NDAINHALATIONPOWDER
Approved
Dec 2013
Lifecycle
Peak
Competitive Pressure
8/100
Data completeness
4/8 — Partial
Drug data last refreshed 20h ago · AI intelligence enriched 3w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
ANORO ELLIPTA is a fixed-dose combination inhaled powder containing umeclidinium bromide (a long-acting muscarinic antagonist) and vilanterol trifenatate (a long-acting beta-2 agonist), approved by the FDA on December 18, 2013. It is indicated for maintenance treatment of chronic obstructive pulmonary disease (COPD), addressing airflow obstruction through dual bronchodilation. The combination represents a standard-of-care maintenance therapy in COPD management, positioning it as a foundational treatment option across disease severity stages.
$0.9BPart D
4.6 years to LOEMechanism 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.
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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.