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Cerebrospinal Fluid Exposure of Efavirenz and Its Major Metabolites When Dosed at 400 mg and 600 mg Once Daily: A Randomized Controlled Trial
Author(s) -
Alan Winston,
Janaki Amin,
Amanda Clarke,
Laura Else,
Alieu Amara,
Andrew Owen,
Tristan Barber,
Heiko Jessen,
Anchalee Avinghsa,
Ploenchan Chetchotisakd,
Saye Khoo,
David A. Cooper,
Sean Emery,
Rebekah Puls,
Dianne Carey,
Kymme Courtney-Vega,
Carlo Dazo,
Anna Donaldson,
Núria Espinosa,
Peeraporn Kaew-on,
Praphan Phanupak,
Kanitta Pussadee,
Louise Tomkins,
Sasiwimol Ubolyam,
Praphan Phanuphak,
Carmen Zedlack,
Brian Gazzard,
Serge Federle,
Sophie Scott,
Borja Mora-Peris,
Ken Legg,
Scott Mullaney,
David Back,
Sujan Dilly Penchala,
Steve Kaye,
Anthony D. Kelleher,
Philip Cunningham,
Kate Merlin,
Julie Yeung,
Ansari Shaik,
Bertha Fsadni,
Alex Carrera,
Melanie Lograsso
Publication year - 2014
Publication title -
clinical infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1093/cid/ciu976
Subject(s) - efavirenz , cerebrospinal fluid , medicine , pharmacokinetics , gastroenterology , reverse transcriptase inhibitor , pharmacology , toxicity , randomized controlled trial , sida , viral load , virology , virus , antiretroviral therapy , viral disease
The optimal penetration of antiretroviral agents into the central nervous system may be a balance between providing adequate drug exposure to inhibit human immunodeficiency virus (HIV) replication while avoiding concentrations associated with neuronal toxicities.

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