Differin® Gel x12 Wks vs Tazorac® Cream x12 Wks vs Differin® x6 Wks Switched to Tazorac® x6 Wks for Treatment of Acne
Primary Purpose
Acne Vulgaris
Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Adapalene Gel, 0.1%
Tazarotene Cream, 0.1%
Adapalene Gel, 0.1% + Tazarotene Cream, 0.1%
Sponsored by
About this trial
This is an interventional treatment trial for Acne Vulgaris
Eligibility Criteria
Inclusion Criteria:
- Subjects with a minimum of 20 inflammatory lesions (papules and pustules) on the face
- Subjects with a minimum of 15 and a maximum of 100 non-inflammatory lesions (open comedones and closed comedones) on the face, excluding the nose
Exclusion Criteria:
- Subjects with more than 3 nodulo-cystic lesions
Sites / Locations
- Therapeutics Clinical Research
- Henry Ford Medical Center-Dept. of Dermatology
- Minnesota Clinical Study Center
- State University of New York Downstate Medical Center-Dept. of Dermatology
- Dermatology Research Associates
- Phoebe Rich, MD & Associates
- Milton S. Hershey Medical Center Center-Div. of Dermatology
- DermResearch, Inc.
- J & S Studies, Inc.
- Stephens & Associates
- Dermatology Research Center
- Virginia Clinical Research, Inc.
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Active Comparator
Arm Label
1
2
3
Arm Description
Differin® Gel, 0.1% for 12 weeks
Tazorac® Cream, 0.1% for 12 weeks
Differin® Gel, 0.1% for 6 weeks switched to Tazorac® Cream, 0.1% for 6 weeks
Outcomes
Primary Outcome Measures
Efficacy - total lesion counts
Secondary Outcome Measures
Safety - tolerability assessments and adverse event reporting
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00469755
Brief Title
Differin® Gel x12 Wks vs Tazorac® Cream x12 Wks vs Differin® x6 Wks Switched to Tazorac® x6 Wks for Treatment of Acne
Official Title
A Comparison of Differin® Gel, 0.1% vs. Tazorac® Cream, 0.1% vs. Differin® Gel, 0.1% 6-week Treatment Switched to Tazorac® Cream, 0.1% 6-week Treatment in Patients With Acne Vulgaris
Study Type
Interventional
2. Study Status
Record Verification Date
March 2008
Overall Recruitment Status
Completed
Study Start Date
February 2006 (undefined)
Primary Completion Date
September 2006 (Actual)
Study Completion Date
September 2006 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Galderma R&D
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
To determine the efficacy and safety of 12 weeks of treatment with Differin Gel, 0.1% compared to 12 weeks of treatment with Tazorac Cream, 0.1% and compared to 6 weeks treatment with Differin Gel, 0.1% followed by 6 weeks of treatment with Tazorac Cream
Detailed Description
Same as above.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acne Vulgaris
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Factorial Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
302 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Active Comparator
Arm Description
Differin® Gel, 0.1% for 12 weeks
Arm Title
2
Arm Type
Active Comparator
Arm Description
Tazorac® Cream, 0.1% for 12 weeks
Arm Title
3
Arm Type
Active Comparator
Arm Description
Differin® Gel, 0.1% for 6 weeks switched to Tazorac® Cream, 0.1% for 6 weeks
Intervention Type
Drug
Intervention Name(s)
Adapalene Gel, 0.1%
Other Intervention Name(s)
Differin® Gel, 0.1%
Intervention Description
Apply once daily in the evening for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Tazarotene Cream, 0.1%
Other Intervention Name(s)
Tazorac® Cream, 0.1%
Intervention Description
Apply once daily in the evening for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Adapalene Gel, 0.1% + Tazarotene Cream, 0.1%
Other Intervention Name(s)
Differin® Gel, 0.1% and Tazorac® Cream, 0.1%
Intervention Description
Apply adapalene Gel, 0.1% once daily in the evening for 6 weeks and Tazarotene Cream, 0.1% once daily in the evening for 6 weeks
Primary Outcome Measure Information:
Title
Efficacy - total lesion counts
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Safety - tolerability assessments and adverse event reporting
Time Frame
12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Subjects with a minimum of 20 inflammatory lesions (papules and pustules) on the face
Subjects with a minimum of 15 and a maximum of 100 non-inflammatory lesions (open comedones and closed comedones) on the face, excluding the nose
Exclusion Criteria:
Subjects with more than 3 nodulo-cystic lesions
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ronald W Gottschalk, MD
Organizational Affiliation
Galderma R&D
Official's Role
Study Director
Facility Information:
Facility Name
Therapeutics Clinical Research
City
San Diego
State/Province
California
ZIP/Postal Code
92123
Country
United States
Facility Name
Henry Ford Medical Center-Dept. of Dermatology
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48202
Country
United States
Facility Name
Minnesota Clinical Study Center
City
Fridley
State/Province
Minnesota
ZIP/Postal Code
55432
Country
United States
Facility Name
State University of New York Downstate Medical Center-Dept. of Dermatology
City
Brooklyn
State/Province
New York
ZIP/Postal Code
11203
Country
United States
Facility Name
Dermatology Research Associates
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45230
Country
United States
Facility Name
Phoebe Rich, MD & Associates
City
Portland
State/Province
Oregon
ZIP/Postal Code
97210
Country
United States
Facility Name
Milton S. Hershey Medical Center Center-Div. of Dermatology
City
Hershey
State/Province
Pennsylvania
ZIP/Postal Code
17033-0850
Country
United States
Facility Name
DermResearch, Inc.
City
Austin
State/Province
Texas
ZIP/Postal Code
78759
Country
United States
Facility Name
J & S Studies, Inc.
City
Bryan
State/Province
Texas
ZIP/Postal Code
77802
Country
United States
Facility Name
Stephens & Associates
City
Carrollton
State/Province
Texas
ZIP/Postal Code
75006
Country
United States
Facility Name
Dermatology Research Center
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84124
Country
United States
Facility Name
Virginia Clinical Research, Inc.
City
Norfolk
State/Province
Virginia
ZIP/Postal Code
23507
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Differin® Gel x12 Wks vs Tazorac® Cream x12 Wks vs Differin® x6 Wks Switched to Tazorac® x6 Wks for Treatment of Acne
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