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ST-segment Elevation Myocardial Infarction (STEMI)

1
Pipeline Programs
4
Companies
3
Clinical Trials
2 recruiting
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
0
0
0
0
0
1
Early DiscoveryClinical DevelopmentMarket

Competitive Landscape

4 companies ranked by most advanced pipeline stage

Boston Scientific
Boston ScientificCA - Valencia
1 program
1
No aspirinPhase 41 trial
Active Trials
NCT05709626Recruiting2,258Est. Jan 2028
Medtronic
MedtronicNJ - Phillipsburg
1 program
Export CatheterN/A1 trial
Active Trials
NCT05510661Active Not Recruiting300Est. May 2026
Integrated Biosciences
Integrated BiosciencesCA - San Carlos
1 program
Thrombus aspirationN/A
Autonomous Therapeutics
1 program
Thrombus aspirationN/A1 trial
Active Trials
NCT04212494Recruiting3,838Est. Feb 2026

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
Boston ScientificNo aspirin
MedtronicExport Catheter
Autonomous TherapeuticsThrombus aspiration

Clinical Trials (3)

Total enrollment: 6,396 patients across 3 trials

PRasugrEl Monotherapy Following prImary percUtaneous Coronary Intervention for ST-elevation Myocardial Infarction

Start: Feb 2023Est. completion: Jan 20282,258 patients
Phase 4Recruiting
NCT05510661MedtronicExport Catheter

Use of Export in Primary Percutaneous Coronary Intervention

Start: Jan 2024Est. completion: May 2026300 patients
N/AActive Not Recruiting

Thrombus Aspiration in STEMI Patients With High Thrombus Burden

Start: Aug 2020Est. completion: Feb 20263,838 patients
N/ARecruiting

Phase Legend

PreclinicalLab & animal studies
Phase 1Safety & dosing
Phase 2Efficacy testing
Phase 3Large-scale trials
On MarketApproved & available

Key Insights

2 actively recruiting trials targeting 6,396 patients
4 companies competing in this space

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.