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NCT03315689 · ClinicalTrials.gov registry record · Phase 2

Safety and Pharmacokinetic Study of ATI-50002 in Subjects With Alopecia Universalis (AU) and Alopecia Totalis (AT)

A Phase 2 study, sponsored by Aclaris Therapeutics.

Completed
Registry status
Phase 2
Development phase
11
Enrollment target

NCT03315689: Completed Phase 2 study, sponsored by Aclaris Therapeutics.

NCT03315689 is a Phase 2 study that has completed, run by Aclaris Therapeutics. The registered enrollment target is 11 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03315689, a Phase 2 study, has completed, sponsored by Aclaris Therapeutics.

COMPLETED
Registry status
Phase 2
Development phase
11 participants
Enrollment target

Study Summary

The primary objective is to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of ATI-50002 Topical Solution compared to vehicle in subjects with AU and AT.

Primary Outcome

ATI-50002 levels in scalp biopsies taken at Visits 3 (Day 2) and 7 (Day 29).

Interventions

  • DRUG Vehicle
  • DRUG ATI-50002

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2017-12-14
Est. Completion 2019-06-20
Phase Phase 2
Aclaris Therapeutics

33 total trials

What the finished NCT03315689 record still lists

NCT03315689 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 11 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower).

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

NCT03315689 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03315689 about?

NCT03315689 is a clinical study titled "Safety and Pharmacokinetic Study of ATI-50002 in Subjects With Alopecia Universalis (AU) and Alopecia Totalis (AT)". The primary objective is to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of ATI-50002 Topical Solution compared to vehicle in subjects with AU and AT.

What is the current status of trial NCT03315689?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 11 participants. The study started on 2017-12-14. Estimated completion is 2019-06-20.

What interventions are being tested in trial NCT03315689?

The interventions under investigation include: Vehicle (DRUG), ATI-50002 (DRUG).

Who is sponsoring clinical trial NCT03315689?

This trial is sponsored by Aclaris Therapeutics, which has 33 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03315689's enrollment target sits among peer trials

11 1967th of 2000 higher than 33 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 NCT03315689, the US trial registry maintained by the National Library of Medicine. NCT03315689 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.