Results 11 to 20 of about 3,975 (165)

Effect of ABCB1 most frequent polymorphisms on the accumulation of bictegravir in recombinant HEK293 cell lines

open access: yesScientific Reports
Bictegravir, a key second-generation integrase strand transfer inhibitor in the treatment of HIV, is subject to active efflux transport mediated by ABCB1 (P-glycoprotein).
Julien De Greef   +9 more
doaj   +2 more sources

A New Combined Antiretroviral Therapy In Adolescents With HIV: Bictegravir/Emtricitabine/Tenofovir Alafenamide

open access: yesJournal of Global Antimicrobial Resistance
AIM: We aimed to evaluate the treatment response and side effect profile of bictegravir as initial therapy in HIV-naive adolescents. BACKGROUND: Bictegravir is a potent integrase helicase transfer inhibitor with a high genetic barrier to resistance ...
Neslihan Mete Atasever   +4 more
doaj   +2 more sources

Exploring the pharmacokinetic mechanisms that affect bictegravir exposure during pregnancy. [PDF]

open access: yesJ Antimicrob Chemother
Contains fulltext : 331974.pdf (Publisher’s version ) (Open Access)INTRODUCTION: Pregnancy is associated with physiological changes, resulting in altered pharmacokinetics, which may impact antiretroviral drug exposure.
van der Wekken-Pas L   +10 more
europepmc   +2 more sources

Bictegravir/emtricitabine/tenofovir alafenamide in clinical practice for people with HIV: final 24-month effectiveness and safety outcomes in key populations in the observational BICSTaR cohort

open access: yesHIV Research & Clinical Practice
Background: BICtegravir Single Tablet Regimen (BICSTaR) is an observational cohort study evaluating the effectiveness and safety of bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) in treatment-naïve (TN) and treatment-experienced (TE) people ...
Benoit Trottier   +18 more
doaj   +3 more sources

Physiologically‐Based Pharmacokinetic Modeling to Support the Clinical Management of Drug–Drug Interactions With Bictegravir [PDF]

open access: yes, 2021
Bictegravir is equally metabolized by cytochrome P450 (CYP)3A and uridine diphosphate-glucuronosyltransferase (UGT)1A1. Drug–drug interaction (DDI) studies were only conducted for strong inhibitors and inducers, leading to some uncertainty whether ...
Marzolini, C.   +8 more
core   +1 more source

Antiretroviral drugs efavirenz, dolutegravir and bictegravir dysregulate blood-brain barrier integrity and function

open access: yesFrontiers in Pharmacology, 2023
The implementation of combined antiretroviral therapy (cART) significantly reduces the mortality associated with human immunodeficiency virus (HIV) infection.
Chang Huang   +2 more
doaj   +1 more source

Physiologically‐Based Pharmacokinetic Modeling Combined with Swiss HIV Cohort Study Data Supports No Dose Adjustment of Bictegravir in Elderly Individuals Living With HIV [PDF]

open access: yes, 2021
Clinical studies in aging people living with HIV (PLWH) are sparse for the novel integrase inhibitor bictegravir, leading to some uncertainty about dosing recommendations for elderly PLWH.
Decosterd, L.A.   +14 more
core   +1 more source

Assessment of Gastrointestinal Adverse Effects during the First Six Months of “Biktarvy” Antiretroviral Therapy: Age-Related Patterns and Their Relation with Changes of 5 kg Weight Loss/Gain in the Initial Treatment Period

open access: yesDiseases, 2023
Background: The battle against HIV has led to the development of antiretroviral therapy (ART), including BIKTARVY®, which combines three potent agents.
Madalina-Ianca Suba   +7 more
doaj   +1 more source

Population pharmacokinetics of bictegravir in real-world people with HIV. [PDF]

open access: yesJ Antimicrob Chemother
Bictegravir is an integrase strand transfer inhibitor widely prescribed due to its good efficacy and safety profile. Its pharmacokinetic (PK) profile has not been described in real-world settings yet.
Ekobena P   +9 more
europepmc   +2 more sources

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