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Carfilzomib Lenalidomide Dexamethasone

European Myeloma Network B.V. · Phase 3 active Small molecule

This combination therapy kills multiple myeloma cells by inhibiting the proteasome (carfilzomib), modulating cereblon-mediated protein degradation (lenalidomide), and suppressing inflammatory cytokines (dexamethasone).

This combination therapy kills multiple myeloma cells by inhibiting the proteasome (carfilzomib), modulating cereblon-mediated protein degradation (lenalidomide), and suppressing inflammatory cytokines (dexamethasone). Used for Multiple myeloma (newly diagnosed and relapsed/refractory).

At a glance

Generic nameCarfilzomib Lenalidomide Dexamethasone
Also known asKRd
SponsorEuropean Myeloma Network B.V.
Drug classProteasome inhibitor + Immunomodulatory agent + Corticosteroid combination
Target20S proteasome (carfilzomib); Cereblon/E3 ubiquitin ligase (lenalidomide); Glucocorticoid receptor (dexamethasone)
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

Carfilzomib is a proteasome inhibitor that prevents degradation of pro-apoptotic proteins, triggering cancer cell death. Lenalidomide is an immunomodulatory drug that enhances T-cell proliferation and redirects cereblon E3 ligase to degrade oncogenic proteins. Dexamethasone is a corticosteroid that reduces inflammation and enhances the anti-myeloma effects of the other agents. Together, they target multiple pathways in myeloma cell survival and proliferation.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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