Drug intelligence / Profile preview

loratadine + placebo

Development stage
Unknown
Lead developer
Merck
Modality
Small Molecules
Administration
Oral, Intranasal
01

Overview

Loratadine + placebo refers to a specific clinical trial intervention arm, primarily associated with studies conducted by Bayer to evaluate the efficacy and onset of action of antihistamines in seasonal allergic rhinitis. This regimen typically involves the oral administration of a 10 mg loratadine tablet alongside a placebo nasal spray, a design used to maintain double-blinding in trials comparing oral medications with intranasal therapies like azelastine. Loratadine is a second-generation, non-sedating H1-antihistamine that works as a selective peripheral histamine H1-receptor antagonist. It is indicated for the relief of symptoms such as sneezing, runny nose, and itchy eyes or throat. By blocking the action of histamine, a primary mediator of the allergic response, loratadine effectively manages the inflammatory symptoms of hay fever and other upper respiratory allergies.

Other names
loratadine and placebo
02

Targets

HRH1 (Histamine H1 Receptor)

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