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NCT03941548 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by Concert Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
66
Enrollment target

NCT03941548: Completed Phase 2 study, sponsored by Concert Pharmaceuticals.

NCT03941548 is a Phase 2 study that has completed, run by Concert Pharmaceuticals. The registered enrollment target is 66 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (50% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03941548, a Phase 2 study, has completed, sponsored by Concert Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
66 participants
Enrollment target

Study 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.

Primary Outcome

The SALT is a quantitative assessment of scalp hair loss. SALT scores range in severity from 0 (no hair loss) to a maximum of 100 (complete hair loss). Relative change (percent change) to baseline is calculated as: 100 x (\[baseline SALT score - follow-up SALT score\]/baseline SALT score).

Interventions

  • DRUG CTP-543
  • DRUG CTP-543 Matching Placebo

Trial Details

FieldValue
Enrollment Target 66 participants
Start Date 2019-05-24
Est. Completion 2020-04-10
Phase Phase 2
Concert Pharmaceuticals

24 total trials

What the finished NCT03941548 record still lists

NCT03941548 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 66 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (50% lower).

The record links to 0 conditions, and to 2 interventions - of which CTP-543 is the first listed.

NCT03941548 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03941548 about?

NCT03941548 is a clinical study titled "Efficacy and Tolerability Study of Two Dosing Regimens of CTP-543 in Adults With Alopecia Areata". 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.

What is the current status of trial NCT03941548?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 66 participants. The study started on 2019-05-24. Estimated completion is 2020-04-10.

What interventions are being tested in trial NCT03941548?

The interventions under investigation include: CTP-543 (DRUG), CTP-543 Matching Placebo (DRUG).

Who is sponsoring clinical trial NCT03941548?

This trial is sponsored by Concert Pharmaceuticals, which has 24 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03941548's enrollment target sits among peer trials

66 975th of 2000 higher than 1,014 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03941548, the US trial registry maintained by the National Library of Medicine. NCT03941548 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.