Last reviewed · How we verify

integrilin

University of Cincinnati · Phase 1 active Small molecule ✓ Verified Jun 2026

integrilin is a Small molecule drug developed by University of Cincinnati. It is currently in Phase 1 development for Acute coronary syndrome, NonQ wave myocardial infarction, Percutaneous coronary intervention.

Eptifibatide is an antiplatelet drug that belongs to the class of integrin alpha-IIb/beta-3 inhibitors, which reversibly binds to platelets. It is used to treat conditions such as stroke, acute coronary syndrome, and coronary artery disease, often in combination with other medications like aspirin.

Likelihood of approval
7.6% vs 9.6% industry baseline
If approved by FDA: likely 2033–2036
Steps remaining: Phase 2 → Phase 3 → NDA/BLA submission
Confidence: Medium
Why this estimate
  • Baseline phase 1 → approval rate +9.6pp
    Industry-wide phase 1 drugs reach approval ~9.6% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas).
  • Cardiovascular Phase 3 risk -2.0pp
    Modern cardiovascular outcome trials are large + long; many fail to beat aggressive standard-of-care.
Predicted approval windows by jurisdiction (conditional on FDA approval)
Regulator Country Likely year Lag vs FDA
FDA US 2033–2036
EMA EU 2034–2037 +0.7 yr
MHRA GB 2034–2037 +0.7 yr
Health Canada CA 2034–2038 +0.9 yr
TGA AU 2034–2038 +1.2 yr
PMDA JP 2034–2038 +1.5 yr
NMPA CN 2035–2039 +2.3 yr
MFDS KR 2034–2038 +1.4 yr
CDSCO IN 2034–2039 +1.8 yr
ANVISA BR 2035–2039 +2.3 yr

Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).

Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.

At a glance

Generic nameintegrilin
SponsorUniversity of Cincinnati
TargetIntegrin alpha-IIb/beta-3
ModalitySmall molecule
Therapeutic areaCardiovascular
PhasePhase 1

Approved indications

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:

Frequently asked questions about integrilin

What is integrilin?

integrilin is a Small molecule drug developed by University of Cincinnati, indicated for Acute coronary syndrome, NonQ wave myocardial infarction, Percutaneous coronary intervention.

What is integrilin used for?

integrilin is indicated for Acute coronary syndrome, NonQ wave myocardial infarction, Percutaneous coronary intervention, Unstable angina.

Who makes integrilin?

integrilin is developed by University of Cincinnati (see full University of Cincinnati pipeline at /company/university-of-cincinnati).

What development phase is integrilin in?

integrilin is in Phase 1.

What does integrilin target?

integrilin targets Integrin alpha-IIb/beta-3.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing