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Safety and efficacy of adapalene 0.1% / benzoyl peroxide 2.5% in the long-term treatment of predominantly moderate acne with or without concomitant medication - results from the non-interventional cohort study ELANG.

Authors :
Gollnick, H.P.M.
Friedrich, M.
Peschen, M.
Pettker, R.
Pier, A.
Streit, V.
Jöstingmeyer, P.
Porombka, D.
Rojo Pulido, I.
Jäckel, A.
Source :
Journal of the European Academy of Dermatology & Venereology; Jun2015 Supplement, Vol. 29, p15-22, 8p
Publication Year :
2015

Abstract

Background Acne is a chronic inflammatory disease requiring long-term treatment. The fixed-dose combination adapalene 0.1%/benzoyl peroxide 2.5% (adapalene- BPO) is indicated for the once-daily topical treatment of Acne vulgaris when comedones, papules and pustules are present. Objective The main objectives of this non-interventional study were to assess long-term efficacy and safety of adapalene- BPO in moderate to severe acne with and without concomitant medication. Methods Patients with moderate to severe acne received adapalene- BPO alone or in combination with concomitant medication over a course of 9 months. The primary efficacy endpoint was changes in acne severity according to the Leeds Revised Acne Grading System; secondary endpoints included treatment success assessed by the patient and safety. Results In total, 5131 patients were eligible for efficacy and 5141 for safety evaluation. The majority of patients (78.8%) received adapalene- BPO alone. About 21.2% received adapalene- BPO in combination with another agent, mostly topical antibiotics (8.8%) or systemic antibiotics (8.7%). Mean (±SD) acne severity improved from 5.6 ± 1.5 at baseline to 3.3 ± 1.9 at month 3, and further to 1.9 ± 1.9 at month 9 (both P < 0.0001). The degree of improvement correlated significantly with the severity at baseline. After 3 and 9 months of treatment, the facial skin was cleared completely (no more visible acne lesions) in 420 (8.2%) and 1326 patients (25.8%), respectively. A therapeutic effect was noted by the patients after a median time of 3 weeks (range: from 1 day to 12 weeks). No serious adverse events were reported. Facial skin irritations, mostly mild to moderate, occurred in 49.5% of patients and led to discontinuation in only 1.7% of cases. Conclusion In consistence with previous clinical findings, the use of adapalene- BPO in daily practice routine is safe and effective in the long-term management of patients with moderate to severe acne. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09269959
Volume :
29
Database :
Complementary Index
Journal :
Journal of the European Academy of Dermatology & Venereology
Publication Type :
Academic Journal
Accession number :
103143352
Full Text :
https://doi.org/10.1111/jdv.13194