نتایج جستجو برای: rilpivirine

تعداد نتایج: 396  

Journal: :Molecular bioSystems 2016
Bilal Nizami Dominique Sydow Gerhard Wolber Bahareh Honarparvar

Regardless of advances in anti-HIV therapy, HIV infection remains an immense challenge due to the rapid onset of mutation instigating drug resistance. Rilpivirine is a second generation di-aryl pyrimidine (DAPY) derivative, known to effectively inhibit wild-type (WT) as well as various mutant HIV-1 reverse transcriptase (RT). In this study, a cumulative 240 ns of molecular dynamic (MD) simulati...

Journal: :Biochemical pharmacology 2012
Erik De Clercq

The triple-drug once-daily combination pill containing tenofovir, emtricitabine and rilpivirine for HIV treatment was launched in 2011, both in the USA (Complera) and the E.U. (Eviplera). The active ingredients of Complera or Eviplera are the nucleotide reverse transcriptase inhibitor (NtRTI) tenofovir, the nucleoside reverse transcriptase inhibitor (NRTI) emtricitabine, and the non-nucleoside ...

Journal: :Lancet 2011
Calvin J Cohen Jaime Andrade-Villanueva Bonaventura Clotet Jan Fourie Margaret A Johnson Kiat Ruxrungtham Hao Wu Carmen Zorrilla Herta Crauwels Laurence T Rimsky Simon Vanveggel Katia Boven

BACKGROUND The non-nucleoside reverse transcriptase inhibitor (NNRTI), rilpivirine (TMC278; Tibotec Pharmaceuticals, County Cork, Ireland), had equivalent sustained efficacy to efavirenz in a phase 2b trial in treatment-naive patients infected with HIV-1, but fewer adverse events. We aimed to assess non-inferiority of rilpivirine to efavirenz in a phase 3 trial with common background nucleoside...

Journal: :The Journal of antimicrobial chemotherapy 2014
H Jeulin M Foissac L Boyer N Agrinier P Perrier A Kennel A Velay F Goehringer S Henard C Rabaud T May E Schvoerer

OBJECTIVES To assess the prevalence of resistance to rilpivirine and mutations at position 138 in reverse transcriptase and to identify associated epidemiological and biological characteristics. METHODS This retrospective study included 238 patients with available HIV-1 nucleotide sequences analysed at the Laboratory of Virology at the University Hospital of Nancy between January 2011 and Jun...

2011
Nathan Ford Janice Lee Isabelle Andrieux-Meyer Alexandra Calmy

The vast majority of people living with human immunodeficiency virus (HIV)/acquired immune deficiency syndrome reside in the developing world, in settings characterized by limited health budgets, critical shortages of doctors, limited laboratory monitoring, a substantial burden of HIV in children, and high rates of coinfection, in particular tuberculosis. Therefore, the extent to which new anti...

Journal: :The lancet. HIV 2017
Chloe Orkin Edwin DeJesus Moti Ramgopal Gordon Crofoot Peter Ruane Anthony LaMarca Anthony Mills Bernard Vandercam Joseph de Wet Jürgen Rockstroh Adriano Lazzarin Bart Rijnders Daniel Podzamczer Anders Thalme Marcel Stoeckle Danielle Porter Hui C Liu Andrew Cheng Erin Quirk Devi SenGupta Huyen Cao

BACKGROUND Tenofovir alafenamide, a tenofovir prodrug, results in 90% lower tenofovir plasma concentrations than does tenofovir disproxil fumarate, thereby minimising bone and renal risks. We investigated the efficacy, safety, and tolerability of switching to a single-tablet regimen containing rilpivirine, emtricitabine, and tenofovir alafenamide compared with remaining on rilpivirine, emtricit...

Journal: :Biochemical pharmacology 2013
Devinder Sharma Aik Jiang Lau Matthew A Sherman Thomas K H Chang

Rilpivirine and etravirine are second generation non-nucleoside reverse transcriptase inhibitors approved recently by the United States Food and Drug Administration for the treatment of human immunodeficiency virus-1 infection. Pregnane X receptor (PXR) is a member of the superfamily of nuclear receptors that regulate the expression of various genes controlling diverse biological functions. The...

Journal: :Lancet 2018
Josep M Llibre Chien-Ching Hung Cynthia Brinson Francesco Castelli Pierre-Marie Girard Lesley P Kahl Elizabeth A Blair Kostas Angelis Brian Wynne Kati Vandermeulen Mark Underwood Kim Smith Martin Gartland Michael Aboud

BACKGROUND Lifelong HIV antiretroviral therapy (ART) has prompted an interest in two-drug regimens to minimise cumulative drug exposure and toxicities. The safety, tolerability, and efficacy of dolutegravir and rilpivirine suggest potential compatibility and effectiveness as a two-drug regimen. We aimed to investigate this two-drug regimen in a phase 3 study. METHODS We identically designed S...

Journal: :Journal of Pharmaceutical Research 2022

A simple, sensitive, specific, accurate, and stability-indicating reversed phase high performance liquid chromatographic method was developed for the simultaneous determination of cabotegravir rilpivirine in injection dosage form, using a Waters Model No.2695 series compact system fitted with Agilent - C18 column (BDS) (150 X 4.6 mm, 5μm) mobile composed 0.01N KH2PO4 buffer (pH: 4.8): acetonitr...

Journal: :BETA : bulletin of experimental treatments for AIDS : a publication of the San Francisco AIDS Foundation 2011
Reilly O'Neal

Two antiretroviral medicines recently came on the scene for people starting HIV treatment for the first time: Rilpivirine (brand name Edurant) won marketing approval in May, and the following August saw approval of Complera, a single-pill once-daily regimen that joins rilpivirine with two other drugs. This article explains the science behind rilpivirine and Complera and how these drugs measure ...

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