Pharmacokinetic modelling of darunavir/ritonavir dose reduction (800/100 to 400/100 mg once daily) in a darunavir/ritonavir-containing regimen in virologically suppressed HIV-infected patients: ANRS 165 DARULIGHT sub-study
Author(s) -
Minh Patrick Lê,
MarieLaure Chaix,
Sylvie Chevret,
Julie Bertrand,
F. Raffi,
Sébastien Gallien,
El Mountacer Billah El Abbassi,
Christine Katlama,
Pierre Delobel,
Yazdan Yazdanpanah,
Juliette Saillard,
JeanMichel Molina,
Gilles Peytavin,
Diane Ponscarme,
C. Lascoux,
Pierre Marie Girard,
A. Rami,
Anne Simon,
Roland Tubiana,
Claudine Duvivier,
Vincent Jeantils,
D Loreillard,
Isabelle PoizotMartin,
Louis Bernard,
Guillaume Gras,
Clotilde Allavena,
Eric Billaud,
Sabelline Bouchez,
Nancy Hall,
Véronique Reliquet,
P. de Truchis,
Isabelle Charreau,
L Bocquet,
Vincent Le Moing,
G Point,
Ebrahim Abassi,
Pierre Tattevin,
S. Couffin-Cadiergues,
Isabelle Madelaine,
Alpha Diallo,
Séverine Gibowski
Publication year - 2018
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dky193
Subject(s) - darunavir , ritonavir , pharmacokinetics , regimen , pharmacology , medicine , bioequivalence , virology , viral load , human immunodeficiency virus (hiv) , antiretroviral therapy
In the ANRS 165 DARULIGHT study (NCT02384967) carried out in HIV-infected patients, the use of a darunavir/ritonavir-containing regimen with a switch to a reduced dose of darunavir maintained virological efficacy (≤50 copies/mL) for 48 weeks with a good safety profile.
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