A Safety, Efficacy and Systemic Exposure Study of CD5789 Cream in Adults and Adolescents With Lamellar Ichthyosis
Terminated
Mayne Pharma International Pty Ltd
Phase 2
2019-05-01
This is a phase 2 randomized, multi-center, double-blind, vehicle controlled, 90 day, safety,
efficacy, and systemic exposure study followed by a 90 day open-label extension of
trifarotene cream in adults and adolescents with autosomal recessive ichthyosis with lamellar
scale.
A Study to Compare Efficacy and Safety of Trifarotene Cream When Used With an Oral Antibiotic for the Treatment of Severe Acne Vulgaris (AV)
Completed
Galderma R&D
Phase 4
2020-07-28
The purpose of this study is to demonstrate that daily use of topical trifarotene (CD5789) 50
microgram per gram (mcg/g) cream when used in association with oral antibiotic is safe and
effective for the treatment of severe AV.
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