Literature DB >> 9371346

Exposure-response relationships for saquinavir, zidovudine, and zalcitabine in combination therapy.

G F Vanhove1, J M Gries, D Verotta, L B Sheiner, R Coombs, A C Collier, T F Blaschke.   

Abstract

The relationship of CD4+ cell response, level of RNA in plasma, and quantitative peripheral blood mononuclear cell (PBMC) titer to apparent drug exposure was investigated by using data from AIDS Clinical Trial Group protocol 229, a multicenter randomized study. Patients received either saquinavir, zalcitabine, or a combination of both, along with open-label zidovudine. Approximately 100 patients were enrolled in each arm, and the primary study duration was 24 weeks. Individual drug exposure, the area under the concentration-time curve, was estimated by using population-based pharmacokinetic methods. Response was defined as the maximum increase in CD4+ cell count or the maximum decrease in RNA in plasma or PBMC titer adjusted for baseline CD4+ cell count, RNA in plasma, and PBMC titer, respectively. Regression of responses on exposure demonstrated an exposure effect for saquinavir which was significant for the maximum increase in CD4+ cell count and the decrease in RNA in plasma. For the PBMC titer, no significant relationship could be demonstrated but the results suggested a trend similar to that of the other response variables. For all three response variables, the slope of the saquinavir exposure response was greater with the triple combination (saquinavir, zidovudine, and zalcitabine) than with the combination of saquinavir and zidovudine, suggesting possible synergism between saquinavir and zalcitabine.

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Year:  1997        PMID: 9371346      PMCID: PMC164141     

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  10 in total

1.  Pharmacokinetics of saquinavir, zidovudine, and zalcitabine in combination therapy.

Authors:  G F Vanhove; H Kastrissios; J M Gries; D Verotta; K Park; A C Collier; K Squires; L B Sheiner; T F Blaschke
Journal:  Antimicrob Agents Chemother       Date:  1997-11       Impact factor: 5.191

2.  Human immunodeficiency virus type 1 quantitative cell microculture as a measure of antiviral efficacy in a multicenter clinical trial.

Authors:  S A Fiscus; V DeGruttola; P Gupta; D A Katzenstein; W A Meyer; M L LoFaro; M Katzman; M V Ragni; P S Reichelderfer; R W Coombs
Journal:  J Infect Dis       Date:  1995-02       Impact factor: 5.226

3.  Standardization of sensitive human immunodeficiency virus coculture procedures and establishment of a multicenter quality assurance program for the AIDS Clinical Trials Group. The NIH/NIAID/DAIDS/ACTG Virology Laboratories.

Authors:  F B Hollinger; J W Bremer; L E Myers; J W Gold; L McQuay
Journal:  J Clin Microbiol       Date:  1992-07       Impact factor: 5.948

4.  Concentrations of phosphorylated zidovudine (ZDV) in patient leukocytes do not correlate with ZDV dose or plasma concentrations.

Authors:  B N Stretcher; A J Pesce; J A Murray; P E Hurtubise; W H Vine; P T Frame
Journal:  Ther Drug Monit       Date:  1991-07       Impact factor: 3.681

5.  Rapid and precise quantification of HIV-1 RNA in plasma using a branched DNA signal amplification assay.

Authors:  C Pachl; J A Todd; D G Kern; P J Sheridan; S J Fong; M Stempien; B Hoo; D Besemer; T Yeghiazarian; B Irvine
Journal:  J Acquir Immune Defic Syndr Hum Retrovirol       Date:  1995-04-15

6.  Correlates of zidovudine phosphorylation with markers of HIV disease progression and drug toxicity.

Authors:  B N Stretcher; A J Pesce; P T Frame; K A Greenberg; D S Stein
Journal:  AIDS       Date:  1994-06       Impact factor: 4.177

7.  Human immunodeficiency virus type 1 (HIV-1) inhibitory interactions between protease inhibitor Ro 31-8959 and zidovudine, 2',3'-dideoxycytidine, or recombinant interferon-alpha A against zidovudine-sensitive or -resistant HIV-1 in vitro.

Authors:  V A Johnson; D P Merrill; T C Chou; M S Hirsch
Journal:  J Infect Dis       Date:  1992-11       Impact factor: 5.226

8.  Treatment of human immunodeficiency virus infection with saquinavir, zidovudine, and zalcitabine. AIDS Clinical Trials Group.

Authors:  A C Collier; R W Coombs; D A Schoenfeld; R L Bassett; J Timpone; A Baruch; M Jones; K Facey; C Whitacre; V J McAuliffe; H M Friedman; T C Merigan; R C Reichman; C Hooper; L Corey
Journal:  N Engl J Med       Date:  1996-04-18       Impact factor: 91.245

9.  The effect of high-dose saquinavir on viral load and CD4+ T-cell counts in HIV-infected patients.

Authors:  J M Schapiro; M A Winters; F Stewart; B Efron; J Norris; M J Kozal; T C Merigan
Journal:  Ann Intern Med       Date:  1996-06-15       Impact factor: 25.391

10.  Zidovudine response relationships in early human immunodeficiency virus infection.

Authors:  M Sale; L B Sheiner; P Volberding; T F Blaschke
Journal:  Clin Pharmacol Ther       Date:  1993-11       Impact factor: 6.875

  10 in total
  11 in total

1.  Pharmacological basis for concentration-controlled therapy with zidovudine, lamivudine, and indinavir.

Authors:  T N Kakuda; L M Page; P L Anderson; K Henry; T W Schacker; F S Rhame; E P Acosta; R C Brundage; C V Fletcher
Journal:  Antimicrob Agents Chemother       Date:  2001-01       Impact factor: 5.191

2.  Clinical Pharmacologic Considerations for HIV-1 Protease Inhibitors.

Authors:  Peter L. Anderson; Courtney V. Fletcher
Journal:  Curr Infect Dis Rep       Date:  2001-08       Impact factor: 3.725

Review 3.  Non-linear mixed effects modeling - from methodology and software development to driving implementation in drug development science.

Authors:  Goonaseelan Colin Pillai; France Mentré; Jean-Louis Steimer
Journal:  J Pharmacokinet Pharmacodyn       Date:  2005-11-07       Impact factor: 2.745

4.  Relationships between exposure to saquinavir monotherapy and antiviral response in HIV-positive patients.

Authors:  R Gieschke; B Fotteler; N Buss; J L Steimer
Journal:  Clin Pharmacokinet       Date:  1999-07       Impact factor: 6.447

5.  Clinical and pharmacokinetic data support once-daily low-dose boosted saquinavir (1,200 milligrams saquinavir with 100 milligrams ritonavir) in treatment-naive or limited protease inhibitor-experienced human immunodeficiency virus-infected patients.

Authors:  Ana Marin-Niebla; Luis Fernando Lopez-Cortes; Rosa Ruiz-Valderas; Pompeyo Viciana; Rosario Mata; Alicia Gutierrez; Rosario Pascual; Magdalena Rodriguez
Journal:  Antimicrob Agents Chemother       Date:  2007-03-19       Impact factor: 5.191

6.  Pharmacokinetics of saquinavir, zidovudine, and zalcitabine in combination therapy.

Authors:  G F Vanhove; H Kastrissios; J M Gries; D Verotta; K Park; A C Collier; K Squires; L B Sheiner; T F Blaschke
Journal:  Antimicrob Agents Chemother       Date:  1997-11       Impact factor: 5.191

Review 7.  Updated clinical pharmacologic considerations for HIV-1 protease inhibitors.

Authors:  Peter L Anderson; Courtney V Fletcher
Journal:  Curr HIV/AIDS Rep       Date:  2004-04       Impact factor: 5.071

Review 8.  Therapeutic drug monitoring: an aid to optimising response to antiretroviral drugs?

Authors:  Rob E Aarnoutse; Jonathan M Schapiro; Charles A B Boucher; Yechiel A Hekster; David M Burger
Journal:  Drugs       Date:  2003       Impact factor: 9.546

9.  Estimation of serum-free 50-percent inhibitory concentrations for human immunodeficiency virus protease inhibitors lopinavir and ritonavir.

Authors:  Dean Hickman; Sudthida Vasavanonda; George Nequist; Lynn Colletti; Warren M Kati; Richard Bertz; Ann Hsu; Dale J Kempf
Journal:  Antimicrob Agents Chemother       Date:  2004-08       Impact factor: 5.191

10.  Genomic organization and functional characterization of the human concentrative nucleoside transporter-3 isoform (hCNT3) expressed in mammalian cells.

Authors:  Shuy-Vang Toan; Kenneth K W To; George P H Leung; Maria Olivia de Souza; Jeffrey L Ward; Chung-Ming Tse
Journal:  Pflugers Arch       Date:  2003-09-18       Impact factor: 3.657

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