Efficacy of Topical Azelaic Acid 15% Gel Plus Anti-inflammatory Dose Doxycycline or Metronidazole Gel 1% Plus Anti-inflammatory Dose Doxycycline in Moderate Papulopustular Rosacea
Primary Purpose
Papulopustular Rosacea
Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Azelaic acid (Finacea, BAY39-6251)
Metronidazole (Metrogel)
Doxycycline (Oracea)
Sponsored by
About this trial
This is an interventional treatment trial for Papulopustular Rosacea focused on measuring Rosacea
Eligibility Criteria
Inclusion Criteria:
- Moderate papulopustular rosacea (IGA>4) with a minimum of 10 and no more than 50 inflammatory lesions and persistent erythema with or without telangiectasia
Exclusion Criteria:
- Sensitivity to any of the treatments used
- Co-existing conditions that would unfavorably influence the course of the disease
- Pregnant or lactating women
- Severe rosacea
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Azelaic acid (Finacea, BAY39-6251) plus Doxycycline (Oracea)
Metronidazole (Metrogel) plus Doxycycline (Oracea)
Arm Description
Participants received topical azelaic acid gel 15% twice daily and doxycycline 40 mg once daily for 12 weeks
Participants received topical metronidazole 1% gel once daily and doxycycline 40 mg once daily for 12 weeks
Outcomes
Primary Outcome Measures
Nominal Change From Baseline in Inflammatory Lesion (IL) Count (Sum of Papules and Pustules) at Week 2 (LOCF: Last Observation Carried Forward)
NOTE: Negative mean values represent an improvement (decrease of inflammatory lesions)
Secondary Outcome Measures
Number of Inflammatory Lesions at Weeks 2, 4, 6, 8 and 12 (LOCF)
Nominal Change From Baseline in IL Count at Weeks 4, 6, 8 and 12 (LOCF)
NOTE: Negative mean values represent an improvement (decrease of inflammatory lesions)
Percent Change From Baseline in IL Count at Weeks 2, 4, 6, 8 and 12 (LOCF)
NOTE: Negative mean values represent an improvement (decrease of inflammatory lesions)
Percentage of Participants With at Least a 25%, 50%, or 75% Improvement in Facial IL Counts From Baseline to Weeks 2, 4, 6, 8 and 12 (LOCF)
Percentage of Participants With Investigator's Global Assessment (IGA) Based Therapeutic Success at Weeks 2, 4, 6, 8 and 12 (LOCF)
IGA categories: 0 - Clear; 1 - Minimal; 2 - Mild; 3 - Mild to moderate; 4 - Moderate; 5 - Moderate to severe; 6 - Severe (refer to Detailed Description field in Protocol section for more information) / Therapeutic success is defined as an IGA score of clear or minimal (0 or 1).
Percentage of Participants With IGA Based Patient Response at Weeks 2, 4, 6, 8 and 12 (LOCF)
IGA categories: 0 - Clear; 1 - Minimal; 2 - Mild; 3 - Mild to moderate; 4 - Moderate; 5 - Moderate to severe; 6 - Severe (refer to Detailed Description field in Protocol section for more information) / Patient response is defined as an IGA score of clear, minimal, or mild (0, 1, or 2)
Percentage of Participants With Respective Disease Severity Measured by IGA Scores at Week 2
IGA categories: 0 - Clear; 1 - Minimal; 2 - Mild; 3 - Mild to moderate; 4 - Moderate; 5 - Moderate to severe; 6 - Severe (refer to Detailed Description field in Protocol section for more information).
Percentage of Participants With Respective Disease Severity Measured by IGA Scores at Week 4
IGA categories: 0 - Clear; 1 - Minimal; 2 - Mild; 3 - Mild to moderate; 4 - Moderate; 5 - Moderate to severe; 6 - Severe (refer to Detailed Description field in Protocol section for more information).
Percentage of Participants With Respective Disease Severity Measured by IGA Scores at Week 6
IGA categories: 0 - Clear; 1 - Minimal; 2 - Mild; 3 - Mild to moderate; 4 - Moderate; 5 - Moderate to severe; 6 - Severe (refer to Detailed Description field in Protocol section for more information).
Percentage of Participants With Respective Disease Severity Measured by IGA Scores at Week 8
IGA categories: 0 - Clear; 1 - Minimal; 2 - Mild; 3 - Mild to moderate; 4 - Moderate; 5 - Moderate to severe; 6 - Severe (refer to Detailed Description field in Protocol section for more information).
Percentage of Participants With Respective Disease Severity Measured by IGA Scores at Week 12
IGA categories: 0 - Clear; 1 - Minimal; 2 - Mild; 3 - Mild to moderate; 4 - Moderate; 5 - Moderate to severe; 6 - Severe (refer to Detailed Description field in Protocol section for more information).
Investigator Rating of Overall Improvement at End of Study (Week 12)
Patient Rating of Overall Improvement at End of Study (Week 12)
Patient Opinion of Cosmetic Acceptability at End of Study (Week 12)
Full Information
NCT ID
NCT00855595
First Posted
March 3, 2009
Last Updated
March 30, 2020
Sponsor
LEO Pharma
Collaborators
Bayer
1. Study Identification
Unique Protocol Identification Number
NCT00855595
Brief Title
Efficacy of Topical Azelaic Acid 15% Gel Plus Anti-inflammatory Dose Doxycycline or Metronidazole Gel 1% Plus Anti-inflammatory Dose Doxycycline in Moderate Papulopustular Rosacea
Official Title
An Exploratory, Multicenter, Investigator-blinded, Active-controlled Study to Investigate the Efficacy of Topical Azelaic Acid (AzA)15% Gel Twice Daily or Metronidazole Topical Gel 1% Once Daily, Plus Anti-inflammatory Dose Doxycycline (40mg) Once Daily in Subjects With Moderate Papulopustular Rosacea
Study Type
Interventional
2. Study Status
Record Verification Date
January 2014
Overall Recruitment Status
Completed
Study Start Date
February 2009 (undefined)
Primary Completion Date
April 2009 (Actual)
Study Completion Date
July 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
LEO Pharma
Collaborators
Bayer
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Subjects with moderate papulopustular rosacea will be treated either with azelaic acid 15% gel topically plus an anti-inflammatory dose of doxycyline (40mg) daily or with metronidazole 1% gel topically once daily plus an anti-inflammatory dose of doxycycline (40mg) over at total of twelve weeks to determine the rapidity of improvement, and the length of time to reach 25%, 50% and 75% clearing compared to baseline.
Detailed Description
The change in inflammatory lesion count will be assessed at each post-baseline visit by an analysis of variance model (ANOVA) with factors treatment and center, but not including treatment-by-center interaction.
Investigator's Global Assessment (IGA) of papulopustular rosacea (static score): 0 - Clear (Virtually no rosacea ie, no papules and/or pustules; no or residual erythema; no or mild to moderate degree of telangiectasia may be present); 1 - Minimal (Rare papules and/or pustules; residual to mild erythema; mild to moderate degree of telangiectasia may be present); 2 - Mild (Few papules and/or pustules; mild erythema; mild to moderate degree of telangiectasia may be present); 3 - Mild to moderate (Distinct number of papules and/or pustules; mild to moderate erythema; mild to moderate degree of telangiectasia may be present); 4 - Moderate (Pronounced number of papules and/or pustules; moderate erythema; mild to moderate degree of telangiectasia may be present); 5 - Moderate to severe (Many papules and/or pustules, occasionally with large inflamed lesions; moderate erythema; moderate degree of telangiectasia may be present); 6 - Severe (Numerous papules and/or pustules, occasionally with confluent areas of inflamed lesions; moderate or severe erythema; moderate or severe degree of telangiectasia may be present).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Papulopustular Rosacea
Keywords
Rosacea
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
207 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Azelaic acid (Finacea, BAY39-6251) plus Doxycycline (Oracea)
Arm Type
Experimental
Arm Description
Participants received topical azelaic acid gel 15% twice daily and doxycycline 40 mg once daily for 12 weeks
Arm Title
Metronidazole (Metrogel) plus Doxycycline (Oracea)
Arm Type
Active Comparator
Arm Description
Participants received topical metronidazole 1% gel once daily and doxycycline 40 mg once daily for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Azelaic acid (Finacea, BAY39-6251)
Intervention Description
Participants received topical azelaic acid gel 15% twice daily for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Metronidazole (Metrogel)
Intervention Description
Participants received topical metronidazole 1% gel once daily for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Doxycycline (Oracea)
Intervention Description
Participants received systemic doxycycline 40 mg once daily for 12 week
Primary Outcome Measure Information:
Title
Nominal Change From Baseline in Inflammatory Lesion (IL) Count (Sum of Papules and Pustules) at Week 2 (LOCF: Last Observation Carried Forward)
Description
NOTE: Negative mean values represent an improvement (decrease of inflammatory lesions)
Time Frame
Baseline and Week 2
Secondary Outcome Measure Information:
Title
Number of Inflammatory Lesions at Weeks 2, 4, 6, 8 and 12 (LOCF)
Time Frame
Week 2, 4, 6, 8 and 12
Title
Nominal Change From Baseline in IL Count at Weeks 4, 6, 8 and 12 (LOCF)
Description
NOTE: Negative mean values represent an improvement (decrease of inflammatory lesions)
Time Frame
Baseline and Week 4, 6, 8 and 12
Title
Percent Change From Baseline in IL Count at Weeks 2, 4, 6, 8 and 12 (LOCF)
Description
NOTE: Negative mean values represent an improvement (decrease of inflammatory lesions)
Time Frame
Baseline and Week 2, 4, 6, 8 and 12
Title
Percentage of Participants With at Least a 25%, 50%, or 75% Improvement in Facial IL Counts From Baseline to Weeks 2, 4, 6, 8 and 12 (LOCF)
Time Frame
Baseline and Weeks 2, 4, 6, 8 and 12
Title
Percentage of Participants With Investigator's Global Assessment (IGA) Based Therapeutic Success at Weeks 2, 4, 6, 8 and 12 (LOCF)
Description
IGA categories: 0 - Clear; 1 - Minimal; 2 - Mild; 3 - Mild to moderate; 4 - Moderate; 5 - Moderate to severe; 6 - Severe (refer to Detailed Description field in Protocol section for more information) / Therapeutic success is defined as an IGA score of clear or minimal (0 or 1).
Time Frame
Weeks 2, 4, 6, 8 and 12
Title
Percentage of Participants With IGA Based Patient Response at Weeks 2, 4, 6, 8 and 12 (LOCF)
Description
IGA categories: 0 - Clear; 1 - Minimal; 2 - Mild; 3 - Mild to moderate; 4 - Moderate; 5 - Moderate to severe; 6 - Severe (refer to Detailed Description field in Protocol section for more information) / Patient response is defined as an IGA score of clear, minimal, or mild (0, 1, or 2)
Time Frame
Weeks 2, 4, 6, 8 and 12
Title
Percentage of Participants With Respective Disease Severity Measured by IGA Scores at Week 2
Description
IGA categories: 0 - Clear; 1 - Minimal; 2 - Mild; 3 - Mild to moderate; 4 - Moderate; 5 - Moderate to severe; 6 - Severe (refer to Detailed Description field in Protocol section for more information).
Time Frame
At Week 2
Title
Percentage of Participants With Respective Disease Severity Measured by IGA Scores at Week 4
Description
IGA categories: 0 - Clear; 1 - Minimal; 2 - Mild; 3 - Mild to moderate; 4 - Moderate; 5 - Moderate to severe; 6 - Severe (refer to Detailed Description field in Protocol section for more information).
Time Frame
At Week 4
Title
Percentage of Participants With Respective Disease Severity Measured by IGA Scores at Week 6
Description
IGA categories: 0 - Clear; 1 - Minimal; 2 - Mild; 3 - Mild to moderate; 4 - Moderate; 5 - Moderate to severe; 6 - Severe (refer to Detailed Description field in Protocol section for more information).
Time Frame
At Week 6
Title
Percentage of Participants With Respective Disease Severity Measured by IGA Scores at Week 8
Description
IGA categories: 0 - Clear; 1 - Minimal; 2 - Mild; 3 - Mild to moderate; 4 - Moderate; 5 - Moderate to severe; 6 - Severe (refer to Detailed Description field in Protocol section for more information).
Time Frame
At Week 8
Title
Percentage of Participants With Respective Disease Severity Measured by IGA Scores at Week 12
Description
IGA categories: 0 - Clear; 1 - Minimal; 2 - Mild; 3 - Mild to moderate; 4 - Moderate; 5 - Moderate to severe; 6 - Severe (refer to Detailed Description field in Protocol section for more information).
Time Frame
At Week 12
Title
Investigator Rating of Overall Improvement at End of Study (Week 12)
Time Frame
Week 12
Title
Patient Rating of Overall Improvement at End of Study (Week 12)
Time Frame
Week 12
Title
Patient Opinion of Cosmetic Acceptability at End of Study (Week 12)
Time Frame
Week 12
Other Pre-specified Outcome Measures:
Title
Patient Opinion of Local Tolerability
Time Frame
Week 12
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
- Moderate papulopustular rosacea (IGA>4) with a minimum of 10 and no more than 50 inflammatory lesions and persistent erythema with or without telangiectasia
Exclusion Criteria:
Sensitivity to any of the treatments used
Co-existing conditions that would unfavorably influence the course of the disease
Pregnant or lactating women
Severe rosacea
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bayer Study Director
Organizational Affiliation
Bayer
Official's Role
Study Director
Facility Information:
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35233
Country
United States
City
Denver
State/Province
Colorado
ZIP/Postal Code
80209
Country
United States
City
West Palm Beach
State/Province
Florida
ZIP/Postal Code
33401
Country
United States
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114-2517
Country
United States
City
Warren
State/Province
Michigan
ZIP/Postal Code
48088
Country
United States
City
Fridley
State/Province
Minnesota
ZIP/Postal Code
55432
Country
United States
City
Henderson
State/Province
Nevada
ZIP/Postal Code
89052
Country
United States
City
Albuquerque
State/Province
New Mexico
ZIP/Postal Code
87106
Country
United States
City
Stony Brook
State/Province
New York
ZIP/Postal Code
11790
Country
United States
City
Mason
State/Province
Ohio
ZIP/Postal Code
45040
Country
United States
City
Portland
State/Province
Oregon
ZIP/Postal Code
97223
Country
United States
City
Austin
State/Province
Texas
ZIP/Postal Code
78759
Country
United States
City
Dallas
State/Province
Texas
ZIP/Postal Code
75246
Country
United States
City
Houston
State/Province
Texas
ZIP/Postal Code
77056
Country
United States
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78229
Country
United States
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84124
Country
United States
City
Norfolk
State/Province
Virginia
ZIP/Postal Code
23507
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
20645521
Citation
Del Rosso JQ, Bruce S, Jarratt M, Menter A, Staedtler G. Efficacy of topical azelaic acid (AzA) gel 15% plus oral doxycycline 40 mg versus metronidazole gel 1% plus oral doxycycline 40 mg in mild-to-moderate papulopustular rosacea. J Drugs Dermatol. 2010 Jun;9(6):607-13.
Results Reference
result
Learn more about this trial
Efficacy of Topical Azelaic Acid 15% Gel Plus Anti-inflammatory Dose Doxycycline or Metronidazole Gel 1% Plus Anti-inflammatory Dose Doxycycline in Moderate Papulopustular Rosacea
We'll reach out to this number within 24 hrs