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About Integrin alpha4beta7

Integrin alpha4beta7 (α4β7) is a cell surface receptor mediating leukocyte trafficking, especially to the gut, by binding to MAdCAM-1 on endothelial cells. This interaction facilitates immune cell adhesion and infiltration, driving inflammation in target tissues. α4β7 is thus a key player in immune responses.

3
Approved Drugs
3
Companies
5
Indications
2
Therapeutic Areas
Broadest Approval
TYRUKO
Novartis
2
approved indications

Top Integrin alpha4beta7 Drugs

TYRUKO
Novartis
2 indications · 2023
TYSABRI
Biogen
2 indications · 2004
ENTYVIO
Takeda
2 indications · 2014
🏢

The competitive landscape includes Novartis, Takeda, and Biogen, each with an approved drug.

Integrin alpha4beta7 Drug Modality Landscape

Modalities

Antibody
2
67%
Biologic (other)
1
33%

Routes of Administration

💉 Injection
1
33%
💧 Other
1
33%
💉 IV
1
33%
💡

Integrin alpha4beta7 is exclusively targeted by antibodies, suggesting it may be a cell-surface or secreted protein.

Consider novel modalities to differentiate from existing antibody-based therapies and capture market share.

Biologics only

📈 Modality Evolution

2004 — Antibody (TYSABRI)
2023 — Biologic (other) (TYRUKO)

Antibodies pioneered Integrin alpha4beta7 targeting (2004), with other biologics entering more recently (2023).

2 drugs pre-2015 1 drug since 2015

Integrin alpha4beta7 Clinical Trials 129 trials

Phase 1-4 trials started in 2008 or later that test an FDA-approved drug acting on Integrin alpha4beta7. Source: ClinicalTrials.gov. How we count

129
Total Trials
34
Active
66
Completed
69%
Completion Rate

Completion by Phase

Phase Total Completed Stopped Active Completion
Phase 1 20 14 4 2 78%
Phase 2 29 14 6 9 70%
Phase 3 32 15 7 10 68%
Phase 4 48 23 12 13 66%

Top Sponsors

Takeda 41 86%
Biogen 22 55%
Millennium Pharmaceuticals, ... 7 71%
Centre Hospitalier Universit... 2 0%
M.D. Anderson Cancer Center 2
Alvotech Swiss AG 2 50%
Therakos LLC 2 0%
Washington University School... 2 100%

By Modality

Antibody
129 69%
Source: ClinicalTrials.gov · Completion rate = completed ÷ (completed + terminated + withdrawn)

Phase 3 Readout Calendar Pro

3 Phase 3 trials testing approved Integrin alpha4beta7 drugs across all sponsors.

Full calendar →
Q2 2027
Vedolizumab
Takeda · Crohn's Disease
Estimated · stale NCT06227910
Q3 2028
Risankizumab
AbbVie · Ulcerative Colitis
Estimated · aging NCT06880744
Q4 2029
Vedolizumab
Takeda · Pouchitis
Estimated · stale NCT06443502

Coverage: trials whose intervention is an approved drug targeting Integrin alpha4beta7. Pre-approval candidates with development codes (e.g. AZD0901, MK-7240) are not yet linked. Anchored on CT.gov primary completion date.

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Competitive Landscape

  • • 3 companies competing
  • • Market share by company

Full Drug Portfolio

  • • All 3 approved drugs
  • • Approval dates & indications

Genetic Validation

  • • Full genetic evidence table
  • • Effect sizes & directions

Approval Timeline

  • • Full 3-drug timeline
  • • First-of-modality markers

Clinical Trials Analysis

  • • Sponsors: 54 (9 companies)
  • • Completion rates by condition
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Full summary • All drugs • Genetic evidence • Trials • Timeline

How We Count Trials

  • Trials: phase 1-4 interventional trials on ClinicalTrials.gov that started in 2008 or later and test an FDA-approved drug acting on Integrin alpha4beta7. A trial counts if an approved drug acting on Integrin alpha4beta7 is in any arm, including as a comparator, and a trial that tests two such drugs counts once. Trials that test only unapproved drugs are not counted. A trial listed as phase 1/2 counts as phase 1, and phase 2/3 as phase 2.
  • Active: recruiting, not yet recruiting, enrolling by invitation, or active and no longer recruiting.
  • Completion rate: of the trials that have ended, the share marked Completed rather than Terminated or Withdrawn. Completed means the trial ended as planned; it does not mean the drug worked. Suspended trials are not counted as ended.
  • Stopped: terminated or withdrawn. Trials stop for many reasons, including slow enrolment and business decisions, not only safety or efficacy.
  • Sponsors: the lead sponsor of each trial. Companies are the sponsors ClinicalTrials.gov classes as industry; the rest are universities, hospitals, cooperative groups, government bodies and individuals.