Laropiprant
DrugOne 100-mg tablet orally once daily for 4 weeks
Other names: MK-0524
NCT Number: NCT01451619
This study will assess the effect of MK-0524 relative to placebo, on signs and symptoms of rosacea and to determine the safety and tolerability profile of MK-0524 in participants with rosacea.
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Notify Me18 year and older
All sexes
Interventional
Phase 1
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
One 100-mg tablet orally once daily for 4 weeks
Other names: MK-0524
One tablet orally once daily for 4 weeks
Time frame: Baseline and Week 4
Time frame: Baseline and Week 4
Merck Sharp & Dohme LLC
Industry
A Randomized, Double-blind, Placebo-controlled, Multi-center, Parallel Group Study to Assess the Pharmacodynamics of MK-0524 in Subjects With Moderate to Severe Erythematotelangiectatic Rosacea. (Protocol No. 155)
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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