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用于甲癣的研究性药物。

Investigational drugs for onychomycosis.

作者信息

Gupta Aditya K, Simpson Fiona C

机构信息

Department of Medicine, University of Toronto , Toronto, Ontario , Canada +1 519 657 4222 ext. 277 ; +1 519 657 4233 ;

出版信息

Expert Opin Investig Drugs. 2014 Jan;23(1):97-106. doi: 10.1517/13543784.2013.840289. Epub 2013 Sep 26.

Abstract

INTRODUCTION

Onychomycosis is the fungal infection of the nail plate by dermatophytes, yeasts and nondermatophyte molds. The treatment of onychomycosis poses many challenges due to low initial cure rates and a high rate of relapse and recurrence. Oral therapy is limited by adverse events and drug-drug interactions, whereas topical therapy has limited penetrance through the nail plate.

AREAS COVERED

New and reformulated drugs are in development for the treatment of onychomycosis. Experimental molecules include both oral and topical azole molecules, topical reformulations of terbinafine, the benzoxaboroles tavaborole and AN2718, the aganocide NVC-422 and the photosensitizer Sylsens B. These drugs are in varying stages of development so results from in vitro studies to Phase III clinical trials are discussed to present a complete picture of the current development pipeline for onychomycosis.

EXPERT OPINION

The development of new molecules from familiar and novel classes for both oral and topical administration is encouraging. It is clear that there is currently more emphasis on the development of topical drugs than orals, due to their lower potential for adverse events and drug-drug interactions. The emergence of novel molecular targets is encouraging for the possibility of combination therapy and any future drug-resistant strains of fungi.

摘要

引言

甲癣是由皮肤癣菌、酵母菌和非皮肤癣菌霉菌引起的甲板真菌感染。由于初始治愈率低、复发率和再发率高,甲癣的治疗面临诸多挑战。口服疗法受到不良事件和药物相互作用的限制,而局部疗法通过甲板的渗透率有限。

涵盖领域

正在研发用于治疗甲癣的新型和重新配方的药物。实验性分子包括口服和局部用唑类分子、特比萘芬的局部重新配方、苯并硼唑他伏硼罗和AN2718、杀线虫剂NVC - 422和光敏剂Sylsens B。这些药物处于不同的研发阶段,因此讨论了从体外研究到III期临床试验的结果,以全面呈现目前甲癣研发管线的情况。

专家意见

研发用于口服和局部给药的熟悉和新型类别的新分子令人鼓舞。显然,由于局部药物不良事件和药物相互作用的可能性较低,目前对局部药物研发的重视程度高于口服药物。新型分子靶点的出现对于联合治疗以及未来任何耐药真菌菌株的可能性而言是令人鼓舞的。

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