Topical Crisaborole in Patients With Alopecia Areata

Status Withdrawn

Clinical Trial Summary

The aim of this study is to determine whether topical crisaborole improves hair growth in alopecia areata.

Clinical Trial Description

Each individual will be enrolled in the study for 24 weeks. Following a 28 days screening period, eligible subjects will be randomized in a 1:1 ratio to receive either crisaborole 2% ointment or matching placebo for 12 weeks. The primary endpoint is assessed at week 12. At the week 12 visit, all subjects will enter the open label treatment period where they will all receive crisaborole 2% ointment for an additional 12 weeks, with the last study visit taking place on week 24. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04299503
Study type	Interventional
Source	Tufts Medical Center
Contact
Status	Withdrawn
Phase	Phase 2
Start date	March 6, 2020
Completion date	December 2022

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See also
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