Ociperlimab

drug
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Also known as Bgb-a1217BGBA-1217BGBA1217

Summary

Ociperlimab (CHEMBL4650411) is a phase-3 clinical-stage antibody; indicated across 9 conditions including neoplasm and non-small cell lung carcinoma.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Antibody
  • Indications: 9 conditions
  • Clinical trials: 13

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4650411
NameOciperlimab
TypeAntibody
Max phase3

Also known as: Bgb-a1217, BGB-A1217, BGBA-1217, BGBA1217, Ociperlimab, OCIPERLIMAB

Targets

Targets

No target linkage available.

Bioactivity

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

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

9 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
neoplasm3MONDO:0005070EFO:0000616
non-small cell lung carcinoma3MONDO:0005233EFO:0003060
esophageal squamous cell carcinoma2MONDO:0005580EFO:0005922
hepatocellular carcinoma2MONDO:0007256EFO:0000182
small cell lung carcinoma2MONDO:0008433EFO:0000702
breast neoplasm2MONDO:0021100MONDO:0007254
diffuse large B-cell lymphoma1MONDO:0018905EFO:0000403

2 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 13.

Phase distribution

PhaseTrials
PHASE27
PHASE34
PHASE1/PHASE21
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT04164199PHASE3ACTIVE_NOT_RECRUITINGStudy of Tislelizumab, Pamiparib, and Other Investigational Agents in Participants With Advanced Malignancies
NCT04746924PHASE3TERMINATEDA Study of Ociperlimab With Tislelizumab Compared to Pembrolizumab in Participants With Untreated Lung Cancer
NCT04866017PHASE3TERMINATEDA Study to Compare Ociperlimab Plus Tislelizumab Versus Durvalumab Following Concurrent Chemoradiotherapy (cCRT) in Participants With Stage III Unresectable Non-Small Cell Lung Cancer
NCT05791097PHASE3WITHDRAWNStudy of Efficacy and Safety of Ociperlimab in Combination With Tislelizumab and Platinum-based Doublet Chemotherapy as First-line Treatment for Participants With Locally Advanced or Metastatic NSCLC.
NCT04693234PHASE2COMPLETEDAdvanTIG-202: Anti-PD-1 Monoclonal Antibody Tislelizumab (BGB-A317) Combined With or Without Anti-TIGIT Monoclonal Antibody Ociperlimab (BGB-A1217) in Participants With Previously Treated Recurrent or Metastatic Cervical Cancer
NCT04732494PHASE2COMPLETEDAnti-PD-1 Monoclonal Antibody Tislelizumab (BGB-A317) Combined With or Without Anti-TIGIT Monoclonal Antibody Ociperlimab (BGB-A1217) in Participants With Recurrent or Metastatic Esophageal Squamous Cell Carcinoma
NCT04948697PHASE2COMPLETEDA Study Investigating the Efficacy and Safety of Ociperlimab and Tislelizumab and BAT1706 Combinations in Patients With Advanced HCC
NCT04952597PHASE2COMPLETEDStudy of Ociperlimab Plus Tislelizumab Plus Chemoradiotherapy in Participants With Untreated Limited-Stage Small Cell Lung Cancer
NCT05014815PHASE2COMPLETEDOciperlimab With Tislelizumab and Chemotherapy in Participants With Untreated Metastatic Non-Small Cell Lung Cancer
NCT05267054PHASE1/PHASE2COMPLETEDTreatment of Relapsed or Refractory Diffuse Large B Cell Lymphoma With Ociperlimab (BGB-A1217) in Combination With Tislelizumab (BGB-A317) or Rituximab
NCT05577702PHASE2COMPLETEDEfficacy, Safety, and Pharmacodynamics of Tislelizumab Monotherapy and Multiple Tislelizumab-based Immunotherapy Combinations in Participants With Resectable Non-Small Cell Lung Cancer
NCT05809895PHASE2WITHDRAWNPhase II Study Evaluating the Efficacy and Safety of Ociperlimab in Combination With Tislelizumab and Chemotherapy as First-line Treatment for Participants With Advanced Triple Negative Breast Cancer
NCT04047862PHASE1COMPLETEDStudy of Ociperlimab (BGB-A1217) in Combination With Tislelizumab in Advanced Solid Tumors

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).