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Study to Evaluate the Efficacy and Safety of 1.5 mg/kg/Day of Sarecycline vs Placebo in the Treatment of Acne Vulgaris — SC1401  

Acne Vulgaris Clinical Trial

Official title:
A Randomized, Multicenter, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of 1.5 mg/kg Per Day of Sarecycline Compared to Placebo in the Treatment of Acne Vulgaris

Clinical Trial Summary

A Study to Evaluate the Efficacy and Safety Sarecycline in the Treatment of Acne Vulgaris.

Clinical Trial Description

Treatment of inflammatory lesions of moderate to severe acne vulgaris in subjects 9 to 45 years of age with oral sarecycline 1.5 mg/kg/day compared to placebo in the subjects with moderate to severe facial acne vulgaris based on Investigator's Global Assessment (IGA) score and inflammatory lesion counts. Safety monitored and evaluated throughout 12-week study. ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02651012
Study type Interventional
Source Sadick Research Group
Contact
Status Withdrawn
Phase Phase 3
Start date March 2015
Completion date December 2016
View Details
See also
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