Zigakibart

drug
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Also known as Bion 1301BION-1301BION1301C-90401C90401

Summary

Zigakibart (CHEMBL5095316) is a phase-3 clinical-stage antibody; indicated across 2 conditions including iga glomerulonephritis and plasma cell myeloma.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Antibody
  • Indications: 2 conditions
  • Clinical trials: 5

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL5095316
NameZigakibart
TypeAntibody
Max phase3

Also known as: Bion 1301, BION-1301, BION1301, C-90401, C90401, Zigakibart, ZIGAKIBART

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

2 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
IgA glomerulonephritis3MONDO:0005342EFO:0004194
plasma cell myeloma1MONDO:0009693EFO:0001378

Clinical trials

Total trials: 5.

Phase distribution

PhaseTrials
PHASE32
PHASE1/PHASE21
PHASE21
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05852938PHASE3ACTIVE_NOT_RECRUITINGA Study of Zigakibart in Adults With IgA Nephropathy
NCT06858319PHASE3RECRUITINGOpen-label Extension Study of Zigakibart in Adults With IgA Nephropathy.
NCT07146906PHASE2RECRUITINGA Study to Assess the Effects of Zigakibart on IgA Nephropathy.
NCT03340883PHASE1/PHASE2TERMINATEDSafety and Tolerability of BION-1301 in Adults With Relapsed or Refractory Multiple Myeloma (MM)
NCT05508204PHASE1COMPLETEDOpen-label Safety and PK Study of BION-1301 in Japanese Healthy Subjects

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).