Condition: Atopic Dermatitis (AD) · Eczema · Sponsor: Arcutis Biotherapeutics, Inc.
This is a first-in-human, Phase 1, double-blind, randomized, placebo-controlled, dose-escalation study evaluating ARQ-234. The study is designed to assess the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of ARQ-234 in two populations: healthy volunteers and participants with moderate to severe atopic dermatitis (AD). Healthy volunteers will participate in Single Ascending Dose (SAD) Cohorts 1-5. Participants with moderate to severe AD will be enrolled in SAD Cohorts 6-7, Multiple Ascending Dose (MAD) Cohorts, and a Proof-of-Concept (POC) expansion cohort.
This description comes directly from the study's public registry record.
Arcutis Medical Information · 1-844-692-6729 · medinfo@arcutis.com
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| Clinical Site 101 | Fair Lawn, New Jersey, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07453602