An open study to evaluate the efficacy and safety of tazarotene gel (0.1%) in acne vulgaris

BACKGROUND: Tazarotene is a new third generation topical acetylenic retinoid. The present study was conducted to evaluate the efficacy and safety of tazarotene gel (0.1%) in Indian patients of acne vulgaris. METHODS: The present study was a prospective, open, multicentric, phase III trial. The durat...

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Published inIndian journal of dermatology, venereology, and leprology Vol. 70; no. 2; pp. 92 - 95
Main Author Saple DG, Torsekar RG, Pawanarkar Vikas , Dhanalakshmi UR, Ravichandran G, Kaur Daljeet , Dongre Neelesh , Desai Anish
Format Journal Article
LanguageEnglish
Published India Medknow Publications on behalf of The Indian Association of Dermatologists, Venereologists and Leprologists (IADVL) 01.03.2004
Medknow Publications and Media Pvt. Ltd
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Summary:BACKGROUND: Tazarotene is a new third generation topical acetylenic retinoid. The present study was conducted to evaluate the efficacy and safety of tazarotene gel (0.1%) in Indian patients of acne vulgaris. METHODS: The present study was a prospective, open, multicentric, phase III trial. The duration of study was 14 weeks, including a 12-week active treatment period, preceded by a 2-week washout phase. Patients applied 0.1% tazarotene gel as a thin film over the affected area once daily in the evening. The efficacy was evaluated by analyzing changes in the number of facial acne lesions and patient's and physicians' global assessment. The efficacy parameters were assessed at baseline, visits 2, 4, 8, and 12 weeks. Tolerability and safety was assessed by physical examination, laboratory parameters and evaluation of adverse events. RESULTS: A total of 126 patients in 6 centers completed the study. At the end of the 8th and 12th weeks, the mean number of inflammatory lesions reduced by 70.6% and 86.1%, non-inflammatory lesions by 81.5% and 92%, and total lesion count 75.6% and 88.8% respectively from baseline. Also, 90.7% and 93.6% of total study cases showed complete to moderate clearance of acne lesions according to physicians at the end of the 8th and 12th weeks. CONCLUSIONS: This study confirms the efficacy and safety of tazarotene gel (0.1%) in Indian patients of acne vulgaris.
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ISSN:0378-6323
0973-3922
1998-3611