Phase 2 study of RPT193 in adults with atopic dermatitis
Randomized, placebo-controlled Phase 2 study of RPT193 in adults with moderate-to-severe atopic dermatitis
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
229
To Evaluate the Clinical Efficacy of RPT193 Administered Orally Once Daily (QD) for 16 Weeks to Participants With Moderate-to-severe AD
% change in Eczema Area Severity Index (EASI) from baseline at Week 16
Time frame: 16 weeks
Number of Participants With Treatment Emergent Adverse Events (TEAEs)
To evaluate the safety and tolerability of RPT193 administered orally QD for 16 weeks
Time frame: 16 weeks
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Cahaba Dermatology and Skin Health Center
Birmingham, Alabama, United States
Perseverance Research Center
Scottsdale, Arizona, United States
Arkansas Research Trials, LLC
North Little Rock, Arkansas, United States
California Dermatology & Clinical Research Institute
Encinitas, California, United States
First OC Dermatology
Fountain Valley, California, United States
Grimes Center
Los Angeles, California, United States
Dermatology Research Associates
Los Angeles, California, United States
Wallace Medical Group
Los Angeles, California, United States
Velocity Clinical Research
North Hollywood, California, United States
Integrative Skin Science and Research
Sacramento, California, United States
...and 49 more locations