Wilate - von Willebrand Factor/Coagulation Factor VIII Complex (Human)
LOE Approachingvon willebrand factor/coagulation factor viii complex (human)
BLAINTRAVENOUSPOWDER, FOR SOLUTION
Approved
Dec 2009
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Data completeness
1/8 — Limited
Drug data last refreshed 2h ago · AI intelligence enriched 2w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
Wilate is a plasma-derived von Willebrand Factor/Coagulation Factor VIII complex indicated for treatment and prevention of bleeding in von Willebrand disease and hemophilia A patients. It replaces deficient or dysfunctional clotting factors through intravenous administration, restoring hemostatic function in patients with inherited bleeding disorders.
LOE Approaching
Product approaching loss of exclusivity with moderate competitive pressure (30/100), signaling potential team restructuring and transition planning in coming years.
Mechanism of Action
Pharmacologic Class:
Blood Coagulation Factors
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Career Relevance
Wilate presents a career opportunity in a mature therapeutic area requiring expertise in managed care, payer negotiations, and competitive positioning. Professionals joining this product should expect focus on market defense and lifecycle extension rather than launch or rapid growth initiatives.
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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.