Literature DB >> 22174038

Once daily maraviroc 300 mg or 150 mg in combination with ritonavir-boosted darunavir 800/100 mg.

Chinyere Okoli1, Marco Siccardi, Sathish Thomas-William, Ngozi Dufty, Kirstin Khonyongwa, Jonathan Ainsworth, John Watson, Roseanne Cook, Kate Gandhi, Geraldine Hickinbottom, Andrew Owen, Stephen Taylor.   

Abstract

OBJECTIVES: To describe the pharmacokinetics of maraviroc when dosed at 150 or 300 mg once daily with 800/100 mg of darunavir/ritonavir.
METHODS: A retrospective case-note review of HIV-infected adults taking maraviroc was conducted. Patients on a maraviroc-based regimen for a minimum of 5 weeks were grouped as receiving: (i) 300 mg of maraviroc twice daily with 245 mg of tenofovir/200 mg of emtricitabine; (ii) 300 mg of maraviroc once daily with 800/100 mg of darunavir/ritonavir once daily; and (iii) 150 mg of maraviroc once daily with 800/100 mg of darunavir/ritonavir once daily. C(trough) and C(peak) data were collected at 2, 12 or 24 h post-dose.
RESULTS: Sixty-six patients were included, providing 115 samples. The median (IQR) C(peak) was 378 (350-640) ng/mL for 300 mg of maraviroc twice daily with 245 mg of tenofovir/200 mg of emtricitabine (n=9), 728 (378-935) ng/mL for 300 mg of maraviroc once daily with darunavir/ritonavir (n=29) and 364 (104-624) ng/mL for 150 mg of maraviroc once daily with darunavir/ritonavir (n=2; P=0.24). The median (IQR) C(trough) was 46 (33-61) ng/mL for 300 mg of maraviroc twice daily with 245 mg of tenofovir/200 mg of emtricitabine (n=12), 70 (49-97) ng/mL for 300 mg of maraviroc once daily with darunavir/ritonavir (n=34) and 43 (35-55) ng/mL for 150 mg of maraviroc once daily with darunavir/ritonavir (n=17; P=0.001). The maraviroc C(trough) in black patients (n=34) was 61 (45-110) ng/mL and in white patients (n=29) it was 49 (42-70) ng/mL (P=0.04). The C(peak) in black patients (n=20) was 800 (397-1060) ng/mL versus 387 (336-723) ng/mL in white patients (n=20; P=0.02).
CONCLUSIONS: Once daily coadministration of 300 mg of maraviroc with 800/100 mg of darunavir/ritonavir was well tolerated and had favourable pharmacokinetics when compared with 300 mg of maraviroc twice daily with 245 mg of tenofovir/200 mg of emtricitabine. A 24% higher C(trough) and 107% higher C(peak) was seen in black patients compared with white patients.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 22174038     DOI: 10.1093/jac/dkr493

Source DB:  PubMed          Journal:  J Antimicrob Chemother        ISSN: 0305-7453            Impact factor:   5.790


  12 in total

1.  CYP3A5 genotype impacts maraviroc concentrations in healthy volunteers.

Authors:  Yanhui Lu; Edward J Fuchs; Craig W Hendrix; Namandjé N Bumpus
Journal:  Drug Metab Dispos       Date:  2014-08-12       Impact factor: 3.922

2.  CSF inflammatory markers and neurocognitive function after addition of maraviroc to monotherapy darunavir/ritonavir in stable HIV patients: the CINAMMON study.

Authors:  T J Barber; A Imaz; M Boffito; J Niubó; A Pozniak; R Fortuny; J Alonso; N Davies; S Mandalia; D Podzamczer; B Gazzard
Journal:  J Neurovirol       Date:  2017-12-26       Impact factor: 2.643

3.  Virologic response, early HIV-1 decay, and maraviroc pharmacokinetics with the nucleos(t)ide-free regimen of maraviroc plus darunavir/ritonavir in a pilot study.

Authors:  Babafemi Taiwo; Edward P Acosta; Patrick Ryscavage; Baiba Berzins; Darlene Lu; Jay Lalezari; Jose Castro; Oluwatoyin Adeyemi; Daniel R Kuritzkes; Joseph J Eron; Athe Tsibris; Susan Swindells
Journal:  J Acquir Immune Defic Syndr       Date:  2013-10-01       Impact factor: 3.731

4.  Less Bone Loss With Maraviroc- Versus Tenofovir-Containing Antiretroviral Therapy in the AIDS Clinical Trials Group A5303 Study.

Authors:  Babafemi O Taiwo; Ellen S Chan; Carl J Fichtenbaum; Heather Ribaudo; Athe Tsibris; Karin L Klingman; Joseph J Eron; Baiba Berzins; Kevin Robertson; Alan Landay; Igho Ofotokun; Todd Brown
Journal:  Clin Infect Dis       Date:  2015-06-09       Impact factor: 9.079

5.  Maraviroc Pharmacokinetics in HIV-1-Infected Pregnant Women.

Authors:  Angela Colbers; Brookie Best; Stein Schalkwijk; Jiajia Wang; Alice Stek; Carmen Hidalgo Tenorio; David Hawkins; Graham Taylor; Regis Kreitchmann; Sandra Burchett; Annette Haberl; Kabamba Kabeya; Marjo van Kasteren; Elizabeth Smith; Edmund Capparelli; David Burger; Mark Mirochnick
Journal:  Clin Infect Dis       Date:  2015-07-22       Impact factor: 9.079

6.  Pharmacokinetic interaction between maraviroc and fosamprenavir-ritonavir: an open-label, fixed-sequence study in healthy subjects.

Authors:  Manoli Vourvahis; Anna Plotka; Laure Mendes da Costa; Annie Fang; Jayvant Heera
Journal:  Antimicrob Agents Chemother       Date:  2013-09-30       Impact factor: 5.191

Review 7.  Clinical pharmacokinetics of antiretroviral drugs in older persons.

Authors:  John C Schoen; Kristine M Erlandson; Peter L Anderson
Journal:  Expert Opin Drug Metab Toxicol       Date:  2013-03-20       Impact factor: 4.481

Review 8.  Dosing antiretroviral medication when crossing time zones: a review.

Authors:  Joseph M Lewis; Alain Volny-Anne; Catriona Waitt; Marta Boffito; Saye Khoo
Journal:  AIDS       Date:  2016-01       Impact factor: 4.177

9.  French 2013 guidelines for antiretroviral therapy of HIV-1 infection in adults.

Authors:  Bruno Hoen; Fabrice Bonnet; Constance Delaugerre; Pierre Delobel; Cécile Goujard; Marianne L'Hénaff; Renaud Persiaux; David Rey; Christine Rouzioux; Anne-Marie Taburet; Philippe Morlat
Journal:  J Int AIDS Soc       Date:  2014-06-17       Impact factor: 5.396

10.  Use of in vitro to in vivo extrapolation to predict the optimal strategy for patients switching from efavirenz to maraviroc or nevirapine.

Authors:  Alessandro Schipani; David Back; Andrew Owen; Gerry Davies; Saye Khoo; Marco Siccardi
Journal:  Clin Pharmacokinet       Date:  2015-01       Impact factor: 5.577

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.