These clinical study results are supplied for informational purposes only in the interests of scientific disclosure. They are not intended to substitute for the FDA-approved package insert or other approved labeling. Drug Details Company Name Business Partner Drug Name Generic Name Unique ID Studied Indications or Disease Phase Approved Drug Label sanofi-aventis BENZACLIN TOPICAL/DUAC TOPICAL CLINDAMYCIN 1% / BENZOYL PEROXIDE 5% NCT00377000 Acne Phase IV US: http://products.sanofi-aventis.us/benzaclin/benzaclin.html Other: Refer to local approved drug label. Clinical Study Summary DL6021-0505 This study was performed in the United States (US) An american pilot, multicenter patient preference study comparing two clindamycin/benzoyl peroxide gels. The summary result information on clinical trials is provided by the sanofi-aventis Group for informational purposes only and is not intended to promote any product or use. Summaries of clinical study results are intended to report the results of the study that were known at the time of the study’s completion. The summaries therefore do not provide a comprehensive and current review of the safety and efficacy of any drug based upon all information available, and the sanofi-aventis Group makes no representation or warranty of any kind as to the currency or completeness of the information contained in any summary, and disclaims all warranties, express or implied, with respect to such information. Healthcare Professionals should refer to the current approved product labeling for information on approved indications in their country. This information is not intended to replace the advice of a health care professional. Only a physician can determine if a specific medicine is the correct or best treatment option for a particular patient. If you have questions, please consult a health care professional. Company Study Clinical Study Report Synopsis Back to Search Results