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A Extension Study to Evaluate Safety and Efficacy of CTP-543 in Adults With Alopecia Areata.
Overall Recruitment Status: Active, currently enrolling
 
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.
 
Region Sponsors
California - Northern
Concert Pharmaceuticals
 
Acronym KP IRB No.
CTP-543 1405545
 
Study Type Phase
Clinical Trial Phase II
 
Study Population Description
(Adult, Older Adult) Male and Female with Alopecia Areata.
 
Purpose
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.
 
Detailed Description
 
Gender Age Limit
Male & Female 18 - 65 years
 
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

 
Keywords and/or Specific Medical Conditions
  • Alopecia
  • Pathological Conditions, Anatomical
  • Alopecia Areata
  • Pathology
  • CP543.5001
  • Skin Diseases
  • Hair Diseases
  • Dermatology
  • Hypotrichosis
 
KP Clinical Facility
  • San Francisco Medical Center
 
Clinical Area
  • Dermatology
  • Pathology


Principal Investigator:
Paradi Mirmirani, MD
Contact Information:
- Daisy Mendoza-Zepeda
-Central Valley-Manteca


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