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Completed Phase 3 Interventional Results available

Clinical Study to Test the Efficacy and Safety of ACYC to Treat Moderate to Severe Acne

ClinicalTrials.gov ID: NCT01701024

Public ClinicalTrials.gov record NCT01701024. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jun 26, 2026, 12:58 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Multi-Center, Randomized, Double-Blind, Vehicle-Controlled, 2-Arm, Parallel Group Comparison Study Comparing the Efficacy and Safety of ACYC and ACYC Vehicle Gel in the Treatment of Acne Vulgaris

Study identification

NCT ID
NCT01701024
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bausch Health Americas, Inc.
Industry
Enrollment
498 participants

Conditions and interventions

Conditions

Interventions

  • ACYC Drug
  • ACYC vehicle Drug

Drug

Eligibility (public fields only)

Age range
12 Years to 40 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 30, 2012
Primary completion
Apr 30, 2013
Completion
Jun 30, 2013
Last update posted
Jun 3, 2018

2012 – 2013

United States locations

U.S. sites
24
U.S. states
18
U.S. cities
24
Facility City State ZIP Site status
Not listed Mobile Alabama 36608
Not listed Los Angeles California 90045
Not listed San Diego California 92123
Not listed New Haven Connecticut 06511
Not listed Aventura Florida 33180
Not listed Naperville Illinois 60563
Not listed Evansville Indiana 47714
Not listed South Bend Indiana 46617
Not listed Louisville Kentucky 40202
Not listed Clinton Township Michigan 48038
Not listed Fridley Minnesota 55432
Not listed Omaha Nebraska 68144
Not listed Albuquerque New Mexico 87106
Not listed Rochester New York 14623
Not listed Raleigh North Carolina 27612
Not listed Portland Oregon 97210
Not listed Goodlettsville Tennessee 37072
Not listed Austin Texas 78759
Not listed College Station Texas 77845
Not listed Houston Texas 77056
Not listed San Antonio Texas 78250
Not listed Salt Lake City Utah 84117
Not listed Lynchburg Virginia 24501
Not listed Norfolk Virginia 23507

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01701024, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 3, 2018 · Synced Jun 26, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01701024 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →