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临床试验/CTIS2022-502127-22-00
CTIS2022-502127-22-00进行中(未招募)1 期

A Phase 3, Randomized, Active-Controlled, Open-Label Clinical Study to Evaluate a Switch to Doravirine/Islatravir (DOR/ISL 100 mg/0.25 mg) Once-Daily in Participants With HIV-1 Who Are Virologically Suppressed on Antiretroviral Therapy - MK-8591A-051

Merck Sharp & Dohme LLC0 个研究点目标入组 501 人开始时间: 2022年12月19日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
501

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 65+(—)
性别
All

入选标准

  • Is HIV-1 positive with plasma HIV-1 RNA <50 copies/mL at screening, Has been receiving continuous, stable oral 2-drug or 3-drug combination (± pharmacokinetic (PK) booster) ART with documented viral suppression (HIV-1 RNA <50 copies/mL) for =3 consecutive months prior to providing documented informed consent and has no history of prior virologic treatment failure on any past or current regimen, Female is not a participant of childbearing potential (POCBP); or if a POCBP uses an acceptable contraceptive method or abstains from penile-vaginal intercourse as their preferred and usual lifestyle; has a negative highly sensitive pregnancy test; and whose medical history, menstrual history, and recent sexual activity has been reviewed by the investigator

排除标准

  • Has human immunodeficiency virus type 2 (HIV-2) infection, Has a documented or known virologic resistance to DOR, Has hypersensitivity or other contraindication to any of the components of the study interventions as determined by the investigator, Has a diagnosis of an active acquired immunodeficiency syndrome (AIDS)-defining opportunistic infection within 30 days prior to screening, Has active hepatitis B virus (HBV) infection, Has chronic hepatitis C virus (HCV) infection consistent with cirrhosis, Has a =5 years prior history of malignancy, Is taking or is anticipated to require systemic immunosuppressive therapy, immune modulators, or strong and moderate cytochrome P450 3A (CYP3A) inducers, Has taken long-acting HIV therapy at any time, Is currently participating in or has participated in a clinical study and received (or is receiving) an investigational compound or device from 45 days prior to Day 1 through the study treatment period

研究者

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