drugset / Trial / NCT02833974

Effect of the GSK2245035 on the Allergen-induced Asthmatic Response

NCT02833974

Phase 2 Completed 36 enrolled GlaxoSmithKline
RandomizedParallel-groupDouble-blindTreatment

Summary

This study will assess whether Toll like receptor 7 (TLR7)-mediated pharmacology, with intranasal (i.n.) GSK2245035 20 nanogram (ng) administered weekly for a period of 8 weeks, will lead to reduced allergic reactivity in the lower airways in subjects with mild allergic asthma. This will be a randomised, double-blind (sponsor open), placebo-controlled, parallel group, 8-week treatment study. The study will consist of a screening period of up to approximately 4 weeks (involving two screening visits), a blinded treatment period of 8 weeks, followed by a follow-up period of up to 3 months. The total duration of the study for each subject will therefore be a maximum of approximately 6 months.

Timeline

Start
2016-12-05
Primary completion
2018-02-14
Completion
2018-05-04

Drugs

EvaluationDrugModalityDoseRoute
Subject GSK2245035 Small molecule 20 ng Intranasal

Indications