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Volumn 26, Issue 8, 2010, Pages 841-845

Short communication: Comparable safety and efficacy with once-daily versus twice-daily dosing of lopinavir/ritonavir tablets with emtricitabine + tenofovir DF in antiretroviral-naïve, HIV type 1-infected subjects: 96 week final results of the randomized trial M05-730

Author keywords

[No Author keywords available]

Indexed keywords

EMTRICITABINE PLUS TENOFOVIR DISOPROXIL; LOPINAVIR PLUS RITONAVIR; VIRUS RNA; ADENINE; ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT; DEOXYCYTIDINE; DRUG COMBINATION; EMTRICITABINE; LOPINAVIR; PHOSPHONIC ACID DERIVATIVE; PYRIMIDINONE DERIVATIVE; RITONAVIR; TENOFOVIR;

EID: 77955631576     PISSN: 08892229     EISSN: None     Source Type: Journal    
DOI: 10.1089/aid.2009.0307     Document Type: Article
Times cited : (18)

References (10)
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    • Walmsley, S.1    Bernstein, B.2    King, M.3
  • 2
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    • Seven-year efficacy of a lopinavir/ritonavir-based regimen in antiretroviralnäve HIV-1-infected patients
    • Murphy R, da Silva BA, Hicks CB, et al.: Seven-year efficacy of a lopinavir/ritonavir-based regimen in antiretroviralnäve HIV-1-infected patients. HIV Clin Trials 2008; 9:1-10.
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  • 3
    • 0036499067 scopus 로고    scopus 로고
    • Safety and antiviral activity at 48 weeks of lopinavir/ritonavir plus nevirapine and 2 nucleoside reverse-transcriptase inhibitors in human immunodeficiency virus type 1-infected protease inhibitorexperienced patients
    • Benson CA, Deeks SG, Brun SC, et al.: Safety and antiviral activity at 48 weeks of lopinavir/ritonavir plus nevirapine and 2 nucleoside reverse-transcriptase inhibitors in human immunodeficiency virus type 1-infected protease inhibitorexperienced patients. J Infect Dis 2002;185:599-607.
    • (2002) J Infect Dis , vol.185 , pp. 599-607
    • Benson, C.A.1    Deeks, S.G.2    Brun, S.C.3
  • 4
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    • Long-term antiretroviral efficacy and safety of lopinavir/ritonavir HAARTexperienced subjects: 4 year follow-up study
    • Bongiovanni M, Bini T, Capetti A, et al.: Long-term antiretroviral efficacy and safety of lopinavir/ritonavir HAARTexperienced subjects: 4 year follow-up study. AIDS 2005; 19:1934-1936.
    • (2005) AIDS , vol.19 , pp. 1934-1936
    • Bongiovanni, M.1    Bini, T.2    Capetti, A.3
  • 5
    • 9144233476 scopus 로고    scopus 로고
    • Once-daily versus twice-daily lopinavir/ritonavir in antiretroviral-naive HIVpositive patients: A 48-week randomized clinical trial
    • Eron JJ, Feinberg J, Kessler HA, et al.: Once-daily versus twice-daily lopinavir/ritonavir in antiretroviral-naive HIVpositive patients: A 48-week randomized clinical trial. J Infect Dis 2004;189:265-272.
    • (2004) J Infect Dis , vol.189 , pp. 265-272
    • Eron, J.J.1    Feinberg, J.2    Kessler, H.A.3
  • 6
    • 37549066355 scopus 로고    scopus 로고
    • A lopinavir/ ritonavir-based once-daily regimen results in better compliance and is non-inferior to a twice-daily regimen through 96 weeks
    • Molina JM, Podsadecki TJ, Johnson MA, et al.: A lopinavir/ ritonavir-based once-daily regimen results in better compliance and is non-inferior to a twice-daily regimen through 96 weeks. AIDS Res Hum Retroviruses 2007;23: 1505-1514.
    • (2007) AIDS Res Hum Retroviruses , vol.23 , pp. 1505-1514
    • Molina, J.M.1    Podsadecki, T.J.2    Johnson, M.A.3
  • 7
    • 65449165011 scopus 로고    scopus 로고
    • A once-daily lopinavir/ritonavir-based regimen is noninferior to twicedaily dosing and results in similar safety and tolerability in antiretroviral-naive subjects through 48 weeks
    • Gathe J, da Silva BA, Cohen DE, et al.: A once-daily lopinavir/ritonavir- based regimen is noninferior to twicedaily dosing and results in similar safety and tolerability in antiretroviral-naive subjects through 48 weeks. J Acquir Immune Defic Syndr 2009;50:474-481.
    • (2009) J Acquir Immune Defic Syndr , vol.50 , pp. 474-481
    • Gathe, J.1    Da Silva, B.A.2    Cohen, D.E.3
  • 9
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    • Better adherence with once-daily antiretroviral regimens: A meta-analysis
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    • Parienti, J.J.1    Bangsberg, D.R.2    Verdon, R.3    Gardner, E.M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.