Drug intelligence / Profile preview

olopatadine + fluticasone propionate

Development stage
Preclinical
Lead developer
Glenmark Pharmaceuticals
Modality
Small Molecules
Administration
Intranasal
01

Overview

A combination of **olopatadine** (an H1-receptor antagonist/antihistamine) and **fluticasone propionate** (a synthetic glucocorticoid corticosteroid) used as a topical (generally intranasal) therapy for the symptomatic relief of **allergic rhinitis** and allergic rhinoconjunctivitis. **Olopatadine** blocks the activity of histamine at H1 receptors, alleviating symptoms such as sneezing, nasal pruritus, and rhinorrhea. **Fluticasone propionate** acts as an anti-inflammatory agent, reducing inflammation by affecting the production and activity of a range of inflammatory cells and mediators, including mast cells, eosinophils, neutrophils, macrophages, lymphocytes, histamine, eicosanoids, leukotrienes, and cytokines[1][2][3]. The combination is intended to provide both rapid antihistaminic effects and broad anti-inflammatory action for nasal and/or ocular allergic symptoms. Currently, the most widely marketed fixed-dose antihistamine/intranasal steroid combinations use **azelastine** rather than olopatadine, and there does not appear to be an FDA-approved fixed product of olopatadine + fluticasone propionate, though both are sometimes used concomitantly in practice or in clinical studies.

02

Targets

HRH1 (Histamine H1 Receptor)Ca signaling (Calcium signaling family)GR (Glucocorticoid receptor)HRH2 (Histamine H2 Receptor)HRH3 (Histamine Receptor H3)

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