Literature DB >> 20071999

Pharmacokinetic/pharmacodynamic modeling of the antiretroviral activity of the CCR5 antagonist Vicriviroc in treatment experienced HIV-infected subjects (ACTG protocol 5211).

Keith W Crawford1, Chonghua Li, Anther Keung, Zhaohui Su, Michael D Hughes, Wayne Greaves, Daniel Kuritzkes, Roy Gulick, Charles Flexner.   

Abstract

OBJECTIVE: This substudy of AIDS Clinical Trials Group (ACTG) Protocol 5211 explored the relationship between antiretroviral effect and plasma concentrations of vicriviroc, an investigational CCR5 antagonist for HIV infection.
METHODS: Eighty-six treatment-experienced subjects failing their current antiretroviral regimens were randomized to add vicriviroc 5, 10, or 15 mg once daily or placebo for 2 weeks. Beyond week 2, subjects were changed to optimized background antiretroviral treatment while continuing vicriviroc or placebo. Plasma samples collected at weeks 2 and 8 were assayed for vicriviroc concentrations and combined with vicriviroc concentration data from 110 seronegatives enrolled in 5 phase 1 studies. An inhibitory Emax model was used to assess pharmacokinetic (PK)/pharmacodynamic relationships and recursive partitioning was applied to determine the breakpoint in vicriviroc PK parameters associated with virologic suppression.
RESULTS: A 2-compartment model was fitted to the drug concentration data. At week 2, a higher vicriviroc Cmin was associated with a greater mean drop in HIV RNA (viral load) and a higher percentage of subjects experiencing a >1 log10 copies/mL drop in viral load. In subjects with Cmin > 54 ng/mL, the mean viral load decrease was 1.35 log10 copies/mL vs. 0.76 log10 with Cmin < 54 ng/mL (P = 0.003, Student t test). At this Cmin breakpoint, 70% of subjects with the higher Cmin had a >1 log drop in HIV RNA, compared with 44% with a lower Cmin (P = 0.048, Fisher exact test). Similar results were seen with an area under the curve breakpoint of 1460 ng h/mL. At weeks 16 and 24, all vicriviroc-treated subjects experienced better viral load responses than placebo recipients, but there was no apparent relationship between PK and change in viral load among these vicriviroc-treated subjects.
CONCLUSIONS: There was a positive correlation between vicriviroc Cmin, area under the curve, and viral load changes at week 2 in treatment-experienced HIV-infected subjects receiving no other new active antiretroviral drugs. This correlation did not persist beyond week 16, probably because treatment response at that point also depended on having other active drugs in the regimen.

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Year:  2010        PMID: 20071999      PMCID: PMC2862681          DOI: 10.1097/QAI.0b013e3181c9caac

Source DB:  PubMed          Journal:  J Acquir Immune Defic Syndr        ISSN: 1525-4135            Impact factor:   3.731


  28 in total

1.  Mapping resistance to the CCR5 co-receptor antagonist vicriviroc using heterologous chimeric HIV-1 envelope genes reveals key determinants in the C2-V5 domain of gp120.

Authors:  Robert A Ogert; Lisa Wojcik; Catherine Buontempo; Lei Ba; Peter Buontempo; Robert Ralston; Julie Strizki; John A Howe
Journal:  Virology       Date:  2008-01-10       Impact factor: 3.616

2.  Antiviral activity, pharmacokinetics, and dose response of the HIV-1 integrase inhibitor GS-9137 (JTK-303) in treatment-naive and treatment-experienced patients.

Authors:  Edwin DeJesus; Daniel Berger; Martin Markowitz; Calvin Cohen; Trevor Hawkins; Peter Ruane; Richard Elion; Charles Farthing; Lijie Zhong; Andrew K Cheng; Damian McColl; Brian P Kearney
Journal:  J Acquir Immune Defic Syndr       Date:  2006-09       Impact factor: 3.731

3.  Reduced maximal inhibition in phenotypic susceptibility assays indicates that viral strains resistant to the CCR5 antagonist maraviroc utilize inhibitor-bound receptor for entry.

Authors:  Mike Westby; Caroline Smith-Burchnell; Julie Mori; Marilyn Lewis; Michael Mosley; Mark Stockdale; Patrick Dorr; Giuseppe Ciaramella; Manos Perros
Journal:  J Virol       Date:  2006-12-20       Impact factor: 5.103

4.  Phase 2 study of the safety and efficacy of vicriviroc, a CCR5 inhibitor, in HIV-1-Infected, treatment-experienced patients: AIDS clinical trials group 5211.

Authors:  Roy M Gulick; Zhaohui Su; Charles Flexner; Michael D Hughes; Paul R Skolnik; Timothy J Wilkin; Robert Gross; Amy Krambrink; Eoin Coakley; Wayne L Greaves; Andrew Zolopa; Richard Reichman; Catherine Godfrey; Martin Hirsch; Daniel R Kuritzkes
Journal:  J Infect Dis       Date:  2007-06-05       Impact factor: 5.226

5.  Identification of human liver cytochrome P450 enzymes involved in biotransformation of vicriviroc, a CCR5 receptor antagonist.

Authors:  Anima Ghosal; Ragu Ramanathan; Yuan Yuan; Neil Hapangama; Swapan K Chowdhury; Narendra S Kishnani; Kevin B Alton
Journal:  Drug Metab Dispos       Date:  2007-09-07       Impact factor: 3.922

6.  Phase II study of vicriviroc versus efavirenz (both with zidovudine/lamivudine) in treatment-naive subjects with HIV-1 infection.

Authors:  Raphael J Landovitz; Jonathan B Angel; Christian Hoffmann; Heinz Horst; Milos Opravil; Jianmin Long; Wayne Greaves; Gerd Fätkenheuer
Journal:  J Infect Dis       Date:  2008-10-15       Impact factor: 5.226

7.  Molecular interactions of CCR5 with major classes of small-molecule anti-HIV CCR5 antagonists.

Authors:  Rama Kondru; Jun Zhang; Changhua Ji; Tara Mirzadegan; David Rotstein; Surya Sankuratri; Marianna Dioszegi
Journal:  Mol Pharmacol       Date:  2007-12-20       Impact factor: 4.436

8.  The impact of HIV tropism on decreases in CD4 cell count, clinical progression, and subsequent response to a first antiretroviral therapy regimen.

Authors:  Laura Waters; Sundhiya Mandalia; Paul Randell; Adrian Wildfire; Brian Gazzard; Graeme Moyle
Journal:  Clin Infect Dis       Date:  2008-05-15       Impact factor: 9.079

9.  In vivo emergence of vicriviroc resistance in a human immunodeficiency virus type 1 subtype C-infected subject.

Authors:  Athe M N Tsibris; Manish Sagar; Roy M Gulick; Zhaohui Su; Michael Hughes; Wayne Greaves; Mani Subramanian; Charles Flexner; Françoise Giguel; Kay E Leopold; Eoin Coakley; Daniel R Kuritzkes
Journal:  J Virol       Date:  2008-05-21       Impact factor: 5.103

10.  Maraviroc for previously treated patients with R5 HIV-1 infection.

Authors:  Roy M Gulick; Jacob Lalezari; James Goodrich; Nathan Clumeck; Edwin DeJesus; Andrzej Horban; Jeffrey Nadler; Bonaventura Clotet; Anders Karlsson; Michael Wohlfeiler; John B Montana; Mary McHale; John Sullivan; Caroline Ridgway; Steve Felstead; Michael W Dunne; Elna van der Ryst; Howard Mayer
Journal:  N Engl J Med       Date:  2008-10-02       Impact factor: 91.245

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  5 in total

Review 1.  Therapeutic implications of chemokine-mediated pathways in atherosclerosis: realistic perspectives and utopias.

Authors:  Stavros Apostolakis; Virginia Amanatidou; Demetrios A Spandidos
Journal:  Acta Pharmacol Sin       Date:  2010-08-16       Impact factor: 6.150

2.  From in vitro EC₅₀ to in vivo dose-response for antiretrovirals using an HIV disease model. Part II: application to drug development.

Authors:  Jing Fang; Pravin R Jadhav
Journal:  J Pharmacokinet Pharmacodyn       Date:  2012-07-08       Impact factor: 2.745

Review 3.  Targeting CCR5 for anti-HIV research.

Authors:  W-G Gu; X-Q Chen
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2014-06-11       Impact factor: 3.267

4.  Phase 1 Safety and Pharmacokinetics Study of MK-2048/Vicriviroc (MK-4176)/MK-2048A Intravaginal Rings.

Authors:  Craig J Hoesley; Beatrice A Chen; Peter L Anderson; Charlene S Dezzutti; Julie Strizki; Carol Sprinkle; Faye Heard; Jose Bauermeister; Wayne Hall; Cindy Jacobson; Jennifer Berthiaume; Ashley Mayo; Holly Gundacker; Nicola Richardson-Harman; Jeanna Piper
Journal:  Clin Infect Dis       Date:  2019-03-19       Impact factor: 9.079

Review 5.  Closing the door to human immunodeficiency virus.

Authors:  Yuanxi Kang; Jia Guo; Zhiwei Chen
Journal:  Protein Cell       Date:  2013-03-12       Impact factor: 14.870

  5 in total

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