ENTYVIO
GrowthmAbBLAINTRAVENOUSINJECTABLE
Approved
Apr 2024
Lifecycle
Growth
Competitive Pressure
30/100
Clinical Trials
6
Data completeness
3/8 — Basic
Drug data last refreshed 2h ago · AI intelligence enriched 1mo ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
ENTYVIO (vedolizumab) is a monoclonal antibody that selectively blocks α4β7 integrin-mediated T-lymphocyte migration into inflamed gastrointestinal tissue. It is indicated for ulcerative colitis and Crohn's disease by preventing the interaction between α4β7 integrin and MAdCAM-1 on gut endothelium. This gut-selective mechanism avoids systemic immunosuppression while targeting chronic GI inflammation.
$0.1BPart D
GrowthIn growth phase with $100M annual Part D spending and ~12K claims, ENTYVIO supports expanding commercial teams focused on gastroenterology market penetration.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (6)
Study to Investigate Comparative Pharmacokinetics, Safety, Immunogenicity and Tolerability Between AVT80 and Entyvio
Started Feb 2025
385 enrolled
Healthy Male and Female Subjects
Study to Investigate Comparative Efficacy, Safety and Immunogenicity Between AVT16 and Entyvio
Started Sep 2024
301 enrolled
Ulcerative Colitis
Efficacy, Safety and Immunogenicity of the Proposed Biosimilar Vedolizumab PB016 in Comparison With Entyvio®
Started Jul 2023
750 enrolled
Ulcerative Colitis
ENTYVIO in Bio-naive Patients With Moderate/Severe Crohn's Disease (CD) in Daily Practice
Started Sep 2020
0Crohn Disease
Development of a Biomarker of Efficacy of Vedolizumab (EnTyvio®) in Patients With ulcErative ColiTis (DETECT)
Started Jan 2017
19 enrolled
ULCERATIVE COLITIS
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.