NDAINTRAVENOUSINJECTABLE
Approved
Aug 2004
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Clinical Trials
1
Data completeness
3/8 — Basic
FLUDEOXYGLUCOSE F18 (fludeoxyglucose f-18) by Medica Corp is radiopharmaceutical activity [moa]. First approved in 2004.
Drug data last refreshed 16h ago · AI intelligence enriched 1mo ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
Fludeoxyglucose F-18 is a radiopharmaceutical glucose analog labeled with fluorine-18 that localizes to tissues with increased metabolic activity. It is administered intravenously for positron emission tomography (PET) imaging to detect cancer, cardiac viability, and neurological disorders. The mechanism relies on radiolabeled glucose uptake in metabolically active cells, enabling functional and molecular imaging.
LOE Approaching
With LOE approaching, commercial teams are likely consolidating and shifting focus toward lifecycle extension or next-generation imaging agents.
Mechanism of Action
Radiopharmaceutical Activity
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (1)
Fludeoxyglucose F-18-PET in Planning Lung Cancer Radiation Therapy
Started Apr 2018
19 enrolled
Stage I Lung CancerStage I Non-Small Cell Lung Cancer AJCC v7Stage IA Non-Small Cell Lung Carcinoma AJCC v7+5 more
Career Relevance
Working on Fludeoxyglucose F-18 offers specialized expertise in radiopharmaceutical development, manufacturing, and regulatory compliance—valuable for diagnostic imaging or nuclear medicine careers. However, with LOE approaching and zero linked open positions, career growth opportunities are constrained; professionals should expect roles focused on cost optimization, market maintenance, and regulatory defense rather than commercial expansion.
Diagnostic Imaging Specialist
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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.