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临床试验/JPRN-jRCT2080224871
JPRN-jRCT2080224871已完成3 期

A Phase III, Placebo-controlled, Randomized, Double-blind, Multicenter, Parallel-group comparative study to Evaluate the Efficacy and Safety of Patient Initiated Therapy of ASP2151 in Patients with Recurrent Genital Herpes

Maruho Co., Ltd.0 个研究点目标入组 578 人开始时间: 2019年9月13日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
578

研究概览

简要总结

In this study, amenamevir significantly shortened the time to all lesion healing of recurrent genital herpes over placebo. Amenamevir was well tolerated and showed no clinically major safety concerns.

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 18age old 至 <= 79age old(—)
性别
All

入选标准

  • •Recurrent Genital Herpes patients

排除标准

  • •(1)Patients diagnosed with immunodeficiency or immunocompromised function (such as patients with congenital immunodeficiency, AIDS patients, patients with HIV infection)
  • •(2)Patients with any disorders that should not be enrolled in the sutdy such as;
  • •-severe cardiac disorders
  • •-severe hepatic disorders
  • •-severe pulmonary disorders
  • •-severe blood disorders
  • •(3)Pregnant women, women who may be pregnant, lactating women or women who wish to become pregnant or women who are unwilling to use a suitable method of contraception as directed by the principal investigator or sub-investigator.

研究者

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