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Completed Phase 2 Interventional Results available

Treatment of Moderate to Severe Facial Acne Vulgaris

ClinicalTrials.gov ID: NCT00612573

Public ClinicalTrials.gov record NCT00612573. 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 Jul 22, 2026, 9:09 AM EDT

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

Official title

Phase 2 Study Randomized, Double-blind Study to Evaluate the Safety and Efficacy of 3 Doses of Doxycycline as Compared to Placebo in the Treatment of Moderate to Severe Facial Acne Vulgaris

Study identification

NCT ID
NCT00612573
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Warner Chilcott
Industry
Enrollment
257 participants

Conditions and interventions

Conditions

Interventions

  • Doxycycline 0.6 mg/kg/day Drug
  • Doxycycline 1.2 mg/kg/day Drug
  • Doxycycline 2.4 mg/kg/day Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
12 Years to 45 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
Jan 31, 2008
Primary completion
Oct 31, 2008
Completion
Nov 30, 2008
Last update posted
Apr 21, 2013

2008

United States locations

U.S. sites
23
U.S. states
14
U.S. cities
23
Facility City State ZIP Site status
Warner Chilcott Investigational Site Encino California 91436
Warner Chilcott Investigational Site Fremont California 94538
Warner Chilcott Investigational Site Los Angeles California 90045
Warner Chilcott Investigational Site Sacramento California 95816
Warner Chilcott Investigational Site Denver Colorado 80210
Warner Chilcott Investigational Site Miami Florida 33175
Warner Chilcott Investigational Site Newnan Georgia 30263
Warner Chilcott Investigational Site Snellville Georgia 30078
Warner Chilcott Investigational Site Louisville Kentucky 40217
Warner Chilcott Investigational Site Clinton Township Michigan 48038
Warner Chilcott Investigational Site Albuquerque New Mexico 87106-5239
Warner Chilcott Investigational Site Rochester New York 14623
Warner Chilcott Investigational Site Winston-Salem North Carolina 27103
Warner Chilcott Investigational Site Cincinnati Ohio 45219
Warner Chilcott Investigational Site Portland Oregon 97210
Warner Chilcott Investigational Site Broomall Pennsylvania 19008
Warner Chilcott Investigational Site Fort Washington Pennsylvania 19034
Warner Chilcott Investigational Site Austin Texas 78759
Warner Chilcott Investigational Site College Station Texas 77845
Warner Chilcott Investigational Site Dallas Texas 75246
Warner Chilcott Investigational Site Houston Texas 77056
Warner Chilcott Investigational Site San Antonio Texas 78229
Warner Chilcott Investigational Site Spokane Washington 99204

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 NCT00612573, 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 Apr 21, 2013 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00612573 live on ClinicalTrials.gov.

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