IJDVL Home  
 

STUDIES
[View FULLTEXT] [Download PDF]  
Year : 2004  |  Volume : 70  |  Issue : 2  |  Page : 92-95

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

DG Saple1, RG Torsekar2, Vikas Pawanarkar3, UR Dhanalakshmi4, G Ravichandran5, Daljeet Kaur6, Neelesh Dongre7, Anish Desai7 
1 Department of Dermatology, G. T. Hospital, Mumbai, India
2 Department of Dermatology, Rajiv Gandhi Medical College, Kalwa, Thane, India
3 Consultant Dermatologist, Pramila Hospital, Kalwa, Thane, India
4 Consultant Dermatologist, B. R. Hospital, Chennai, India
5 Department of Dermatology, Stanley Medical College and Hospital, Chennai, India
6 Consultant Dermatologist, Indus Hospital, Mohali, India
7 Glenmark Pharmaceuticals Ltd, Mumbai, India

Correspondence Address:
Neelesh Dongre
Manager - Medical Services, Glenmark Pharmaceuticals Ltd., 801-813, Mahalaxmi Chambers, 22, Bhulabhai Desai Road, Mumbai - 400026
India

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«SQ»s and physicians«SQ» 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.


How to cite this article:
Saple D G, Torsekar R G, Pawanarkar V, Dhanalakshmi U R, Ravichandran G, Kaur D, Dongre N, Desai A. An open study to evaluate the efficacy and safety of tazarotene gel (0.1%) in acne vulgaris.Indian J Dermatol Venereol Leprol 2004;70:92-95


How to cite this URL:
Saple D G, Torsekar R G, Pawanarkar V, Dhanalakshmi U R, Ravichandran G, Kaur D, Dongre N, Desai A. An open study to evaluate the efficacy and safety of tazarotene gel (0.1%) in acne vulgaris. Indian J Dermatol Venereol Leprol [serial online] 2004 [cited 2021 Jan 24 ];70:92-95
Available from: https://www.ijdvl.com/article.asp?issn=0378-6323;year=2004;volume=70;issue=2;spage=92;epage=95;aulast=Saple;type=0


 

Sunday, January 24, 2021
 Site Map | Home | Contact Us | Feedback | Copyright and disclaimer