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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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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Laropiprant | Experimental |
| |
| Placebo | Placebo Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Laropiprant | Drug | One 100-mg tablet orally once daily for 4 weeks |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in Clinician's Erythema Assessment (CEA) Scale Score from Baseline | Baseline and Week 4 |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Patient Self Assessment (PSA) Score from Baseline | Baseline and Week 4 |
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Inclusion Criteria:
Exclusion Criteria:
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| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 25142778 | Result | Krishna R, Guo Y, Schulz V, Cord-Cruz E, Smith S, Hair S, Nahm WK, Draelos ZD. Non-obligatory role of prostaglandin D2 receptor subtype 1 in rosacea: laropiprant in comparison to a placebo did not alleviate the symptoms of erythematoelangiectaic rosacea. J Clin Pharmacol. 2015 Feb;55(2):137-43. doi: 10.1002/jcph.383. Epub 2014 Sep 4. |
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| ID | Term |
|---|---|
| D012393 | Rosacea |
| ID | Term |
|---|---|
| D012871 | Skin Diseases |
| D017437 | Skin and Connective Tissue Diseases |
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| ID | Term |
|---|---|
| C518174 | MK-0524 |
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| Placebo for Laropiprant | Drug | One tablet orally once daily for 4 weeks |
|