drugset / Trial / NCT01448902

A Study Of The Effects Of OC000459 In Subjects Known To Suffer From Grass Pollen Induced Allergic Rhinitis

NCT01448902 ↗

Phase 2 Completed 36 enrolled Oxagen Ltd
RandomizedCrossoverDouble-blindTreatment

Summary

The study will assess the efficacy of OC000459 200 mg twice daily orally in comparison to placebo when subjects are challenged in the Vienna Challenge Chamber for 6 hours. This is a randomised, double blind, placebo controlled, two way crossover evaluation. There will be a screening period of up to three weeks and a washout period of at least one week between the two treatment periods. There will be a follow up one to three weeks after the last dose of study drug.

Timeline

Start
2007-03
Primary completion
2007-05
Completion
2007-05

Drugs

EvaluationDrugModalityDoseRoute
Subject TIMAPIPRANT Small molecule 200 mg Oral

Indications