Summary

Eligibility
for people ages 18-65 (full criteria)
Location
at UC Irvine
Dates
study started
completion around

Description

Summary

The overall objectives of the study are to evaluate long-term safety of CTP-543 and to assess long-term effects of CTP-543 on treating hair loss in adult patients with chronic, moderate to severe alopecia areata.

Official Title

A Multicenter, Open-Label, Extension Study to Assess the Long-Term Safety and Efficacy of CTP-543 in Adult Patients With Moderate to Severe Alopecia Areata

Keywords

Alopecia Areata, Alopecia, CTP-543

Eligibility

You can join if…

Open to people ages 18-65

  • Have completed 24 weeks of treatment in a previous qualifying CTP-543 clinical trial

You CAN'T join if...

  • Active scalp inflammation, psoriasis, or seborrheic dermatitis requiring topical treatment to the scalp, significant trauma to the scalp, or untreated actinic keratosis
  • Females who are nursing, pregnant, or planning to become pregnant while in the study, and for 30 days after last dose of study medication
  • Donation of blood at any point throughout the study and for 30 days after last dose of study medication

Locations

  • University of California, Irvine
    Irvine California 92697 United States
  • Kaiser Permanente Clinical Trials Unit
    San Francisco California 94118 United States
  • Dermatology Research Associates
    Los Angeles California 90045 United States
  • Hope Clinical Research
    Canoga Park California 91303 United States
  • California Dermatology & Clinical Research Institute
    Encinitas California 92024 United States
  • Quest Dermatology Research
    Northridge California 91324 United States
  • Kaiser Permanente Northern California - Oakland
    Oakland California 94611 United States
  • Kaiser Permanente South Sacramento
    Sacramento California 95823 United States
  • Stanford University School of Medicine - Medical Dermatology Clinic
    Redwood City California 94063 United States

Details

Status
in progress, not accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Concert Pharmaceuticals
ID
NCT03898479
Phase
Phase 2/3 Alopecia Research Study
Study Type
Interventional
Participants
Expecting 1000 study participants
Last Updated