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NCT03495817 · ClinicalTrials.gov registry record · Phase 2

A Study in Male and Female Subjects With Androgenetic Alopecia Treated With ATI-50002 Topical Solution

A Phase 2 study of Androgenetic Alopecia, sponsored by Aclaris Therapeutics.

Completed
Registry status
Phase 2
Development phase
31
Enrollment target
3
Study locations

NCT03495817 is a Phase 2 study of Androgenetic Alopecia that has completed, run by Aclaris Therapeutics. The registered enrollment target is 31 participants, below the 163-participant average among 16 other Androgenetic Alopecia trials with a reported enrollment target (81% lower). The trial reports 3 study locations across 3 states.

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The verdict

NCT03495817, a Phase 2 study of Androgenetic Alopecia, has completed, sponsored by Aclaris Therapeutics.

COMPLETED
Registry status
Phase 2
Development phase
31 participants
Enrollment target
3
Study locations

Study Summary

Open label study to assess safety, tolerability, and efficacy of ATI-50002 in male and female subjects with androgenetic alopecia.

Conditions Studied

Interventions

  • DRUG ATI-50002

Study Locations (3)

Colorado

  • Aclaris Investigational Site - Denver

Oregon

  • Aclaris Investigational Site - Portland

Texas

  • Aclaris Investigational Site - Austin

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2018-03-22
Est. Completion 2019-10-30
Phase Phase 2

Sponsor

Aclaris Therapeutics

33 total trials

What the Registry Record Tells You About NCT03495817

The ClinicalTrials.gov registry entry for NCT03495817 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 31 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 163-participant average among 16 other Androgenetic Alopecia trials with a reported enrollment target (81% lower). The listed sponsor is Aclaris Therapeutics, which has 33 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Androgenetic Alopecia appearing as the primary indexed condition, and to 1 intervention - of which ATI-50002 is the first listed.

NCT03495817 reports 3 study locations spanning 3 distinct geographic areas - top geographies include Colorado, Oregon, Texas.

Frequently Asked Questions

What is clinical trial NCT03495817 about?

NCT03495817 is a clinical study titled "A Study in Male and Female Subjects With Androgenetic Alopecia Treated With ATI-50002 Topical Solution". Open label study to assess safety, tolerability, and efficacy of ATI-50002 in male and female subjects with androgenetic alopecia.

What is the current status of trial NCT03495817?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 31 participants. The study started on 2018-03-22. Estimated completion is 2019-10-30.

What conditions does trial NCT03495817 study?

This clinical trial studies the following conditions: Androgenetic Alopecia.

What interventions are being tested in trial NCT03495817?

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

Who is sponsoring clinical trial NCT03495817?

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

Where is trial NCT03495817 being conducted?

This trial has 3 study locations across Colorado, Oregon, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.