A Study Comparing Clindamycin 1%/Benzoyl Peroxide 5% Topical Gel to Duac® Topical Gel in the Treatment of Acne Vulgaris
Overview[ - collapse ][ - ]
| Purpose | The objective of this study is to compare the relative efficacy and safety of the test formulation Clindamycin 1%/Benzoyl Peroxide 5% Topical Gel (Taro Pharmaceuticals Inc.) to the marketed formulation Duac® Topical Gel (Clindamycin 1%/Benzoyl Peroxide 5%) (Stiefel) in the treatment of the inflamed lesions of acne vulgaris. Both the test and reference formulations will also be compared to a placebo formulation to test for superiority. |
|---|---|
| Condition | Acne Vulgaris |
| Intervention | Drug: Clindamycin 1%/Benzoyl Peroxide 5% Topical Gel Drug: Duac® Topical Gel Drug: Placebo Topical Gel |
| Phase | Phase 1 |
| Sponsor | Taro Pharmaceuticals USA |
| Responsible Party | Taro Pharmaceuticals USA |
| ClinicalTrials.gov Identifier | NCT01769664 |
| First Received | October 11, 2012 |
| Last Updated | January 19, 2014 |
| Last verified | January 2014 |
Tracking Information[ + expand ][ + ]
| First Received Date | October 11, 2012 |
|---|---|
| Last Updated Date | January 19, 2014 |
| Start Date | September 2012 |
| Estimated Primary Completion Date | August 2013 |
| Current Primary Outcome Measures | Bioequivalence of test gel to reference gel [Time Frame: Week 11 (study day 77)] [Designated as safety issue: No]Bioequivalence will be determined by evaluating the mean percent change from baseline to week 11 in the number of inflammatory lesions. |
| Current Secondary Outcome Measures | Superiority against placebo [Time Frame: Week 11 (study day 77)] [Designated as safety issue: No]The superiority of the test and reference against the placebo will be tested for the mean percent reduction in inflamed lesion count at week 11. |
Descriptive Information[ + expand ][ + ]
| Brief Title | A Study Comparing Clindamycin 1%/Benzoyl Peroxide 5% Topical Gel to Duac® Topical Gel in the Treatment of Acne Vulgaris |
|---|---|
| Official Title | A Randomized, Double-Blind, Multiple-Site, Placebo-Controlled, Parallel Design Study Comparing Clindamycin 1%/Benzoyl Peroxide 5% Topical Gel (Taro Pharmaceuticals Inc.) to Duac® Topical Gel Clindamycin 1%/Benzoyl Peroxide 5% (Stiefel) in the Treatment of Acne Vulgaris |
| Brief Summary | The objective of this study is to compare the relative efficacy and safety of the test formulation Clindamycin 1%/Benzoyl Peroxide 5% Topical Gel (Taro Pharmaceuticals Inc.) to the marketed formulation Duac® Topical Gel (Clindamycin 1%/Benzoyl Peroxide 5%) (Stiefel) in the treatment of the inflamed lesions of acne vulgaris. Both the test and reference formulations will also be compared to a placebo formulation to test for superiority. |
| Detailed Description | Not Provided |
| Study Type | Interventional |
| Study Phase | Phase 1 |
| Study Design | Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment |
| Condition | Acne Vulgaris |
| Intervention | Drug: Clindamycin 1%/Benzoyl Peroxide 5% Topical Gel Clindamycin 1%/Benzoyl Peroxide 5% Topical Gel (Taro Pharmaceuticals Inc.) applied once a day in the evening for 77 days (11 weeks) Drug: Duac® Topical Gel Duac® (Clindamycin 1%/Benzoyl Peroxide 5%) Topical Gel (Stiefel) applied once a day in the evening for 77 days (11 weeks) Drug: Placebo Topical Gel Placebo (Vehicle) Topical Gel (Taro Pharmaceuticals Inc.) applied once a day in the evening for 77 days (11 weeks) |
| Study Arm (s) |
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Recruitment Information[ + expand ][ + ]
| Recruitment Status | Completed |
|---|---|
| Estimated Enrollment | 650 |
| Estimated Completion Date | August 2013 |
| Estimated Primary Completion Date | June 2013 |
| Eligibility Criteria | Inclusion Criteria: - Male or non-pregnant, non-lactating female, between 12 and 40 years of age with a clinical diagnosis of acne vulgaris. - Signed informed consent form. For a minor, the parent or legal guardian will sign the consent form and patient will sign assent to participate form. - If female of child-bearing potential, prepare to abstain from sexual intercourse or use a reliable method of contraception during the study. Patients on hormonal contraceptives must have been on the same for three months prior to baseline visit and continue throughout the duration of the study. - Have facial acne with 20 or more facial inflammatory lesions and 25 or more non-inflammatory lesions and 2 or less nodulocystic lesions and have an Investigator Global Assessment score of 2, 3 or 4. - Willing to comply with the study requirements and restrictions including refraining from the use of all other topical acne medications or antibiotics during the treatment period. Exclusion Criteria: - Patient has more than 2 facial nodular lesions. - Patient has active cystic acne. - Patient has acne conglobata. - Patients with excessive facial hair that would interfere with the diagnosis or assessment of acne. - Patients with tatoos or excessive facial scarring that may interfere with the evaluation of the patient's acne. - Patients with active facial sunburn, peeling due to sunburn and patients who will be exposed to excessive sunlight during the study. - Any skin condition other than acne vulgaris that would interfere with the evaluation of the patient's acne. - Females who are pregnant, lactating or likely to become pregnant during the study. - Patients with a history of or active colitis other than irritable bowel syndrome. - History of allergy or hypersensitivity to Clindamycin, Lincomycin or benzoyl peroxide or history of any drug hypersensitivity or intolerance which would compromise the patient's safety or the study. - Significant history or current evidence of chronic infectious disease, system disorder, organ disorder or other medical condition that would place the patient at undue risk by participation. - Use on the face within 1 month prior to screening/baseline or during the study of the following: cryodestruction or chemodestruction, dermabrasion, photodynamic therapy, acne surgery, intralesional steroids, x-ray therapy. - Use of the following within 1 month prior to screening/baseline: spironolactone, systemic steroids, systemic antibiotics, systemic treatment for acne vulgaris (other than oral retinoids which require a 6 month washout), systemic anti-inflammatory agents. - Use of oral isotretinoin (Accutane®) or oral retinoids within 6 months, or therapeutic vitamin A supplements greater than 10,000 units/day. - Use within 2 weeks prior to screening/baseline of the following: topical steroids, topical retinoids, topical acne treatments including over-the-counter preparations, topical anti-inflammatory agents, medicated cleansers, topical antibiotics. - Receipt of any drug as part of a research study within 30 days. - Female patients taking hormonal contraceptives or oral estrogen for less than 3 months and those that plan to change the dosage regimen during the course of the study. - Previous participation in this study. - Employees of the investigator or research center or their immediate family members. |
| Gender | Both |
| Ages | 12 Years |
| Accepts Healthy Volunteers | No |
| Contacts | Not Provided |
| Location Countries | Not Provided |
Administrative Information[ + expand ][ + ]
| NCT Number | NCT01769664 |
|---|---|
| Other Study ID Numbers | CLBG 1209 |
| Has Data Monitoring Committee | No |
| Information Provided By | Taro Pharmaceuticals USA |
| Study Sponsor | Taro Pharmaceuticals USA |
| Collaborators | Not Provided |
| Investigators | Not Provided |
| Verification Date | January 2014 |