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临床试验/EUCTR2015-000561-31-BG
EUCTR2015-000561-31-BG进行中(未招募)1 期

A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PARALLEL, VEHICLE-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF P-3058 10% NAIL SOLUTION IN THE TREATMENT OF ONYCHOMYCOSIS

Polichem S.A.0 个研究点目标入组 980 人开始时间: 2015年7月7日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
980

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • - Written informed consent before starting any study related procedures.
  • - Adult patients aged 18 years and older of any race.
  • - Males or females.
  • - Patients with onychomycosis involving = 20% to = 50% of the area of the target big toenail.
  • - Patients with a positive KOH examination in the screening target big toenail sample.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 590
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 390

排除标准

  • - Woman who is pregnant, nursing an infant, or planning a pregnancy during the study period.
  • - Presence of yellow spikes” (defined as longitudinal streak extending from the free edge of the nail to the proximal edge) on the target nail.
  • - Presence of dermatophytoma (defined as thick masses of fungal hyphae and necrotic keratin between the nail plate and nail bed) on the target nail.
  • - Presence of nail thickness exceeding 2 mm.
  • - Patients with proximal subungual involvement (marker of immunosuppressed patient).
  • - Patients with severe plantar or moccasin tinea pedis (defined by blistering, pustules or inability to ambulate).
  • - Patients with nail abnormalities due to conditions like psoriasis, lichen planus, immune dysfunction, collagen-vascular diseases, peripheral vascular disease.
  • - Patients with life expectancy less than 2 years.
  • - Chemotherapy, immunosuppressive therapy in the 12 weeks prior to Screening visit (V1).
  • - Systemic corticosteroids, antimetabolites and immune-stimulants therapy in the 4 weeks prior to Screening visit (V1).
  • - HIV infection or any other immunodeficiency.
  • - Alcohol or substance abuse.
  • - Patients with history of allergic reactions to terbinafine or its excipients.

研究者

发起方
Polichem S.A.

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