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항목
AntibodyCurated CoreFDAstaleApproved
daratumumab (Darzalex)
Janssen·CD38
454 trials
ADCCurated CoreFDAstaleApproved
belantamab mafodotin (Blenrep, GSK2857916)
GSK·BCMA
78 trials
Overview
Program
Darzalex (daratumumab)Blenrep (belantamab mafodotin)
Overview
Company
JanssenGSK
Overview
Modality
ANTIBODYADC
Overview
Target
CD38BCMA
Overview
Indication
Multiple myelomaMultiple myeloma
Overview
Phase
APPROVEDAPPROVED
Overview
Status
APPROVEDDISCONTINUED
Overview
Content status
Curated CoreCurated Core
Overview
Data Confidence
Editorial scope · Curated CoreEditorial scope · Curated Core
Overview
Development Signal
Development Signal · EstablishedDevelopment Signal · Established
Overview
Approval status
FDA approvedFDA approved
Positioning
Key differentiator
Direct on-tumor + immunomodulatory effectsBCMA-targeted ADC with ocular AEs
Positioning
Known limitation
CD38 downregulation, high tumor burden, and impaired effector function after prior lines.bypass this immune effector cell dependence, we developed a novel strategy using antibody-drug conjugates (ADCs)
Technology
Payload
—MMAF
Technology
Linker
—Non-cleavable
MoA
Mechanism
Daratumumab binds CD38 on plasma cells and other immune cells, inducing direct apoptosis, Fc-mediated ADCC/CDC, and immunomodulatory effects including depletion of CD38+ regulatory cells and enhanced T-cell clonality.Belantamab mafodotin binds BCMA on plasma cells; afucosylated Fc enhances immune engagement while MMAF (microtubule inhibitor) payload is internalized and causes cell death.
MoA
Biomarker
CD38 expression on clonal plasma cells (universal in MM).BCMA expression on myeloma cells.
Toxicology
Species
Cynomolgus monkeyMouse, Rat
Toxicology
Animal (cat.)
NHPHuman
Toxicology
Major finding
Infusion-related reactions (premedication required), cytopenias, and increased infection risk; subcutaneous formulation reduces IRR rate.Ocular toxicity (keratopathy, blurred vision) in majority of patients; thrombocytopenia and infusion reactions.
Toxicology
CRS
N/A—
Clinical
Safety signal
Infusion-related reactions (premedication required), cytopenias, and increased infection risk; subcutaneous formulation reduces IRR rate.Ocular toxicity (keratopathy, blurred vision) in majority of patients; thrombocytopenia and infusion reactions.
Clinical
Program phase
APPROVEDAPPROVED
Clinical
Trial activity
No active/completed countsNo active/completed counts