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NCT04487860 · ClinicalTrials.gov registry record · Phase 2

Efficacy and Safety of AS012 in Subjects With Non-segmental Vitiligo

A Phase 2 study of Non-segmental Vitiligo, sponsored by Ache Laboratorios Farmaceuticos S.A..

Completed
Registry status
Phase 2
Development phase
327
Enrollment target
20
Study locations

NCT04487860 is a Phase 2 study of Non-segmental Vitiligo that has completed, run by Ache Laboratorios Farmaceuticos S.A.. The registered enrollment target is 327 participants, above the 161-participant average among 5 other Non-segmental Vitiligo trials with a reported enrollment target (103% higher). The trial reports 20 study locations across 12 states.

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The verdict

NCT04487860, a Phase 2 study of Non-segmental Vitiligo, has completed, sponsored by Ache Laboratorios Farmaceuticos S.A..

COMPLETED
Registry status
Phase 2
Development phase
327 participants
Enrollment target
20
Study locations

Study Summary

This is a randomized, double blind, placebo-controlled, phase II study. The study will be performed as a multicenter, multinational study.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG AS012

Study Locations (20)

Florida

  • Sun Pharma Site 01 - Brandon
  • Sun Pharma Site 06 - Fort Lauderdale
  • Sun Pharma Site 04 - Miami
  • Sun Pharma Site 05 - Miramar
  • Sun Pharma Site 10 - Ormond Beach

California

  • Sun Pharma Site 09 - Fremont
  • Sun pharma site 30 - Los Angeles

Louisiana

  • Sun Pharma Site 12 - Baton Rouge
  • Sun Pharma Site 13 - New Orleans

Rhode Island

  • Sun Pharma Site 29 - East Greenwich
  • Sun Pharma Site 08 - Warwick

Texas

  • Sun Pharma Site 03 - Dallas
  • Sun Pharma Site 16 - Pflugerville

Arizona

  • Sun Pharma Site 15 - Phoenix

Arkansas

  • Sun Pharma Site 02 - Bryant

Indiana

  • Sun Pharma Site 14 - West Lafayette

Trial Details

FieldValue
Enrollment Target 327 participants
Start Date 2021-01-13
Est. Completion 2023-02-27
Phase Phase 2

What the Registry Record Tells You About NCT04487860

The ClinicalTrials.gov registry entry for NCT04487860 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 327 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 161-participant average among 5 other Non-segmental Vitiligo trials with a reported enrollment target (103% higher). The listed sponsor is Ache Laboratorios Farmaceuticos S.A., which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Non-segmental Vitiligo appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT04487860 reports 20 study locations spanning 12 distinct geographic areas - top geographies include Florida, California, Louisiana.

Frequently Asked Questions

What is clinical trial NCT04487860 about?

NCT04487860 is a clinical study titled "Efficacy and Safety of AS012 in Subjects With Non-segmental Vitiligo". This is a randomized, double blind, placebo-controlled, phase II study. The study will be performed as a multicenter, multinational study.

What is the current status of trial NCT04487860?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 327 participants. The study started on 2021-01-13. Estimated completion is 2023-02-27.

What conditions does trial NCT04487860 study?

This clinical trial studies the following conditions: Non-segmental Vitiligo.

What interventions are being tested in trial NCT04487860?

The interventions under investigation include: Placebo (DRUG), AS012 (DRUG).

Who is sponsoring clinical trial NCT04487860?

This trial is sponsored by Ache Laboratorios Farmaceuticos S.A., which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04487860 being conducted?

This trial has 20 study locations across Arizona, Arkansas, California, Florida, Indiana. 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

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