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Comparative Efficacy and Safety of Benzoyl Peroxide Used in Combination With Clindamycin vs. Benzoyl Peroxide Used in Combination With Clindamycin and Doxycycline in the Treatment of Moderate Acne

Primary Purpose

Acne

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Benzoyl peroxide with clindamycin
Benzoyl peroxide with clindamycin and doxycycline
Sponsored by
Stiefel, a GSK Company
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acne focused on measuring Acne

Eligibility Criteria

16 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Male or female subjects with acne vulgaris . Able to understand the requirements of the study and sign informed consent/HIPAA authorization forms.

Exclusion Criteria:

  • Known hypersensitivity to any of the components of the study drugs or used of prohibited medications or any medical condition that contraindicate the subject's participation in the clinical study

Sites / Locations

  • Center for Dermatology, Cosmetic and Laser Surgery
  • Las Vegas Skin & Cancer Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

BPO with clindamycin foam

BPO + clindamycin foam + doxycycline

Arm Description

Benzoyl peroxide (BPO) wash with clindamycin foam

Benzoyl peroxide (BPO) wash with clindamycin foam and doxycycline capsules

Outcomes

Primary Outcome Measures

Percent Change in Inflammatory Acne Lesions From Baseline to Week 16
Percent change from baseline to week 16 in inflammatory acne lesions (pustules/papules)(chest and back)
Percent (%) Change in Non-inflammatory Acne Lesions From Baseline to Week 16.
Percent change in Non-inflammatory acne lesions (whiteheads and blackheads)(chest and back) from baseline to week 16.
Percent Change in Total Acne Lesion Counts From Baseline to Week 16
Percent change from baseline to week 16 in total acne lesions (inflammatory + non-inflammatory)
Change in Investigator Global Assessment (IGA)
Change in Investigator Global Assessment (IGA) Average values chest and back. IGA scale: 0 - Clear 0.5 - Clear/almost clear Almost Clear 1.5- Almost Clear/Mild Mild 2.5- Mild/Moderate Moderate 3.5- Moderate/Severe

Secondary Outcome Measures

Percent (%) Change in Inflammatory Lesion Counts (Chest and Back) From Baseline to Week 12
Percent change in inflammatory lesion counts (chest and back)from Baseline to Week 12
Percent Change in Non-inflammatory Lesions (Chest and Back) From Baseline to Week 12
Percent change in non-inflammatory lesions (chest and back) from baseline to Week 12
Percent Change in Total Lesions (Chest and Back) From Baseline to Week 12
Percent change in total lesions (chest and back) from baseline to Week 12
Percentage of Particpants With IGA Score at Week 16
Investigator Global Assessment (IGA) at Week 16 based on the Investigator Global Assessment IGA: 0 - Clear 0.5 - Clear/almost clear Almost Clear 1.5- Almost Clear/Mild Mild 2.5- Mild/Moderate Moderate 3.5- Moderate/Severe

Full Information

First Posted
February 4, 2009
Last Updated
May 24, 2017
Sponsor
Stiefel, a GSK Company
Collaborators
GlaxoSmithKline
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1. Study Identification

Unique Protocol Identification Number
NCT00837213
Brief Title
Comparative Efficacy and Safety of Benzoyl Peroxide Used in Combination With Clindamycin vs. Benzoyl Peroxide Used in Combination With Clindamycin and Doxycycline in the Treatment of Moderate Acne
Official Title
Comparative Efficacy and Safety of Benzoyl Peroxide Used in Combination With Clindamycin vs. Benzoyl Peroxide Used in Combination With Clindamycin and Doxycycline in the Treatment of Moderate Acne
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Completed
Study Start Date
August 2007 (undefined)
Primary Completion Date
August 2008 (Actual)
Study Completion Date
August 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Stiefel, a GSK Company
Collaborators
GlaxoSmithKline

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
To compare the efficacy and safety of Benzoyl peroxide used in combination with clindamycin vs. Benzoyl peroxide used in combination with clindamycin and doxycycline in the treatment of moderate acne
Detailed Description
To compare the efficacy and safety of Benzoyl peroxide used in combination with clindamycin vs. Benzoyl peroxide used in combination with clindamycin and doxycycline once daily in the treatment of moderate acne

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acne
Keywords
Acne

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
33 (Actual)

8. Arms, Groups, and Interventions

Arm Title
BPO with clindamycin foam
Arm Type
Active Comparator
Arm Description
Benzoyl peroxide (BPO) wash with clindamycin foam
Arm Title
BPO + clindamycin foam + doxycycline
Arm Type
Active Comparator
Arm Description
Benzoyl peroxide (BPO) wash with clindamycin foam and doxycycline capsules
Intervention Type
Drug
Intervention Name(s)
Benzoyl peroxide with clindamycin
Other Intervention Name(s)
Acne
Intervention Description
Benzoyl peroxide wash - Clindamycin foam
Intervention Type
Drug
Intervention Name(s)
Benzoyl peroxide with clindamycin and doxycycline
Other Intervention Name(s)
Acne
Intervention Description
Benzoyl peroxide wash - Clindamycin foam - Doxycycline capsules
Primary Outcome Measure Information:
Title
Percent Change in Inflammatory Acne Lesions From Baseline to Week 16
Description
Percent change from baseline to week 16 in inflammatory acne lesions (pustules/papules)(chest and back)
Time Frame
Baseline, Week 16
Title
Percent (%) Change in Non-inflammatory Acne Lesions From Baseline to Week 16.
Description
Percent change in Non-inflammatory acne lesions (whiteheads and blackheads)(chest and back) from baseline to week 16.
Time Frame
Baseline, Week 16
Title
Percent Change in Total Acne Lesion Counts From Baseline to Week 16
Description
Percent change from baseline to week 16 in total acne lesions (inflammatory + non-inflammatory)
Time Frame
Baseline, Week 16
Title
Change in Investigator Global Assessment (IGA)
Description
Change in Investigator Global Assessment (IGA) Average values chest and back. IGA scale: 0 - Clear 0.5 - Clear/almost clear Almost Clear 1.5- Almost Clear/Mild Mild 2.5- Mild/Moderate Moderate 3.5- Moderate/Severe
Time Frame
Baseline, Weeks 4, 8,12, and 16
Secondary Outcome Measure Information:
Title
Percent (%) Change in Inflammatory Lesion Counts (Chest and Back) From Baseline to Week 12
Description
Percent change in inflammatory lesion counts (chest and back)from Baseline to Week 12
Time Frame
Baseline, Week 12
Title
Percent Change in Non-inflammatory Lesions (Chest and Back) From Baseline to Week 12
Description
Percent change in non-inflammatory lesions (chest and back) from baseline to Week 12
Time Frame
Baseline, Week 12
Title
Percent Change in Total Lesions (Chest and Back) From Baseline to Week 12
Description
Percent change in total lesions (chest and back) from baseline to Week 12
Time Frame
Week 12
Title
Percentage of Particpants With IGA Score at Week 16
Description
Investigator Global Assessment (IGA) at Week 16 based on the Investigator Global Assessment IGA: 0 - Clear 0.5 - Clear/almost clear Almost Clear 1.5- Almost Clear/Mild Mild 2.5- Mild/Moderate Moderate 3.5- Moderate/Severe
Time Frame
Baseline, Week 16

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female subjects with acne vulgaris . Able to understand the requirements of the study and sign informed consent/HIPAA authorization forms. Exclusion Criteria: Known hypersensitivity to any of the components of the study drugs or used of prohibited medications or any medical condition that contraindicate the subject's participation in the clinical study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
GSK Clinical Trials
Organizational Affiliation
GlaxoSmithKline
Official's Role
Study Director
Facility Information:
Facility Name
Center for Dermatology, Cosmetic and Laser Surgery
City
Fremont
State/Province
California
ZIP/Postal Code
94538
Country
United States
Facility Name
Las Vegas Skin & Cancer Clinic
City
Las Vegas
State/Province
Nevada
ZIP/Postal Code
89129
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Comparative Efficacy and Safety of Benzoyl Peroxide Used in Combination With Clindamycin vs. Benzoyl Peroxide Used in Combination With Clindamycin and Doxycycline in the Treatment of Moderate Acne

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