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Clinical Trial Summary

The purpose of this study is to evaluate the safety of two doses (6 Development Units [DU] and 12 DU) of MK-8237 sublingual tablets compared to Placebo in adolescents with house dust mite-induced allergic rhinitis/rhinoconjunctivitis. The primary hypothesis is that at least one dose of MK-8237 sublingual tablet is safe and well-tolerated in adolescents with house dust mite-induced allergic rhinitis/rhinoconjunctivitis.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01678807
Study type Interventional
Source ALK-Abelló A/S
Contact
Status Completed
Phase Phase 1
Start date October 2012
Completion date May 2013

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