Long-Term Safety of ARQ-154 Foam in Subjects With Seborrheic Dermatitis

Status Completed

Clinical Trial Summary

This is an open-label, long-term safety study of roflumilast ARQ-154 foam 0.3% in subjects with seborrheic dermatitis involving up to 20% total Body Surface Area (BSA). Study was applied topically once daily for 52 weeks. Cohort 1 subjects are rollover subjects from study ARQ-154-203 (NCT04091646) and were rolled into treatment in the current study without interruption. Cohort 2 includes participants from ARQ-154-203 who began treatment in the current study after a gap from completing treatment in the prior study.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04445987
Study type	Interventional
Source	Arcutis Biotherapeutics, Inc.
Contact
Status	Completed
Phase	Phase 2
Start date	June 12, 2020
Completion date	November 19, 2022

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See also
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