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ACTIVE NOT RECRUITING Phase 2

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

NCT03898479 · View on ClinicalTrials.gov ↗

Study 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.

Conditions Studied

Interventions

  • DRUG CTP-543

Study Locations (20)

California

  • Kern Research Inc. — Bakersfield
  • Hope Clinical Research — Canoga Park
  • California Dermatology & Clinical Research Institute — Encinitas
  • University of California, Irvine — Irvine
  • Dermatology Research Associates — Los Angeles
  • Quest Dermatology Research — Northridge
  • Kaiser Permanente Northern California - Oakland — Oakland
  • Palmtree Clinical Research, Inc. — Palm Springs
  • Stanford University School of Medicine - Medical Dermatology Clinic — Redwood City
  • Kaiser Permanente South Sacramento — Sacramento
  • Kaiser Permanente Clinical Trials Unit — San Francisco

Arizona

  • Alliance Dermatology & MOHS Center — Phoenix
  • Center for Dermatology and Plastic Surgery/CCT Research — Scottsdale

Arkansas

  • Johnson Dermatology — Fort Smith
  • Northwest Arkansas Clinical Trials Center, PLLC — Rogers

Colorado

  • Colorado Center for Dermatology, PLLC d/b/a CODerm Research — Centennial
  • Colorado Medical Research Center — Denver

Alabama

  • Total Skin and Beauty Dermatology Center — Birmingham

Connecticut

  • Yale University Church Street Research Unit — New Haven

Florida

  • Skin Care Research, LLC — Boca Raton

Trial Details

FieldValue
Enrollment Target 1,000 participants
Start Date 2019-04-04
Est. Completion 2027-06
Phase Phase 2

Sponsor

Sun Pharmaceutical Industries

20 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03898479

The ClinicalTrials.gov registry entry for NCT03898479 describes a study currently listed as active not recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Sun Pharmaceutical Industries, which has 20 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Alopecia Areata appearing as the primary indexed condition, and to 1 intervention — of which CTP-543 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03898479 reports 20 study locations spanning 7 distinct geographic areas — top geographies include California, Arizona, Arkansas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03898479 about?

NCT03898479 is a clinical study titled "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.

What is the current status of trial NCT03898479?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 1,000 participants. The study started on 2019-04-04. Estimated completion is 2027-06.

What conditions does trial NCT03898479 study?

This clinical trial studies the following conditions: Alopecia Areata. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03898479?

The interventions under investigation include: CTP-543 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03898479?

This trial is sponsored by Sun Pharmaceutical Industries, which has 20 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03898479 being conducted?

This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial