Healthy Volunteers Clinical Trial
Official title:
A Phase 1, 21-Day, Randomized, Evaluator Blinded, Controlled Study to Evaluate the Irritation Potential of M518101 in Healthy Volunteers, Using a Cumulative Irritant Patch Test Design
This is a single center, randomized, controlled, within-subject comparison, multiple dose
study to determine the irritation potential of M518101 on normal skin under occlusive patch
condition.
The study drug will be applied for 21 days under occlusive patch condition. The irritation
potential of M518101 will be compared with positive, negative control and M518101 vehicle.
The study duration is 21days and there will be at least 23 visits to study center including
screening visit.
n/a
Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Outcomes Assessor)
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