NDAINJECTIONINJECTABLE
Approved
Jan 2012
Lifecycle
Peak
Competitive Pressure
30/100
Clinical Trials
2
Data completeness
4/8 — Partial
ARGATROBAN (argatroban) by Hikma is thrombin inhibitors [moa]. First approved in 2012.
Drug data last refreshed 8h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
Argatroban is a direct thrombin inhibitor administered via injection for anticoagulation therapy. It is indicated for patients with heparin-induced thrombocytopenia (HIT) who require continued anticoagulation. The drug works by reversibly binding to the active site of thrombin, preventing thrombin-catalyzed reactions.
Peak
Argatroban is at peak commercial maturity with moderate competitive pressure (30), suggesting stable but competitive team engagement and sales infrastructure.
Mechanism of Action
Thrombin Inhibitors
Pharmacologic Class:
Anti-coagulant
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (2)
Significance of Antibodies to Heparin/Platelet Factor 4 Complex in Vein Graft Patency and Potential Role of Argatroban for Prevention of Vein Graft Occlusion
Started Nov 2010
9 enrolled
Coronary Artery Bypass Graft SurgeryPresence of Heparin/Platelet Factor 4 Antibody
Evaluation of Argatroban Injection in Pediatric Patients Requiring Anticoagulant Alternatives to Heparin
Started Sep 2003
24 enrolled
ThrombocytopeniaThrombosis
Career Relevance
Working on Argatroban positions professionals in a niche, mature anticoagulation franchise within a specialized hospital setting, offering stability but limited growth trajectory. Career progression will depend on competitive retention of HIT market share and potential label expansions rather than blockbuster growth opportunities.
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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.