Drug intelligence / Profile preview

mezigdomide + carfilzomib + dexamethasone

Development stage
Phase 3
Lead developer
Bristol Myers Squibb
Modality
Small Molecules
Administration
Oral (mezigdomide), Intravenous (carfilzomib), Oral (dexamethasone), Intravenous (dexamethasone, Optionally)
01

Overview

Mezigdomide + carfilzomib + dexamethasone is an investigational, three-drug combination for the treatment of relapsed or refractory multiple myeloma. **Mezigdomide** is an oral cereblon E3 ligase modulator (CELMoD) that induces maximal degradation of Ikaros and Aiolos transcription factors, leading to increased apoptosis of multiple myeloma cells and immune-stimulatory effects. **Carfilzomib** is a selective proteasome inhibitor that induces apoptosis by blocking protein degradation in cancer cells, and **dexamethasone** is a synthetic glucocorticoid corticosteroid that reduces inflammation and enhances cancer cell death. This combination (referred to as MeziKd) is under investigation in multiple phase 1/2 and phase 3 clinical trials. It is designed for patients with multiple myeloma who are refractory or have relapsed after prior therapies, including lenalidomide and anti-CD38 monoclonal antibodies[1][2][4][5][7].

Brand names
MeziKd
Other names
mezigdomide + carfilzomib + dexamethasoneMeziKD
02

Targets

PSMB6 (Proteasome 20S subunit beta 6)PSMB7 (Proteasome subunit beta type-7)PSMB5 (Proteasome subunit beta Type-5)CRBN (Cereblon)GR (Glucocorticoid receptor)IKZF3 (Zinc finger protein Aiolos)IKZF1 (Ikaros family zinc finger protein 1)

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