Visilizumab

drug
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Also known as HUM-291NuvionhuM291

Summary

Visilizumab (CHEMBL2108811) is a phase-3 clinical-stage antibody; indicated across 5 conditions including acute myeloid leukemia and ulcerative colitis.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Antibody
  • Indications: 5 conditions
  • Clinical trials: 13

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL2108811
NameVisilizumab
TypeAntibody
Max phase3

Also known as: HUM-291, Nuvion, Visilizumab, huM291, VISILIZUMAB

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
acute myeloid leukemia3MONDO:0018874EFO:0000222
ulcerative colitis2MONDO:0005101EFO:0000729
Crohn disease2MONDO:0005011EFO:0000384
graft versus host disease2MONDO:0013730MONDO:0013730
lymphoma1MONDO:0005062EFO:0000574

Clinical trials

Total trials: 13.

Phase distribution

PhaseTrials
PHASE25
PHASE2/PHASE33
PHASE32
PHASE1/PHASE22
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00032305PHASE2/PHASE3COMPLETEDResearch Study in Patients With Severe Ulcerative Colitis
NCT00279422PHASE2/PHASE3TERMINATEDA Study of Visilizumab in Subjects With Intravenous Steroid-Refractory Ulcerative Colitis
NCT00279435PHASE2/PHASE3TERMINATEDStudy of Visilizumab Versus Placebo in Subjects With Intravenous Steroid-refractory Ulcerative Colitis Previously Responsive in a Visilizumab Study
NCT00502294PHASE3WITHDRAWNA Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of Visilizumab in Subjects With Intravenous Steroid-Refractory Ulcerative Colitis
NCT04722952PHASE3UNKNOWNPD-1 Inhibitor Combined With Azacytidine and Homoharringtonine,Cytarabine, G-CSF for Refractory or Relapsed AML
NCT00032279PHASE2UNKNOWNResearch Study of Visilizumab for Treatment of Glucocorticoid- Refractory Graft Versus Host Disease
NCT00032292PHASE1/PHASE2COMPLETEDResearch Study of Visilizumab for Treatment of Acute Graft Versus Host Disease
NCT00267306PHASE1/PHASE2COMPLETEDUlcerative Colitis Study: Study of Visilizumab in Patients With Severe Ulcerative Colitis
NCT00267709PHASE2COMPLETEDVisilizumab for Treatment of Perianal Fistulas in Crohn’s Disease
NCT00267722PHASE2COMPLETEDVisilizumab for Moderate to Severe Inflammatory, Nonstricturing, Nonpenetrating Crohn’s Disease
NCT00307827PHASE2TERMINATEDStudy of Visilizumab in Subjects With Intravenous Steroid-Refractory Ulcerative Colitis (IVSR-UC)
NCT00720629PHASE2TERMINATEDVisilizumab for the Prevention of Graft-versus-Host Disease After Allogeneic Hematopoietic Cell Transplantation
NCT00006009PHASE1COMPLETEDMonoclonal Antibody Therapy in Treating Patients With Advanced or Recurrent Lymphoma

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).