BYDUREON BCISE
PeakNDASUBCUTANEOUSSUSPENSION, EXTENDED RELEASE
Approved
Oct 2017
Lifecycle
Peak
Competitive Pressure
8/100
Data completeness
3/8 — Basic
Drug data last refreshed 9h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
BYDUREON BCISE is an extended-release subcutaneous suspension approved by the FDA in October 2017 for diabetes management. It is a small-molecule GLP-1 receptor agonist delivered via injection, designed for once-weekly dosing to improve glycemic control. The product represents an advancement in formulation technology for chronic metabolic disease management.
$284MPart D
Peak4.5 years to LOEAt peak lifecycle with $284M annual Part D spending, the brand supports a mature, specialized commercial infrastructure focused on optimization and patient retention.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Why This Matters for Your Career
LOE in ~5 years — strategic planning for patent cliff underway
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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.