Vunakizumab

drug
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Also known as Shr-1314

Summary

Vunakizumab (CHEMBL4298102) is a phase-3 clinical-stage antibody; indicated across 5 conditions including psoriasis and ankylosing spondylitis.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Antibody
  • Indications: 5 conditions
  • Clinical trials: 19

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4298102
NameVunakizumab
TypeAntibody
Max phase3

Also known as: Shr-1314, SHR-1314, Vunakizumab, VUNAKIZUMAB

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

5 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
psoriasis3MONDO:0005083EFO:0000676
ankylosing spondylitis2MONDO:0005306EFO:0003898
lupus nephritis2MONDO:0005556EFO:0005761
psoriatic arthritis2MONDO:0011849EFO:0003778

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

Clinical trials

Total trials: 19.

Phase distribution

PhaseTrials
PHASE17
PHASE34
PHASE24
PHASE42
PHASE2/PHASE31
PHASE1/PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06779097PHASE4NOT_YET_RECRUITINGPhase IV Study: Vunakizumab Efficacy and Safety in Moderate-to-severe Plaque Psoriasis
NCT07373847PHASE4NOT_YET_RECRUITINGVunakizumab Combined With Recaticimab in Subjects With Moderate to Severe Plaque Psoriasis and Dyslipidemia
NCT06640257PHASE3RECRUITINGA Study of the Efficacy and Safety of SHR-1314 for Adult Active Psoriatic Arthritis
NCT06833307PHASE3NOT_YET_RECRUITINGThe Efficacy and Safety of SHR-1314 in the Treatment of Pediatric Patients of Age 6 to <18 Years With Moderate to Severe Plaque Psoriasis
NCT06860750PHASE3RECRUITINGA Trial of SHR-1314 Injection in Adult Patients With Active Non-radiographic Axial Spondyloarthritis
NCT04839016PHASE3UNKNOWNEfficacy 、Safety and PK of SHR-1314 in Patients With Moderate-to-Severe Plaque Psoriasis
NCT04840485PHASE2/PHASE3COMPLETEDEfficacy and Safety of SHR-1314 in Patients With Active Ankylosing Spondylitis
NCT07069270PHASE2NOT_YET_RECRUITINGA Study on the First-line Treatment of Small Cell Lung Cancer With Adebrelimab and Vunakizumab and Chemotherapy
NCT03463187PHASE1/PHASE2COMPLETEDMulti-Dose Study of SHR-1314 in Subjects With Moderate-to-severe Plaque Psoriasis
NCT04924296PHASE2UNKNOWNA Phase II Study to Evaluate the Efficacy and Safety of SHR-1314 in Lupus Nephritis
NCT05055934PHASE2COMPLETEDStudy of the Effectiveness and Safety of SHR-1314 for Psoriatic Arthritis
NCT05394857PHASE2TERMINATEDEfficacy and Safety of SHR-1314 by Subcutaneous Injection in Active Moderate to Severe Graves’ Orbitopathy Patients
NCT06881290PHASE1RECRUITINGVunakizumab for the Treatment of Mild to Moderate Systemic Lupus Erythematosus
NCT02934412PHASE1COMPLETEDA Study of SHR-1314 in Healthy Subjects
NCT03704428PHASE1COMPLETEDSafety, Tolerability and PK of SHR1314 in axSpA
NCT03710681PHASE1UNKNOWNA Safety Study of Multiple Subcutaneous (s.c.) Injections of SHR-1314 in Adults With Moderate-to-severe Plaque Psoriasis
NCT04326881PHASE1UNKNOWNA Study to Compare Pharmacokinetic and Safety Profiles of Different Formulations of SHR-1314 After Subcutaneous Injection in Healthy Subjects
NCT04527484PHASE1UNKNOWNA Bioequivalence Study to Compare Two Formulations of SHR-1314 After Subcutaneous Injection in Healthy Subjects
NCT06182384PHASE1COMPLETEDA Clinical Study to Compare the Safety and Pharmacokinetics of SHR-1314 Injection in Healthy Subjects at Different Specifications Devices

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).