Vedolizumab

drug
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Also known as EntyvioLDP-02LDP02MLN-0002MLN-02MLN0002MLN02

Summary

Vedolizumab (CHEMBL1743087) is an approved antibody (ATC L04AG05); indicated across 13 conditions including crohn disease and ulcerative colitis.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Antibody
  • ATC class: L04AG05
  • Indications: 13 conditions
  • Clinical trials: 100

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1743087
NameVedolizumab
TypeAntibody
Max phase4
ATCL04AG05

Also known as: Entyvio, LDP-02, LDP02, MLN-0002, MLN-02, MLN0002, MLN02, Vedolizumab, VEDOLIZUMAB

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
integrin α4β7Antagonist8.27

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

13 indications (2 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
Crohn disease4MONDO:0005011EFO:0000384
ulcerative colitis4MONDO:0005101EFO:0000729
pouchitis3MONDO:0005312EFO:0003921
celiac disease2MONDO:0005130EFO:0001060
HIV infectious disease2MONDO:0005109EFO:0000764
colitis2MONDO:0005292EFO:0003872
salivary gland cancer2MONDO:0004669MONDO:0000521
neoplasm2MONDO:0005070MONDO:0004992
melanoma1MONDO:0005105EFO:0000756
inflammatory bowel disease1MONDO:0005265EFO:0003767
type 1 diabetes mellitus0MONDO:0005147MONDO:0005147

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

Clinical trials

Total trials: 100.

Phase distribution

PhaseTrials
PHASE426
Not specified24
PHASE319
PHASE218
PHASE16
PHASE1/PHASE23
EARLY_PHASE13
PHASE2/PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05481619PHASE4RECRUITINGStudy of the Effect of Vedolizumab on Intestinal Microecological Changes and Its Efficacy in the Treatment of Ulcerative Colitis
NCT06045754PHASE4RECRUITINGA Study of Vedolizumab Intravenous (IV) and Adalimumab or Vedolizumab and Ustekinumab in Adults With Crohn’s Disease
NCT06095128PHASE4RECRUITINGA Study of Vedolizumab With Tofacitinib in Adults With Ulcerative Colitis (UC)
NCT06180382PHASE4RECRUITINGComparison of Vedolizumab Treatment to Adalimumab Dose Intensification in Crohn’s Disease Patients With Loss of Response or Biomarker Activity to Adalimumab on First Line With Therapeutic Drug Concentration.
NCT06257706PHASE4RECRUITINGVECTORS - A Study to Evaluate Transmural Healing as a Treatment Target in Crohn’s Disease
NCT06584162PHASE4RECRUITINGSubcutaneous Interval Lengthening of Vedolizumab for Economic Research
NCT06609447PHASE4RECRUITINGThe Efficacy and Safety of Combining Probiotic VSL#3 With Vedolizumab for the Treatment of Moderate Ulcerative Colitis
NCT02324699PHASE4TERMINATEDCorticosteroids With Vedolizumab in Crohn’s Disease
NCT02559713PHASE4COMPLETEDPostmarketing Vedolizumab Milk-Only Lactation Study in Lactating Women With Active Ulcerative Colitis or Crohn’s Disease
NCT02630966PHASE4COMPLETEDVedolizumab IV 300 mg in the Treatment of Fistulizing Crohn’s Disease
NCT02646657PHASE4COMPLETEDAn Open Label Phase 4 Study to Evaluate Efficacy of Early Versus Late Use of Vedolizumab in Ulcerative Colitis
NCT02646683PHASE4COMPLETEDA Study to Evaluate Efficacy, of Early Versus Late Use of Vedolizumab in Crohn’s Disease: the LOVE-CD Study
NCT02743806PHASE4TERMINATEDExtended Access Program of Vedolizumab IV in Ulcerative Colitis and Crohn’s Disease
NCT02760615PHASE4WITHDRAWNPhase 4, Vedolizumab-4002 Post-marketing, Disease-Drug-Drug Interaction Study
NCT02764762PHASE4COMPLETEDTriple Combination Therapy in High Risk Crohn’s Disease (CD)
NCT02768532PHASE4TERMINATEDValue of Pharmacokinetic Assays in the Prediction of Induction and Maintenance Therapeutic Response in Crohn’s Disease
NCT02790138PHASE4COMPLETEDA Study to Evaluate the Efficacy and Safety of Vedolizumab in the Treatment of Chronic Pouchitis
NCT02820493PHASE4WITHDRAWNEffectiveness of Vedolizumab in CD Patients Naïve to Anti-TNF
NCT03237260PHASE4WITHDRAWNAn Open Label Single-arm Phase 4 Study of Vedolizumab in Subjects With Newly Diagnosed Active Ulcerative Colitis
NCT03629379PHASE4COMPLETEDResponse to Ustekinumab for Anti-tnf Induced Psoriasiform Skin Lesions
NCT03679546PHASE4COMPLETEDEFFICACI : EFFicacy of Intravenous Infliximab Versus Vedolizumab After Failure of subCutaneous Anti-TNF in Patients With UlCerative Colitis
NCT04006080PHASE4UNKNOWNInvestigation of the Faecal Loss of Vedolizumab and Its Role in Influencing Serum Drug Levels, Outcomes and Response in Ulcerative Colitis
NCT05205603PHASE4COMPLETEDEfficacy of Mesalazine Combined With Biologics in the Treatment of Moderate to Severe Ulcerative Colitis
NCT06066840PHASE4UNKNOWNVedolizumab, Anti-CD25 Antibody, Rapid Reduction of Glucocorticoids for SR-aGVHD With Gastrointestinal Involvement
NCT06626165PHASE4COMPLETEDAssociation Between Effectiveness of Mirikizumab and UC Patients With High Neutrophilic Infiltration in Epithelium of the Colonic Mucosa
NCT07398586PHASE4COMPLETEDThe Association Between Interleukin-7 Receptor Gene Polymorphism and the Risk of Ulcerative Colitis
NCT04738942PHASE3ACTIVE_NOT_RECRUITINGA Study of Intravenous Vedolizumab Administered Every 4 Weeks in Japanese Participants With Moderate to Severe Ulcerative Colitis or Crohn’s Disease
NCT05515029PHASE3ACTIVE_NOT_RECRUITINGPreventing of GVHD With Post-transplantation Cyclophosphamide, Abatacept, Vedolizumab and Calcineurin Inhibitor at Patients With Hemoblastosis
NCT06227910PHASE3RECRUITINGA Study of Vedolizumab With and Without Upadacitinib in Adults With Crohn’s Disease
NCT06337695PHASE2/PHASE3NOT_YET_RECRUITINGVERIFY: Vedolizumab for the Prevention of Immune Checkpoint Inhibitor Related Diarrhea or Colitis in Patients With Cancer
NCT06443502PHASE3RECRUITINGA Study to Learn About the Safety of Vedolizumab and How Well it Works in Children and Teenagers With Active Chronic Pouchitis
NCT06880744PHASE3ACTIVE_NOT_RECRUITINGA Study to Assess the Change in Disease Activity in Adult Participants With Moderate to Severe Ulcerative Colitis Treated With Risankizumab Compared to Vedolizumab
NCT00783692PHASE3COMPLETEDStudy of Vedolizumab (MLN0002) in Patients With Moderate to Severe Crohn’s Disease
NCT00783718PHASE3COMPLETEDStudy of Vedolizumab (MLN0002) in Patients With Moderate to Severe Ulcerative Colitis
NCT00790933PHASE3COMPLETEDAn Open-label Study of Vedolizumab (MLN0002) in Participants With Ulcerative Colitis and Crohn’s Disease
NCT01224171PHASE3COMPLETEDStudy of Vedolizumab in Patients With Moderate to Severe Crohn’s Disease
NCT02038920PHASE3COMPLETEDPhase III Study of MLN0002 (300 mg) in Treatment of Crohn’s Disease
NCT02039505PHASE3COMPLETEDPhase III Study of MLN0002 (300 mg) in the Treatment of Ulcerative Colitis
NCT02425111PHASE3COMPLETEDEffect of Intravenous (IV) Vedolizumab on Mucosal Healing in Crohn’s Disease
NCT02497469PHASE3COMPLETEDAn Efficacy and Safety Study of Vedolizumab Intravenous (IV) Compared to Adalimumab Subcutaneous (SC) in Participants With Ulcerative Colitis

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).