Drug intelligence / Profile preview

durvalumab + lenalidomide + dexamethasone

Development stage
Discontinued
Lead developer
Bristol Myers Squibb
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous, Oral
01

Overview

This is an experimental **combination therapy** consisting of three agents: **durvalumab** (a monoclonal antibody that targets programmed death ligand 1, PD-L1), **lenalidomide** (an immunomodulatory and anti-neoplastic small molecule agent), and **dexamethasone** (a synthetic glucocorticoid corticosteroid). It has been studied in a Phase 1/2 clinical trial for the treatment of newly diagnosed multiple myeloma, particularly in transplant-ineligible and/or high-risk patients. The rationale stems from potential enhancement of anti-myeloma immune responses by combining immunomodulation (lenalidomide) with checkpoint inhibition (durvalumab) and corticosteroid-mediated anti-inflammatory/antitumor activity (dexamethasone). The main study (MEDI4736-MM-002) was placed on full clinical hold and terminated early by the FDA due to safety concerns extrapolated from similar combinations involving PD-1 inhibitors and immunomodulators in multiple myeloma[1][3][5][6][7].

Brand names
Imfinzi + Revlimid + dexamethasone
Other names
durvalumab + LEN + DEX
02

Targets

GR (Glucocorticoid receptor)CRBN (Cereblon)CD274 (Programmed cell death protein 1 ligand 1)

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