NCT01701024

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

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

• Status: Completed
• Phase: Phase 3
• Study type: Interventional
• Enrollment: 498 (actual)
• Sponsor: Bausch Health Americas, Inc. · Industry
• Sex: All
• Age: 12 Years – 40 Years
• Healthy volunteers: Not accepted

Summary

The primary objective of this study is to compare the efficacy and safety and tolerability of ACYC Gel and vehicle in the treatment of subjects with Acne Vulgaris.

Detailed description

The primary objective of this study is to compare the efficacy and safety and tolerability of ACYC Gel and vehicle in the treatment of subjects with Acne Vulgaris

Conditions

• Acne

Interventions

Type	Name	Description
DRUG	ACYC	ACYC active, topically applied to the face for 12 weeks
DRUG	ACYC vehicle	ACYC vehicle (placebo), topically applied to the face for 12 weeks

Timeline

• Start date: 2012-10-01
• Primary completion: 2013-05-01
• Completion: 2013-07-01
• First posted: 2012-10-04
• Last updated: 2018-06-04
• Results posted: 2017-01-10

Locations

24 sites across 1 country: United States