Split-face Study Comparing the Cosmetic Efficacy and Tolerability of Two Topical Products in Participants With Moderate Facial Melasma

Study Identifier
SKM16-LYT-MEL
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
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Study Complete

Results Available

Protocol and Statistical Analysis Plan
Available Language(s): English

Study Details

Medical Condition
  • Dermatology - Other
  • Study Drug
  • 4% Hydroquinone Topical Cream
  • Phase
    N/A
    Sex
    Female & Male
    Age
    18+ years

    Protocol Summary

    The objective of this study is to evaluate the efficacy and tolerability of Lytera 2.0 versus 4% hydroquinone in the improvement of the appearance of moderate facial melasma.

    Study Locations

    Location
    Status
    Location
    Mount Sinai St. Luke's Hospital
    New York, New York, United States, 10025
    Status
    Not applicable