Drug intelligence / Profile preview

azelastine + fluticasone

Development stage
Phase 4
Lead developer
Meda
Modality
Small Molecules
Administration
Intranasal
01

Overview

**Azelastine + fluticasone** is a fixed-dose intranasal combination of azelastine hydrochloride, a histamine H1-receptor antagonist, and fluticasone propionate, a synthetic glucocorticoid corticosteroid. It was developed as MP29-02 and marketed as Dymista, delivering 137 mcg azelastine hydrochloride and 50 mcg fluticasone propionate per spray in the US formulation. The combination provides rapid antihistamine-mediated control of histamine-driven nasal symptoms alongside glucocorticoid receptor-mediated suppression of allergic nasal inflammation. It is approved for symptomatic treatment of seasonal allergic rhinitis in adults and pediatric patients aged 6 years and older in the United States, with allergic rhinitis and perennial allergic rhinitis indications in other markets. ([accessdata.fda.gov](https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/202236s021lbl.pdf))

Brand names
Dymista
Other names
AzeFluazelastine hydrochloride + fluticasone propionateazelastine hydrochloride and fluticasone propionateazelastine/fluticasonefluticasone + azelastinefluticasone propionate + azelastine hydrochlorideMP-AzeFlu
02

Targets

GR (Glucocorticoid receptor)HRH1 (Histamine H1 Receptor)

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