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항목
ADCCurated CoreFDAstaleApproved
belantamab mafodotin (Blenrep, GSK2857916)
GSK·BCMA
78 trials
ADCLimited DatastalePhase 2
Endoxan (Endoxan)
Celyad Oncology SA·Lymphoma, T-Cell, Peripheral
92 trials
Overview
Program
Blenrep (belantamab mafodotin)Endoxan
Overview
Company
GSKCelyad Oncology SA
Overview
Modality
ADCADC
Overview
Target
BCMALymphoma, T-Cell, Peripheral
Overview
Indication
Multiple myelomaRelapse/Refractory Multiple Myeloma
Overview
Phase
APPROVEDPHASE_2
Overview
Status
DISCONTINUEDACTIVE
Overview
Content status
Curated CoreLimited Data
Overview
Data Confidence
Editorial scope · Curated CoreEditorial scope · limited data
Overview
Development Signal
Development Signal · EstablishedDevelopment Signal · Emerging
Overview
Approval status
FDA approvedInvestigational
Positioning
Key differentiator
BCMA-targeted ADC with ocular AEs—
Positioning
Known limitation
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
Belantamab mafodotin binds BCMA on plasma cells; afucosylated Fc enhances immune engagement while MMAF (microtubule inhibitor) payload is internalized and causes cell death.Targeting Apoptosis Signaling Pathway
MoA
Biomarker
BCMA expression on myeloma cells.biomarker for cancer metastasis
Toxicology
Species
Mouse, Rat—
Toxicology
Animal (cat.)
Human—
Toxicology
Major finding
Ocular toxicity (keratopathy, blurred vision) in majority of patients; thrombocytopenia and infusion reactions.—
Clinical
Safety signal
Ocular toxicity (keratopathy, blurred vision) in majority of patients; thrombocytopenia and infusion reactions.—
Clinical
Program phase
APPROVEDPHASE_2
Clinical
Trial activity
No active/completed countsNo active/completed counts