CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 53 enrolled
Drug / intervention
JNJ-39220675 +2 moredrug
Likely dose
JNJ-39220675 1 mlfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00804687
NCT00804687Phase 2Completed

A Randomized, Single-Dose, Single-Blind, Double-Dummy, Placebo-Controlled, Three-Way Cross-Over Study to Compare the Relative Efficacy of JNJ-39220675, Pseudoephedrine and Placebo for the Treatment of Allergic Rhinitis in an Environmental Exposure Chamber (EEC) Model

Johnson & Johnson Pharmaceutical Research & Development, L.L.C.·interventional·Posted Dec 9, 2008·Updated Oct 30, 2013

In Brief

A Phase 2 clinical trial evaluating Placebo, JNJ-39220675, and 1 other intervention for Allergic Rhinitis. Completed, enrolled 53 participants across 1 site.

Detailed Summary

The purpose of this study is to evaluate the relative efficacy of JNJ- 39220675 and pseudoephedrine compared to placebo (medication with no active ingredients) in participants with allergic rhinitis (inflammation of the nose due to exposure to allergens such as pollen, dust or animal hair).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada
Collaborators--

Timeline

Phase 2CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedDec 9, 2008
Enrollment StartNov 1, 2008
Primary CompletionFeb 1, 2009
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 17.6 years ago

Interventions

Placeboother

Single-dose of 1 milliliter (ml) placebo solution will be administered orally and/or placebo tablet orally in one of the treatment periods.

JNJ-39220675drug

Single-dose of JNJ-39220675 will be administered as 1 ml of 10 milligram/milliliter solution orally in one of the treatment periods.

Pseudoephedrinedrug

Single-dose of 60 milligram pseudoephedrine tablet will be administered orally in one of the treatment periods.