NDAINTRAVENOUSINJECTABLE
Approved
Oct 2013
Lifecycle
LOE Approaching
Competitive Pressure
15/100
Clinical Trials
1
Data completeness
6/8 — Strong
VIZAMYL (flutemetamol f-18) by GE HealthCare is radiopharmaceutical activity [moa]. Approved for radioactive diagnostic agent [epc]. First approved in 2013.
Drug data last refreshed 19h ago · AI intelligence enriched 2w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
VIZAMYL (flutemetamol F-18) is a radioactive diagnostic agent administered intravenously for positron emission tomography (PET) imaging. It is used to visualize amyloid pathology in the brain, aiding in the diagnosis and assessment of neurodegenerative diseases such as Alzheimer's disease. The drug works by binding to amyloid-beta deposits, enabling clinicians to detect and monitor cerebral amyloid burden.
LOE Approaching2.4 years to LOE
Product is approaching loss of exclusivity with 2.4 years remaining on formulation patents; expect team consolidation and transition focus toward managed decline and lifecycle extension strategies.
Mechanism of Action
Radiopharmaceutical Activity
Pharmacologic Class:
Radioactive Diagnostic Agent
Indications (1)
Clinical Trials (1)
A Study to Evaluate the Effectiveness of VIZAMYL™ Reader Training Programme in Europe
Started Dec 2018
227 enrolled
Cognitive Impairment
Why This Matters for Your Career
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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.