NDAINTRAVENOUSSOLUTION
Approved
May 2020
Lifecycle
Peak
Competitive Pressure
30/100
Data completeness
4/8 — Partial
CERIANNA (fluoroestradiol f 18) by GE HealthCare is positron emitting activity [moa]. Approved for radioactive diagnostic agent [epc]. First approved in 2020.
Drug data last refreshed 4m ago · AI intelligence enriched 6d ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
CERIANNA (Fluoroestradiol F-18) is a positron-emitting radioactive diagnostic agent administered intravenously as a solution. It functions as a radiopharmaceutical for diagnostic imaging, enabling visualization of estrogen receptor activity in patients. The drug targets oncology and neurodegenerative disease imaging where estrogen receptor status is clinically relevant.
Peak
Peak lifecycle positioning indicates stable market presence with established commercial infrastructure; team size likely optimized around core oncology and nuclear medicine segments.
Mechanism of Action
Positron Emitting Activity
Pharmacologic Class:
Radioactive Diagnostic Agent
Indications (1)
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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.