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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00688064
Other study ID # RD.03.SPR.29074
Secondary ID
Status Completed
Phase Phase 3
First received
Last updated
Start date August 2008
Est. completion date February 2009

Study information

Verified date March 2010
Source Galderma R&D
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to demonstrate the efficacy of Adapalene 0.1% / Benzoyl Peroxide (quoted as BPO) 2.5% Gel associated with Doxycycline Hyclate 100 mg Tablets compared to Adapalene 0.1% /Benzoyl Peroxide 2.5% Vehicle Gel associated with Doxycycline Hyclate 100 mg Tablets, in the treatment of severe acne vulgaris. The safety of the two treatment regimens will also be evaluated.


Description:

Further to this study, eligible Subjects with at least good Global Assessment of Improvement at Week 12 will be randomized in a maintenance study (SPR.29075)


Recruitment information / eligibility

Status Completed
Enrollment 459
Est. completion date February 2009
Est. primary completion date February 2009
Accepts healthy volunteers No
Gender All
Age group 12 Years to 35 Years
Eligibility Inclusion Criteria: - Male or female Subjects of any race, aged 12 to 35 years inclusive - Subjects with severe facial acne (global severity score of 4) - Subjects with a minimum of 20 inflammatory lesions (papules and pustules) on the face, excluding the nose - Subjects with a minimum of 30 and a maximum of 120 non-inflammatory lesions (open comedones and closed comedones) on the face, excluding the nose Exclusion Criteria: - Subjects with more than 3 nodules or cysts on the face, - Subjects with acne conglobata, acne fulminans, secondary acne (chloracne, drug-induced acne, etc.)

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Adapalene BPO Gel associated with Doxycyline Hyclate
Adapalene BPO Gel: Topical to the face, once daily in the evening Doxycycline Hyclate: Oral, 1 tablet once daily in the morning. Both during 12 weeks.
Vehicle Gel associated with Doxycycline Hyclate
Vehicle Gel: Topical to the face, once daily in the evening; Doxycycline Hyclate: Oral, 1 tablet once daily in the morning. Both during 12 weeks.

Locations

Country Name City State
Canada Galderma Investigational Site Barrie Ontario
Canada Galderma Investigational Site North Bay Ontario
Canada Galderma Investigational Site Quebec city Quebec
Canada Galderma Investigational Site Windsor Ontario
Puerto Rico Galderma Investigational Site Aibonito
Puerto Rico Galderma Investigational Site Carolina
United States Galderma Investigational Site Albuquerque New Mexico
United States Galderma Investigational Site Arlington Texas
United States Galderma Investigational Site Austin Texas
United States Galderma Investigational Site Chicago Illinois
United States Galderma Investigational Site College Station Texas
United States Galderma Investigational Site Denver Colorado
United States Galderma Investigational Site Detroit Michigan
United States Galderma Investigational Site Evansville Indiana
United States Galderma Investigational Site Fort Gratiot Michigan
United States Galderma Investigational Site Fridley Minnesota
United States Galderma Investigational Site Hazleton Pennsylvania
United States Galderma Investigational Site Hershey Pennsylvania
United States Galderma Investigational Site Houston Texas
United States Galderma Investigational Site Longmont Colorado
United States Galderma Investigational Site Louisville Kentucky
United States Galderma Investigational Site Lubbock Texas
United States Galderma Investigational Site Miami Florida
United States Galderma Investigational Site Oceanside California
United States Galderma Investigational Site Omaha Nebraska
United States Galderma Investigational Site Overland Park Kansas
United States Galderma Investigational Site San Antonio Texas
United States Galderma Investigational Site San Diego California
United States Galderma Investigational Site Simpsonville South Carolina
United States Galderma Investigational Site Snellville Georgia
United States Galderma Investigational Site Stony Brook New York
United States Galderma Investigational Site Warren Ohio
United States Galderma Investigational Site Webster Texas
United States Galderma Investigational Site Winston-Salem North Carolina

Sponsors (1)

Lead Sponsor Collaborator
Galderma R&D

Countries where clinical trial is conducted

United States,  Canada,  Puerto Rico, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percent Change From Baseline in Total Lesion Counts at Week 12. Week 12
Secondary Percent Change From Baseline in Inflammatory Lesion Counts at Week 12. Week 12
Secondary Percent Change From Baseline in Non-inflammatory Lesion Counts at Week 12 Week 12
Secondary Success Rate on the Investigator's Global Assessment Percentage of subjects graded "Clear" or "Almost Clear" on 6-point IGA scale(0=clear, 1=almost clear, 2=mild, 3=moderate, 4=severe and 5=very severe)at week 12 Week 12
Secondary Percent of Subjects With Adverse Events Percent of subjects with Adverse Events all along the study (up to 12 weeks follow-up period) Up to 12 weeks

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