NASONEX
LOE ApproachingNDANASALSPRAY, METERED
Approved
Oct 1997
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Clinical Trials
2
Data completeness
2/8 — Basic
Drug data last refreshed 13h ago · AI intelligence enriched 3w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
NASONEX is a metered nasal spray containing mometasone furoate, a corticosteroid approved for nasal allergic conditions. It delivers anti-inflammatory therapy directly to nasal tissues via intranasal administration. The drug reduces nasal inflammation and allergy symptoms through local glucocorticoid receptor agonism.
LOE Approaching
Brand faces moderate competitive pressure (30/100) and approaching loss of exclusivity; team size likely stable but focused on transition strategy.
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.
Clinical Trials (2)
A Comparison of Patients on AVAMYS ® Versus NASONEX (A Trade Mark of Schering Corporation) and FLIXONASE ® on Key Health Outcome Measures
Started Jul 2009
540 enrolled
Rhinitis, Allergic, Perennial
Nasonex Compared With Placebo in Participants With Seasonal Allergic Rhinitis (SAR) and Concomitant Asthma (P03280)
Started Apr 2003
188 enrolled
Rhinitis, Allergic, SeasonalAsthma
Career Relevance
Working on NASONEX offers limited career expansion in a declining product lifecycle facing imminent generic competition. Roles emphasize defensive market tactics, managed care negotiations, and transition planning rather than growth innovation.
Brand Manager
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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.