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This study investigates the safety and efficacy of MBI 226 2.5% and 5.0% Acne Solutions, applied topically for six weeks, in the treatment of acne.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| MBI 226 Acne Solutions | Drug |
| Measure | Description | Time Frame |
|---|---|---|
| - percent change in inflammatory, non-inflammatory, and total acne lesion counts over entire study and dichotomized Global Severity Assessment |
| Measure | Description | Time Frame |
|---|---|---|
| - percent change in lesion counts after ~2 and ~4 weeks | ||
| - Global Severity Assessment |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Jim Pankovich | BioWest Therapeutics Inc | Study Director |
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| ID | Term |
|---|---|
| D000152 | Acne Vulgaris |
| ID | Term |
|---|---|
| D017486 | Acneiform Eruptions |
| D012871 | Skin Diseases |
| D017437 | Skin and Connective Tissue Diseases |
| D012625 | Sebaceous Gland Diseases |
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