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Extension Study to Evaluate Safety and Efficacy of CTP-543 in Adults With Alopecia Areata

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.

Stanford is currently accepting patients for this trial.

Stanford Investigator(s):

Intervention(s):

  • drug: CTP-543

Eligibility


Inclusion Criteria:

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

Exclusion Criteria:

   - 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

Ages Eligible for Study

18 Years - 65 Years

Genders Eligible for Study

All

Now accepting new patients

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Recruiting