Reformulations of well‐known active ingredients in the topical treatment of psoriasis vulgaris can improve clinical outcomes for patients

Although the majority of patients with psoriasis vulgaris are treated exclusively with topical therapies, research to develop more effective topical therapies that are associated with higher patient satisfaction has lagged behind the development of systemic agents. The aim of this literature review...

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Veröffentlicht in:Journal of the European Academy of Dermatology and Venereology 2017-08, Vol.31 (8), p.1271-1284
Hauptverfasser: Iversen, L., Dauden, E., Segaert, S., Freeman, K., Magina, S., Rigopoulos, D., Thaci, D.
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container_end_page 1284
container_issue 8
container_start_page 1271
container_title Journal of the European Academy of Dermatology and Venereology
container_volume 31
creator Iversen, L.
Dauden, E.
Segaert, S.
Freeman, K.
Magina, S.
Rigopoulos, D.
Thaci, D.
description Although the majority of patients with psoriasis vulgaris are treated exclusively with topical therapies, research to develop more effective topical therapies that are associated with higher patient satisfaction has lagged behind the development of systemic agents. The aim of this literature review was to determine whether there is documented evidence that applying an innovative approach to improving the formulation of active ingredients commonly used in the topical treatment of psoriasis can have a positive effect on clinical outcomes and patient‐reported outcomes (PROs). The Embase and PubMed databases were searched for articles published between 2001 and 2016 that made direct head‐to‐head comparisons of different formulations of an active pharmaceutical ingredient (API), focusing on clinical outcomes and PROs. In total, 22 publications on APIs or API combinations met the eligibility criteria (19 head‐to‐head clinical trials, one pooled analysis, one health‐economic modelling study and one systematic review). Significant clinical benefit associated with the use of a reformulated API over an older formulation was reported in three trials of clobetasol propionate, one trial of calcipotriol, three trials of betamethasone and five trials/pooled analyses of calcipotriol/calcipotriene + betamethasone dipropionate (Cal/BD) formulations. Significantly improved PROs associated with the use of a reformulated API over an older formulation were reported in three trials of clobetasol propionate, one trial of betamethasone valerate and two trials of Cal/BD formulations. These results demonstrate that the innovative reformulation of APIs used in the treatment of psoriasis can produce therapies that attain significantly improved clinical outcomes and PROs. This suggests that improvement in topical therapy for psoriasis need not only to be achieved by the identification of new targets and the development of new APIs, but that improvement in the vehicle used to deliver existing APIs has the potential to result in significant clinical and patient benefits.
doi_str_mv 10.1111/jdv.14277
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subjects Administration, Topical
Dermatologic Agents - administration & dosage
Dermatologic Agents - therapeutic use
Drug Compounding
Humans
Psoriasis - drug therapy
Treatment Outcome
title Reformulations of well‐known active ingredients in the topical treatment of psoriasis vulgaris can improve clinical outcomes for patients
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