory disease settings. Its program includes Phase 3 SUCCESSOR trials in combination regimens. It is not FDA approved.

Drug Class
CELMoD (Cereblon E3 Ligase Modulator)
Approval Status
Not FDA approved.
Mechanism of Action
Potently degrades Ikaros and Aiolos transcription factors, inhibiting myeloma cell growth.
Indications
  • \Multiple myeloma (including relapsed/refractory multiple myeloma in development)\

Related News

Related Clinical Trials

NCT ID Title Status Phase
NCT07356154

A Study of Revumenib and Mezigdomide in People With Leukemia

RECRUITING PHASE1/PHASE2
NCT07355335

Ziftomenib + Mezigdomide in Adolesc. and Adults w/ R/R AML

NOT_YET_RECRUITING PHASE1
NCT07105059

A Study of Teclistamab and Mezigdomide in People With Multiple Myeloma

RECRUITING PHASE1
NCT07032714

Mezigdomide and Talquetamab in Relapsed and Refractory Multiple Myeloma

RECRUITING PHASE1
NCT06994117

Expanded Access for Mezigdomide

AVAILABLE
NCT06988488

A Study to Determine the Recommended Dose and Schedule, and Evaluate the Safety and Preliminary Efficacy of Mezigdomide in Combination With Elranatamab in Participants With Relapsed and/or Refractory Multiple Myeloma

RECRUITING PHASE1/PHASE2
NCT06645678

Mezigdomide and Elranatamab for Relapsed and/or Refractory Multiple Myeloma

RECRUITING PHASE1/PHASE2
NCT06627751

Mezigdomide, Carfilzomib, and Dexamethasone for the Treatment of Relapsed or Refractory Multiple Myeloma in Patients With Extramedullary Disease

RECRUITING PHASE2
NCT06318676

A Study to Evaluate the Drug Levels of Mezigdomide in Adult Participants With Renal Impairment

COMPLETED PHASE1
NCT06163898

A Study to Evaluate Alnuctamab in Combination With Mezigdomide in Participants With Relapsed and/or Refractory Multiple Myeloma

TERMINATED PHASE1