此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Study to Compare GS-1179 Versus Valacyclovir in HSV-2 Seropositive Participants With Recurrent Genital Herpes

2026年10月28日 更新者:Gilead Sciences

A Phase 2b, Randomized, Double-Blind, Active-Control, Parallel-Group Study to Evaluate the Safety and Efficacy of GS-1179 Versus Valacyclovir in HSV-2 Seropositive Participants With Recurrent Genital Herpes

The goal of this clinical study is to compare the study drug GS-1179, versus valacyclovir (VACV) in herpes simplex virus type 2 (HSV-2) seropositive participants with recurrent genital herpes.

The primary objective of this study are to evaluate the safety and tolerability of GS-1179 versus VACV and to evaluate the antiviral effect of GS-1179 versus VACV.

研究概览

研究类型

介入性

注册 (估计的)

300

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Key Inclusion Criteria:

  • Individuals assigned male or female at birth, 18 years of age or older at screening, able to understand and give written informed consent and comply with treatment and follow up. Individuals assigned male or female at birth who are of childbearing potential and engage in heterosexual intercourse must be nonpregnant, nonlactating, and agree to use protocol-specified method(s) of contraception.
  • Individual is HSV-2 seropositive (or HSV-1 seropositive AND HSV-2 seropositive)
  • Individual has a history of recurrent genital herpes for at least 1 year, with 4 to 9 clinical occurrences in the last year or, if currently on suppressive therapy, 4 to 9 occurrences a year prior to initiating suppressive therapy.
  • Other than HSV infection, individual is in good health (as determined by the investigator). Medical history and physical examination should be without clinically significant abnormalities.

Key Exclusion Criteria:

  • Individual has an acute episode of genital herpes during screening or on Day 1 prior to dosing.
  • Individual has any other clinically significant medical, behavioral, mental condition, substance use disorder, or pharmacologic or surgical treatment that, in the opinion of the investigator or the sponsor, may interfere with efficacy or safety assessments, or the absorption, distribution, and/or elimination of the study drug, or make the individual unsuitable for study participation.
  • Individual has a history of refractory or resistant HSV infection to any HSV-specific nucleoside analog including valacyclovir, acyclovir, famciclovir, penciclovir, ganciclovir, or valganciclovir.
  • Individual has had treatment with any investigational or approved helicase-primase inhibitor (HPI) (including ABI-5366, ABI-1179, pritelivir, adibelivir [IM-250], amenamavir) or received an investigational HSV vaccine. However, individuals may be eligible if they participated in an investigational HPI study or an investigational HSV vaccine study but have sponsor documentation that they did not receive active product (eg, placebo recipients).

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
实验性的:GS-1179 High Dose + VACV Placebo to Match (PTM)

Participants will be randomized to receive a high-dose of GS-1179 once weekly up to 85 days and VACV PTM once daily up to 92 days.

Administered orally

Administered orally

实验性的:GS-1179 Low Dose + VACV Placebo to Match (PTM)

Participants will be randomized to receive a low-dose of GS-1179 once weekly up to 85 days and VACV PTM once daily up to 92 days.

Administered orally

Administered orally

有源比较器:VACV + GS-1179 PTM

Participants will be randomized to receive VACV once daily up to 92 days and GS-1179 PTM once weekly up to 85 days.

Administered orally

Administered orally

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Percentage of Participants Experiencing Adverse Events (AEs)
大体时间:Enrollment up to 92 days
Enrollment up to 92 days
Percentage of Participants Experiencing Premature Study-Dug Discontinuation due to AEs
大体时间:Enrollment up to 92 days
Enrollment up to 92 days
Percentage of Participants Experiencing Treatment-Emergent Laboratory Abnormalities
大体时间:First dose date up to 92 days
First dose date up to 92 days
Herpes Simplex Virus Type 2 (HSV-2) Shedding Rate During the Swabbing Period
大体时间:Day 8 to Day 38
Day 8 to Day 38

次要结果测量

结果测量
措施说明
大体时间
Proportion of Participants Free of Genital Herpes Recurrences at Day 92
大体时间:Day 92
Day 92
Proportion of Participants Free of Genital Herpes Recurrences at Day 120
大体时间:Day 120
Day 120
Genital Herpes Lesion Rate During the Treatment Period
大体时间:Up to 92 days
Up to 92 days
Genital Herpes Lesion Duration During the Treatment Period
大体时间:Up to 92 days
Up to 92 days
Virologically Confirmed Genital Herpes Lesion Rate During the Treatment Period
大体时间:Up to 92 days
Up to 92 days
Virologically Confirmed Genital Herpes Lesion Duration During the Treatment Period
大体时间:Up to 92 days
Up to 92 days
Time to Suppression of HSV-2 Shedding
大体时间:Up to 92 days
Up to 92 days
Number of HSV-2 Shedding Episodes During the Swabbing Period
大体时间:Day 8 to Day 38
Day 8 to Day 38
Duration of HSV-2 Shedding Episodes During the Swabbing Period
大体时间:Day 8 to Day 38
Day 8 to Day 38
Proportion of Participants With Subclinical HSV-2 Shedding During the Swabbing Period
大体时间:Day 8 to Day 38

Subclinical HSV-2 shedding is defined as swabs testing positive for HSV-2 DNA during the Swabbing Period that are not accompanied by lesions.

Day 8 to Day 38
HSV-2 DNA (Copies/mL) for Swab Samples that are Positive for HSV-2 DNA During the Swabbing Period
大体时间:Day 8 to Day 38
Day 8 to Day 38
HSV-2 DNA (Copies/mL) for Positive Swab Samples in the Absence of Lesions (Subclinical Shedding) During the Swabbing Period
大体时间:Day 8 to Day 38
Day 8 to Day 38
Proportion of Swab Samples With HSV-2 DNA > 4 log10 Copies/mL for Positive Swab Samples During the Swabbing Period
大体时间:Day 8 to Day 38
Day 8 to Day 38
Proportion of Swab Samples With HSV-2 DNA > 4 log10 Copies/mL for Positive Swab Samples in the Absence of Lesions (Subclinical Shedding) During the Swabbing Period
大体时间:Day 8 to Day 38
Day 8 to Day 38
Plasma Pharmacokinetic (PK) Parameters: Cmax of GS-1179
大体时间:Day 1 up to 92 days

Cmax is defined as the maximum observed concentration of drug at steady state.

Day 1 up to 92 days
Plasma PK Parameters: AUCtau of GS-1179
大体时间:Day 1 up to 92 days

AUCtau is defined as the area under the concentration versus time curve over the dosing interval at steady state.

Day 1 up to 92 days
Plasma PK Parameters: Ctrough of GS-1179
大体时间:Day 1 up to 92 days

Ctrough is defined as the observed drug concentration at the end of the dosing interval at steady state.

Day 1 up to 92 days

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 研究主任:Gilead Study Director、Gilead Sciences

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年11月1日

初级完成 (估计的)

2027年11月1日

研究完成 (估计的)

2027年11月1日

研究注册日期

首次提交

2026年10月28日

首先提交符合 QC 标准的

2026年10月28日

首次发布 (实际的)

2026年11月3日

研究记录更新

最后更新发布 (实际的)

2026年11月3日

上次提交的符合 QC 标准的更新

2026年10月28日

最后验证

2026年10月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅