Belantamab Mafodotin

drug
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Also known as Belantamab mafodotin blmfBelantamab mafodotin-blmfBelantamab mafodotinaBelantamab mafodotineBlenrepGSK-2857916GSK2857916

Summary

Belantamab Mafodotin (CHEMBL4298209) is an approved antibody drug conjugate (ATC L01FX15) targeting TNFRSF17; indicated across 5 conditions including plasma cell myeloma and neoplasm.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Antibody drug conjugate
  • ATC class: L01FX15
  • Targets: 1 (TNFRSF17)
  • Indications: 5 conditions
  • Clinical trials: 67

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4298209
NameBelantamab Mafodotin
TypeAntibody drug conjugate
Max phase4
ATCL01FX15

Also known as: Belantamab mafodotin, Belantamab mafodotin blmf, Belantamab mafodotin-blmf, Belantamab mafodotina, Belantamab mafodotine, Blenrep, GSK-2857916, GSK2857916, BELANTAMAB MAFODOTIN

Targets

Targets

Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).

GeneTargetActionpAffinityCancer dependencyUniProt
TNFRSF17B cell maturation antigenBinding9.820.1%Q02223

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

Aggregated over 1 target gene(s): TNFRSF17.

Top Reactome pathways

1 total, by targets touching each:

PathwayTargetsGenes
TNFs bind their physiological receptors1TNFRSF17

Dominant GO biological processes

GO termTargets
adaptive immune response1
lymphocyte homeostasis1
signal transduction1
tumor necrosis factor-mediated signaling pathway1
immune system process1

Indications & clinical

Indications

2 approved indications. FDA phase 4, plus an anticancer drug’s labelled cancer uses (which ChEMBL often logs at phase 3).

IndicationPhaseMONDOEFO
plasma cell myeloma4MONDO:0009693EFO:0001378
neoplasm4MONDO:0005070EFO:0000616

3 diseases in clinical trials (phase 1–3, investigational — not approved indications). Highest ChEMBL trial phase per disease; a non-cancer approved use is occasionally logged at phase 3 here.

Disease (in trials)PhaseMONDOEFO
diffuse large B-cell lymphoma2MONDO:0018905EFO:0000403
hereditary amyloidosis2MONDO:0018634MONDO:0019438
amyloidosis1MONDO:0019065EFO:1001875

Clinical trials

Total trials: 67.

Phase distribution

PhaseTrials
PHASE1/PHASE225
PHASE217
PHASE111
PHASE39
Not specified5

Top trials by phase / activity

NCTPhaseStatusTitle
NCT04162210PHASE3ACTIVE_NOT_RECRUITINGStudy of Single Agent Belantamab Mafodotin Versus Pomalidomide Plus Low-dose Dexamethasone (Pom/Dex) in Participants With Relapsed/Refractory Multiple Myeloma (RRMM)
NCT04246047PHASE3ACTIVE_NOT_RECRUITINGEvaluation of Efficacy and Safety of Belantamab Mafodotin, Bortezomib and Dexamethasone Versus Daratumumab, Bortezomib and Dexamethasone in Participants With Relapsed/Refractory Multiple Myeloma
NCT04484623PHASE3ACTIVE_NOT_RECRUITINGBelantamab Mafodotin Plus Pomalidomide and Dexamethasone (Pd) Versus Bortezomib Plus Pd in Relapsed/Refractory Multiple Myeloma
NCT06679101PHASE3RECRUITINGA Study of Belantamab Mafodotin Administered in Combination With Lenalidomide and Dexamethasone (BRd) Versus Daratumumab, Lenalidomide, and Dexamethasone (DRd) in Participants With Newly Diagnosed Multiple Myeloma (NDMM) Who Are Ineligible for Autologous Stem Cell Transplantation (TI-NDMM)
NCT06868654PHASE3ACTIVE_NOT_RECRUITINGChina Subpopulation: Evaluation of Efficacy and Safety of Belantamab Mafodotin, Bortezomib and Dexamethasone Versus Daratumumab, Bortezomib and Dexamethasone in Participants With Relapsed/Refractory Multiple Myeloma
NCT06868667PHASE3ACTIVE_NOT_RECRUITINGJapan Expansion Cohort: Evaluation of Efficacy and Safety of Belantamab Mafodotin, Bortezomib and Dexamethasone Versus Daratumumab, Bortezomib and Dexamethasone in Participants With Relapsed/Refractory Multiple Myeloma
NCT06956170PHASE3ACTIVE_NOT_RECRUITINGAll Japanese Population: Belantamab Mafodotin Plus Pomalidomide and Dexamethasone (Pd) Versus Bortezomib Plus Pd in Relapsed/Refractory Multiple Myeloma
NCT04549363PHASE3TERMINATEDCharacterization of Corneal Epithelial Changes in Participants Treated With Belantamab Mafodotin
NCT05461209PHASE3WITHDRAWNA Study of Comparing Talquetamab to Belantamab Mafodotin in Participants With Relapsed/Refractory Multiple Myeloma
NCT02343042PHASE1/PHASE2ACTIVE_NOT_RECRUITINGSelinexor and Backbone Treatments of Multiple Myeloma Patients
NCT04126200PHASE1/PHASE2ACTIVE_NOT_RECRUITINGPlatform Study of Belantamab Mafodotin as Monotherapy and in Combination With Anti-cancer Treatments in Participants With Relapsed/Refractory Multiple Myeloma (RRMM)
NCT04643002PHASE1/PHASE2RECRUITINGIsatuximab in Combination With Novel Agents in RRMM - Master Protocol
NCT04680468PHASE2ACTIVE_NOT_RECRUITINGStudy of Belantamab Mafodotin as Pre- and Post-autologous Stem Cell Transplant and Maintenance for Multiple Myeloma
NCT04802356PHASE2ACTIVE_NOT_RECRUITINGBelantamab Mafodotin in Newly Diagnosed Transplant Eligible Multiple Myeloma Patients
NCT04808037PHASE1/PHASE2ACTIVE_NOT_RECRUITINGBlmf, Lenalidomide and Dexamethasone in Transplant-ineligible Patients With Newly Diagnosed Multiple Myeloma
NCT04822337PHASE1/PHASE2ACTIVE_NOT_RECRUITINGStudy of Carfilzomib, Lenalidomide, Dexamethasone and Belantamab Mafodotin in Multiple Myeloma
NCT04876248PHASE2ACTIVE_NOT_RECRUITINGBelantamab Mafodotin and Lenalidomide for the Treatment of Multiple Myeloma in Patients With Minimal Residual Disease Positive After Stem Cell Transplant
NCT05002816PHASE1/PHASE2ACTIVE_NOT_RECRUITINGNovel Combination of Belantamab Mafodotin and Elotuzumab to Enhance Therapeutic Efficacy in Multiple Myeloma
NCT05060627PHASE1/PHASE2ACTIVE_NOT_RECRUITINGStudy of Belantamab Mafodotin in Combination With Kd for the Treatment of Relapsed Myeloma Patients, Refractory to Lenalidomide
NCT05091372PHASE2RECRUITINGMinimal Residual Disease Guided Maintenance Therapy With Belantamab Mafodotin and Lenalidomide After Autologous Hematopoietic Cell Transplantation in Patients With Newly Diagnosed Multiple Myeloma
NCT05145816PHASE1/PHASE2RECRUITINGPhase 1/2a Study of Belantamab Mafodotin in Relapsed or Refractory AL Amyloidosis
NCT05208307PHASE2RECRUITINGBelantamab Mafodotin, Pomalidomide and Dexamethasone for the Treatment of High-Risk Myeloma
NCT05573802PHASE1/PHASE2RECRUITINGA Study to Investigate Safety and Clinical Activity of Belantamab Mafodotin in Combination With Lenalidomide, Dexamethasone and Nirogacestat in Patients With Transplant Ineligible Newly Diagnosed Multiple Myeloma
NCT05581875PHASE1/PHASE2NOT_YET_RECRUITINGA Study to Investigate the Safety and Clinical Activity of Belantamab Mafodotin in Combination With Daratumumab, Pomalidomide and Dexamethasone in Patients With Relapsed/ Refractory Multiple Myeloma Previously Treated With One Line Therapy Who Are Lenalidomide Refractory
NCT05714839PHASE1/PHASE2RECRUITINGA Study to Investigate the Safety and Efficacy of Belantamab for the Treatment of Multiple Myeloma When Used as Monotherapy and in Combination Treatments
NCT05789303PHASE2RECRUITINGStudy of Belantamab Mafodotin With Carfilzomib, Pomalidomide, and Dexamethasone in Relapsed Multiple Myeloma
NCT05847569PHASE2RECRUITINGAlternate Doses and Dosing Schedules of Belantamab Mafodotin for Treatment of Triple-Class Refractory Multiple Myeloma
NCT05853965PHASE1/PHASE2RECRUITINGCombination Treatment of Belantamab Mafodotin and Venetoclax in Treatment of Relapsed and Refractory t(11;14) Multiple Myeloma
NCT05874193PHASE2NOT_YET_RECRUITINGA Collaborative Community Effort Using Belantamab Mafodotin in Relapsed/Refractory Myeloma
NCT05922501PHASE2RECRUITINGIsatuximab, Bela Maf, Pom, and Dex in Relapsed/Refractory Multiple Myeloma
NCT06232044PHASE1/PHASE2RECRUITINGTesting the Combination of Two Approved Drugs and One Experimental Drug in Patients With Relapsed or Refractory Multiple Myeloma
NCT07019545PHASE2NOT_YET_RECRUITINGA PHASE II TRIAL AIMING TO INVESTIGATE THE SAFETY AND CLINICAL ACTIVITY OF BELANTAMAB MAFODOTIN IN ADULT PATIENTS WITH PRIMARY IMMUNE THROMBOCYTOPENIA PREVIOUSLY TREATED WITH A THROMBOPOIETIN RECEPTOR AGONIST AND/OR RITUXIMAB AFTER CORTICOSTEROID FIRST-LINE THERAPY
NCT07084896PHASE1/PHASE2ACTIVE_NOT_RECRUITINGSub-study of Belantamab Mafodotin (GSK2857916) in Combination With Nirogacestat in Participants With RRMM
NCT07150091PHASE1/PHASE2ACTIVE_NOT_RECRUITINGSub-study of Belantamab Mafodotin (GSK2857916) in Combination With Nirogacestat, Lenalidomide, and Dexamethasone in Participants With RRMM
NCT07150104PHASE1/PHASE2ACTIVE_NOT_RECRUITINGSub-study of Belantamab Mafodotin (GSK2857916) as Monotherapy and in Combination With Nirogacestat, Pomalidomide, and Dexamethasone in Participants With RRMM
NCT07217119PHASE1/PHASE2ACTIVE_NOT_RECRUITINGSub-study of Belantamab Mafodotin (GSK2857916) in Combination With Feladilimab (GSK3359609) in Participants With RRMM
NCT07217184PHASE1/PHASE2ACTIVE_NOT_RECRUITINGSub-study of Belantamab Mafodotin (GSK2857916) in Combination With Isatuximab in Participants With RRMM
NCT07224672PHASE2NOT_YET_RECRUITINGA Study to Evaluate the Efficacy and Safety of Belantamab Mafodotin in Combination With Cyclophosphamide, Bortezomib, and Dexamethasone in Adult Participants With Newly Diagnosed Amyloid Light Chain (AL) Amyloidosis
NCT07227311PHASE2RECRUITINGA Study to Evaluate the Efficacy and Safety of Belantamab Mafodotin in Combination With Standard of Care in Participants With Relapsed-Refractory Multiple Myeloma (RRMM)
NCT07614360PHASE2NOT_YET_RECRUITINGStudy of Alternative and Approved Dosing Regimens of Belantamab Mafodotin, Bortezomib, and Dexamethasone (BVd) in Participants With Relapsed/Refractory Multiple Myeloma
NCT03544281PHASE1/PHASE2COMPLETEDTo Evaluate Safety, Tolerability, and Clinical Activity of the Antibody-drug Conjugate, GSK2857916 Administered in Combination With Lenalidomide Plus Dexamethasone (Arm A), or in Combination With Bortezomib Plus Dexamethasone (Arm B) in Participants With Relapsed/Refractory Multiple Myeloma (RRMM)
NCT03732703PHASE1/PHASE2COMPLETEDMyeloma-Developing Regimens Using Genomics (MyDRUG)
NCT03848845PHASE1/PHASE2COMPLETEDStudy Evaluating Safety, Tolerability and Clinical Activity of GSK2857916 in Combination With Pembrolizumab in Subjects With Relapsed/Refractory Multiple Myeloma (RRMM)
NCT04617925PHASE2COMPLETEDA Study of Belantamab Mafodotin in Patients With Relapsed or Refractory AL Amyloidosis
NCT04676360PHASE2TERMINATEDBelantamab Mafodotin In Plasmablastic Lymphoma & ALK+ Large B-Cell Lymphoma
NCT05064358PHASE2COMPLETEDStudy to Investigate Alternative Dosing Regimens of Belantamab Mafodotin in Participants With Relapsed or Refractory Multiple Myeloma
NCT05117008PHASE2TERMINATEDMaintenance Belantamab Mafodotin (Blenrep®) After B-cell Maturation Antigen-Directed Chimeric Antigen Receptor T-cell Therapy in Patients With Relapsed and/or Refractory Multiple Myeloma
NCT05280275PHASE1/PHASE2UNKNOWNA Study to Investigate the Safety and Clinical Activity of Belantamab Mafodotin in Combination With Daratumumab, Lenalidomide and Dexamethasone in Patients With Newly Diagnosed Multiple Myeloma Transplant Ineligible
NCT05493618PHASE1/PHASE2WITHDRAWNPembrolizumab, Belantamab and Dexamethasone in Refractory Multiple Myeloma.
NCT06160609PHASE1/PHASE2TERMINATEDPlatform Sub-study of Belantamab Mafodotin (GSK2857916) in Combination With aOX40 (GSK3174998) in Participants With RRMM
NCT06655818PHASE1/PHASE2TERMINATEDSub-study of Belantamab Mafodotin (GSK2857916) as Monotherapy and in Combination With Dostarlimab (GSK4057190) in Participants With RRMM
NCT04091126PHASE1ACTIVE_NOT_RECRUITINGStudy of Belantamab Mafodotin Plus Standard of Care (SoC) in Newly Diagnosed Multiple Myeloma
NCT04398745PHASE1ACTIVE_NOT_RECRUITINGA Study of Belantamab Mafodotin Monotherapy in Multiple Myeloma Participants With Normal and Varying Degree of Impaired Renal Function
NCT05055063PHASE1RECRUITINGA Phase 1 With Extension Cohort, Single Arm, Single Center, Open Label Trial of Belantamab Mafodotin for the Treatment of High-Risk Smoldering Multiple Myeloma
NCT05556798PHASE1ACTIVE_NOT_RECRUITINGA Study of Belantamab Mafodotin in Combination With Nirogacestat and Pomalidomide in People With Multiple Myeloma That Has Not Responded to Treatment or Has Come Back After Treatment
NCT07609706PHASE1NOT_YET_RECRUITINGA Study of the Combination of Belantamab Mafodotin, Bortezomib, and Dexamethasone (BVd) in Participants With Multiple Myeloma and Moderate Hepatic Impairment
NCT02064387PHASE1COMPLETEDDose Escalation Study to Investigate the Safety, Pharmacokinetics, Pharmacodynamics, Immunogenicity and Clinical Activity of GSK2857916
NCT03828292PHASE1COMPLETEDAn Open-label, Dose Escalation Study in Japanese Participants With Relapsed/Refractory Multiple Myeloma Who Have Failed Prior Anti Myeloma Treatments
NCT04177823PHASE1COMPLETEDA Study of Belantamab Mafodotin to Investigate Safety, Tolerability, Pharmacokinetics, Immunogenicity and Clinical Activity in Participants With Relapsed/Refractory Multiple Myeloma (RRMM)
NCT04398680PHASE1WITHDRAWNA Study of Belantamab Mafodotin in Multiple Myeloma Participants With Normal and Impaired Hepatic Function
NCT04892264PHASE1TERMINATEDBelantamab Mafodotin, Lenalidomide, and Daratumumab for the Treatment of Relapsed, Refractory, or Previously Untreated Multiple Myeloma
NCT05065047PHASE1TERMINATEDBelantamab Mafadotin Maintenance Therapy After Salvage Autologous Hematopoietic Cell Transplantation in Patients With Relapse Refractory Multiple Myeloma
NCT03763370Not specifiedAVAILABLEManaged Access Program for Combination Treatment With Belantamab Mafodotin in Multiple Myeloma
NCT05297240Not specifiedUNKNOWNRetrospective Study of the Use of Belantamab Mafodotin (Blenrep®) in Patients With Relapsed and/or Refractory Multiple Myeloma (RRMM) in Spain.
NCT05393024Not specifiedCOMPLETEDPatient With MMRR Treated With Belantamab Mafotidine on Monotherapy
NCT05833737Not specifiedTERMINATEDCorneal Findings in Patients Treated With Belantamab Mafodotin
NCT05986682Not specifiedCOMPLETEDReal-World Analysis of Belantamab Mafodotin Care Patterns in Patients With Relapsed and/or Refractory Multiple Myeloma

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).