drugset / Trial / NCT01700192

Efficacy and Safety Study of SCH 900237/MK-8237 in Children and Adults With House Dust Mite-Induced Allergic Rhinitis/Rhinoconjunctivitis (P05607)

NCT01700192

Phase 3 Completed 1482 enrolled ALK-Abelló A/S Merck Sharp & Dohme LLC · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to assess the efficacy and safety of MK-8237 (SCH 900237) in the treatment of House Dust Mite (HDM)-Induced Allergic Rhinitis/Rhinoconjunctivitis (AR/ARC) in children and adults. The primary hypothesis of this study is that administration of MK-8237, compared to placebo, results in significant reduction in the average total combined rhinitis score (TCRS).

Timeline

Start
2013-01
Primary completion
2015-04
Completion
2015-04

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject MK-8237 Unknown 12 unknown Other
Background Epinephrine Other / unclassified 0.3 mg Intramuscular
Background Loratadine Small molecule 10 mg Oral
Background Mometasone furoate Other / unclassified 50 ug Intranasal
Background Olopatadine Other / unclassified 0.1 % Other