CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 565 enrolled
Drug / intervention
SCH 39641 6 Amb a 1-U +2 morebiological
Likely dose
Not stated in 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/NCT00783198
NCT00783198Phase 3Completed

A Multicenter, Double-Blind, Randomized, Placebo-Controlled, Parallel-Group Study Evaluating the Efficacy and Long-Term Safety of Ragweed (Ambrosia Artemisiifolia) Sublingual Tablet (SCH 39641) in Adult Subjects With a History of Ragweed-Induced Rhinoconjunctivitis With or Without Asthma

ALK-Abelló A/S·interventional·Posted Oct 31, 2008·Updated Mar 3, 2017

In Brief

A Phase 3 clinical trial evaluating SCH 39641 6 Amb a 1-U, SCH 39641 12 Amb a 1-U, and 1 other intervention for Rhinitis; Allergic, With Asthma and Conjunctivitis. Completed, enrolled 565 participants.

Detailed Summary

This study will evaluate the efficacy and safety of ragweed sublingual tablet (SCH 39641/MK-3641) compared with placebo in participants with ragweed-induced rhinoconjunctivitis over a one-year period. It is expected that ragweed allergic participants on one of the active arms of the trial will have decreased allergic rhinoconjunctivitis symptoms and require less allergy rescue medications during ragweed pollen season.

Study Details

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

Timeline

Phase 3CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedOct 31, 2008
Enrollment StartSep 1, 2009
Primary CompletionMay 1, 2011
TodayJul 2, 2026
Enrollment to primary: 1.7 yearsPosted 17.7 years ago

Interventions

SCH 39641 6 Amb a 1-Ubiological

SCH 39641 6 Amb a 1-U sublingual tablets administered once daily

SCH 39641 12 Amb a 1-Ubiological

SCH 39641 12 Amb a 1-U sublingual tablets administered once daily

Placebobiological

matching placebo sublingual tablets administered once daily