NDAINTRAVENOUSSOLUTIONPriority Review
Approved
May 1998
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Clinical Trials
10
Data completeness
3/8 — Basic
Priority Review
Drug data last refreshed 23h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
AGGRASTAT (tirofiban) is an intravenous glycoprotein IIb/IIIa inhibitor platelet aggregation inhibitor used in acute coronary syndromes and percutaneous coronary intervention. It works by blocking platelet aggregation to prevent thrombotic events in patients at high risk for ischemic complications.
LOE Approaching
Product is approaching loss of exclusivity with limited remaining commercial runway; expect smaller team size and cost-containment focus.
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 (10)
Tirofiban After Successful MT Recanalization in AIS
Started Apr 2024
1,380 enrolled
Acute Ischemic StrokeVessel Occlusion
Efficacy and Safety of Tirofiban for Patients With BAD (BRANT)
Started Nov 2023
516 enrolled
Branch Atheromatous Disease
Antiplatelet Effects of Tirofiban vs. Cangrelor N-STEMI Patients Undergoing Percutaneous Coronary Intervention
Started Aug 2017
10 enrolled
Non-ST Elevation Myocardial Infarction (NSTEMI)
Pharmacokinetic Evaluation of Tirofiban Using a Single High-Dose Bolus In Subjects With Varying Degrees of Renal Function
Started Jan 2013
25 enrolled
Renal Insufficiency
Comparison of Antiplatelet Effect of Ticagrelor vs Tirofiban in Patients With Non-ST Elevation Acute Coronary Syndrome
Started Aug 2012
100 enrolled
Non-ST Segment Elevation Acute Coronary Syndrome
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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.