Results 91 to 100 of about 901 (171)

A Stability-indicating High Performance Liquid Chromatographic Method for the Determination of Cobicistat [PDF]

open access: yes, 2015
A new reverse phase – high performance liquid chromatography (RP-HPLC) have been developed and validated for theestimation of Cobicistat in bulk drug and pharmaceutical dosage form.
KALYANI, K. (K), ANURADHA, V. (V)
core  

Inhibition of human cytochromes P450 in vitro by ritonavir and cobicistat

open access: yes, 2017
Objectives Ritonavir and cobicistat are strong inhibitors of human cytochrome P450-3A (CYP3A) isoforms, and are used clinically as pharmacokinetic boosting agents for other antiretroviral drugs. Data reported by the manufacturer suggest
Gerd Mikus   +4 more
core   +1 more source

Efficacy and safety of elvitegravir/cobicistat/emtricitabine/tenofovir alafenamide in Asian participants with human immunodeficiency virus 1 infection: A sub-analysis of phase 3 clinical trials

open access: yesHIV Research & Clinical Practice, 2019
Background: The efficacy and safety of a single tablet regimen (STR) of elvitegravir/cobicistat/emtricitabine/tenofovir alafenamide (E/C/F/TAF) was analyzed in Phase 3 clinical trials in antiretroviral therapy (ART)-naive and ART-experienced Asian ...
Yeon-Sook Kim   +17 more
doaj   +1 more source

Pharmacokinetic interaction of riociguat and antiretroviral combination regimens in HIV-1-infected adults

open access: yesPulmonary Circulation, 2019
Riociguat, a first-in-class soluble guanylate cyclase stimulator, is approved for the treatment of pulmonary arterial hypertension (PAH), a serious potential complication of human immunodeficiency virus (HIV) infection. This open-label study investigated
Edwin DeJesus   +7 more
doaj   +1 more source

NEW ANALYTICAL METHOD VALIDATION REPORT AND FORCED DEGRADATION STUDIES FOR ASSAY OF ELVITEGRAVIR, TENOFOVIR, EMTRICITABINE AND COBICISTAT BY RP-UPLC

open access: yes, 2017
The main aim of the present work is to develop and validate a simple, specific, efficient, accurate, and precise stability-indicating rapid reversed phase ultra performance liquid chromatographic method is developed for the simultaneous determination of ...
K. Kranthi Kiran*, Dr. A. Srinivasa Rao, Prof. D. Gowri Sankar
core   +1 more source

Choice of the initial antiretroviral treatment for HIV-positive individuals in the era of integrase inhibitors.

open access: yesPLoS ONE, 2019
BackgroundWe aimed to describe the most frequently prescribed initial antiretroviral therapy (ART) regimens in recent years in HIV-positive persons in the Cohort of the Spanish HIV/AIDS Research Network (CoRIS) and to investigate factors associated with ...
Belén Alejos   +9 more
doaj   +1 more source

Validation of a LC-MS/MS Assay for Rapid and Simultaneous Quantification of Cobicistat and Venetoclax in Human Plasma and Serum [PDF]

open access: yes
Measuring cobicistat and venetoclax concentrations in human plasma and serum facilitates therapeutic drug monitoring (TDM) and pharmacokinetic (PK) boosting studies.
Oude Munnink, T. H.; id_orcid   +5 more
core   +1 more source

Pharmacokinetic interaction between single and multiple doses of darunavir, in combination with cobicistat or ritonavir, and single-dose dabigatran etexilate in healthy adults

open access: yesAAPS Open
Objective Darunavir (DRV) is a P-glycoprotein (P-gp) inhibitor. Dabigatran etexilate, prodrug of the anticoagulant dabigatran, is a P-gp probe substrate. This study evaluated the effect of single and multiple doses of DRV, coadministered with cobicistat (
Sandy Van Hemelryck   +5 more
doaj   +1 more source

DEVELOPMENT AND VALIDATION OF A NEW RP-HPLC METHOD FOR SIMULTANEOUS ESTIMATION OF EMTRICITABINE TENOFOVIR COBICISTAT ELVITEGRAVIR AND ITS COMPARISION WITH A REPORTED METHOD

open access: yes, 2017
A new stability indicating RP HPLC method has been developed and validated for simultaneous estimation of Emtricitabine, Tenofovir, Cobicistat and Elvitegravir in bulk and dosage forms. The method involves separation on Kromasil C18 column (250mm x 4.6mm
Mangamma.Kuna*, Gowri Sankar Dannana and S.V.U.M.Prasad
core   +1 more source

Pharmacokinetic boosting of olaparib: Study protocol of a multicentre, open-label, randomised, non-inferiority trial (PROACTIVE-B)

open access: yesContemporary Clinical Trials Communications
Background: Pharmacokinetic (PK) boosting is the intentional use of a drug-drug interaction to enhance systemic drug exposure. PK boosting of the anticancer drug olaparib, a CYP3A-substrate, has the potential to reduce PK variability, side effects and ...
Joanneke K. Overbeek   +16 more
doaj   +1 more source

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