Drug intelligence / Profile preview

pranlukast

Development stage
Phase 3
Lead developer
Ono Pharmaceutical
Modality
Small Molecules
Administration
Oral
01

Overview

Pranlukast is a small molecule leukotriene receptor antagonist primarily used for the prevention and treatment of bronchial asthma and allergic rhinitis. It acts by selectively antagonizing the cysteinyl leukotriene receptor 1 (CysLT1), thereby inhibiting the action of leukotriene D4 (LTD4). This prevents airway edema, smooth muscle contraction, and excessive mucus secretion in response to allergens. Pranlukast is typically used as an adjunct to inhaled corticosteroids and beta agonists in asthma management. It was first developed by Ono Pharmaceutical in Japan, where it has been widely marketed since its approval in 1995[1][2][3][4][5].

Brand names
OnonAzlaire
Other names
Pranlukast hydrateN-[4-oxo-2-(2H-tetrazol–5–yl)chromen–8–yl]–4-(4–phenylbutoxy)benzamide
02

Targets

CYSLTR1 (Cysteinyl-leukotriene type 1 receptor)

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