NDAINHALATIONPOWDER
Approved
Sep 2017
Lifecycle
Peak
Competitive Pressure
0/100
Clinical Trials
1
Data completeness
4/8 — Partial
Drug data last refreshed Yesterday · AI intelligence enriched 3w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
TRELEGY ELLIPTA is a triple-combination inhaled powder containing fluticasone furoate (inhaled corticosteroid), umeclidinium bromide (long-acting anticholinergic), and vilanterol trifenatate (long-acting beta-2 agonist) approved by the FDA on September 18, 2017. It is indicated for maintenance treatment of chronic obstructive pulmonary disease (COPD) in patients where combination therapy is appropriate. The product combines three distinct pharmacologic mechanisms to reduce airway obstruction and inflammation in a single inhaler device. TRELEGY ELLIPTA represents a convenient once-daily maintenance option for moderate-to-severe COPD patients.
$4.5BPart D
4.9 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.
Clinical Trials (1)
To Evaluate Real-World Effectiveness of Fluticasone Furoate/Umeclidinium Bromide/Vilanterol (FF/UMEC/VI) in a Single Inhaler (Trelegy Ellipta) in Participants With Symptomatic COPD
Started Oct 2022
463 enrolled
Pulmonary Disease, Chronic Obstructive
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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.