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CompletedNCT03811912

Efficacy and Tolerability Study of Two Dose Regimens of CTP-543 in Adults With Alopecia Areata

A Randomized Parallel-Group Study to Evaluate the Efficacy and Tolerability of Two Dosing Regimens of CTP-543 in Adult Patients With Moderate to Severe Alopecia Areata

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
57 (actual)
Sponsor
Concert Pharmaceuticals · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This study will evaluate the efficacy and tolerability of once-daily versus twice-daily dosing of CTP-543, in adult patients with chronic, moderate to severe alopecia areata.

Conditions

Interventions

TypeNameDescription
DRUGCTP-543CTP-543 administered as 8 mg tablet.
DRUGCTP-543 Matching PlaceboAdministered as tablets to aid treatment masking.

Timeline

Start date
2019-03-21
Primary completion
2019-11-21
Completion
2019-11-21
First posted
2019-01-22
Last updated
2022-12-09
Results posted
2022-12-09

Locations

10 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03811912. Inclusion in this directory is not an endorsement.

Efficacy and Tolerability Study of Two Dose Regimens of CTP-543 in Adults With Alopecia Areata (NCT03811912) · Clinical Trials Directory