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Clinical Trial Summary

This is a prospective, vehicle controlled, double blinded study to evaluate the safety and potential efficacy of a topical formulation of a MEK inhibitor in patients with erythematotelangiectatic rosacea


Clinical Trial Description

The duration of the study will be 22 days. Subjects will use a cream with a mitogen-activated extracellular signal-regulated kinase (MEK) inhibitor on one cheek, and a cream lacking the inhibitor (vehicle control) on the other. Patients will receive a randomized set of creams for the right and left cheek, one containing the active ingredient. Subjects will be evaluated on days 1, 8, 15 and 22. Skin appearance will be scored in each visit. A blood sample will be obtained to determine the levels of systemic drug absorption. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05616923
Study type Interventional
Source Albany Research Institute, Inc.
Contact
Status Completed
Phase Phase 1
Start date November 1, 2021
Completion date December 31, 2022