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Mezigdomide · BMS-986348, CC-92480

Small molecule (Molecular glue degrader) · Degrader of cereblon (CRBN) · developed by BRISTOL MYERS SQUIBB

Phase 3 Most advanced trial
BMY Developer
1 Registered trials

What is Mezigdomide?

Mezigdomide is a cereblon (CRBN) modulator that binds to CRBN and enhances the ubiquitin E3 ligase activity of the CRL4-CRBN complex, targeting substrate proteins for proteasomal degradation. This induces T-cell activation and downregulates proteins involved in cancer cell proliferation. It is studied in relapsed or refractory multiple myeloma.

Summary written with AI from the sources listed at the end of this page.

At a glance

Also known as
BMS-986348, CC-92480
Drug type
Small molecule (Molecular glue degrader)
Targets
cereblon (CRBN)
Mechanism
Degrader of cereblon (CRBN)
Pathways
proteasome-mediated degradation, T-cell activation
Therapy area
Oncology
Developer
BRISTOL MYERS SQUIBB (BMY)
FDA status
Investigational, not approved in the US. Most advanced trial: Phase 3
UNII
LA88IH4O02

🧪 Clinical trials

TrialPhaseConditionStatusSponsor
NCT05552976 Phase 3 Relapsed or Refractory Multiple Myeloma Active not recruiting BMY

Trials of the companies BioRadar tracks, from ClinicalTrials.gov, most advanced phase first.

Conditions studied

Relapsed or Refractory Multiple Myeloma

Other drugs acting on CRBN

More from BRISTOL MYERS SQUIBB

Sources

Updated Oct 3, 2026. Something wrong or missing? Report it on the BMY page.

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Data: FDA (Drugs@FDA, Purple Book, DailyMed), NIH (NCI Thesaurus, GSRS, RxNorm), ClinicalTrials.gov • Informational purposes only, not medical or investment advice. • All drugs A–Z

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