At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
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
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
Timeline
Interventions
SCH 39641 6 Amb a 1-U sublingual tablets administered once daily
SCH 39641 12 Amb a 1-U sublingual tablets administered once daily
matching placebo sublingual tablets administered once daily