BENITIONSClinical Trial Intelligence

Trial Evaluating a First Line Combination Therapy With Raltegravir, Emtricitabine and Tenofovir in HIV-2 Infected Patients

2상 완료 NCT01605890

대상 질환HIV-2 Infection
임상 단계2상
스폰서ANRS, Emerging Infectious Diseases
상태완료
참여자 수30 명
중재(약물)emtricitabine / tenofovir disoproxil fumarate / raltegravir .
시작일2012년 7월
완료일2015년 12월
결과 공개일2018년 7월 20일

요약

The HIV-2 is less common ie 1-2 million people in West Africa. HIV-2 does have the same sensitivity to antiretroviral treatment (ART) compared to HIV-1. The ART strategies that are appropriate for the HIV-1 infection are not as effective for HIV-2. Classical triple therapy including PI is less effective for HIV-2. Also, the choice of ARTs in a second line treatment is limited. The first line optimal treatment has to be defined by a prospective and randomized evaluation of other strategies. The primary endpoint will be adapted to the specificity of the HIV-2 infection. The 1st step is to define, with a phase II clinical trial, whether a strategy including 2 NRTIs and raltegravir, as an alternative strategy to the classical triple therapy, shows an immunovirological response, at least, as good as the one obtained with the triple therapy. The hypothesis is that the low ART response observed in HIV-2 infection is due to a low virological strength of the ARTs used and that the combination of 2 NRTIs and raltegravir should show a therapeutic success of at least 50% at week 48.

Percentage of Participants in Therapeutic Success

at Week 48 · percentage of participants

Raltegravir / Emtricitabine / Tenofovir Disoproxil Fumarate40 percentage of participants

BENITIONS에서 보기 ClinicalTrials.gov 원문 보기

전체 임상

이 페이지는 ClinicalTrials.gov의 공개 데이터를 정리한 것입니다. 의학적 조언이 아니며 투자 권유나 자문도 아닙니다. 반드시 전문의와 상담하세요.