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. 2008 Jan 22;52(4):1302–1317. doi: 10.1128/AAC.01324-07

TABLE 7.

Efficacy of Debio-025 in combination with 19 FDA-approved anti-HIV-1 drugs in CEM-SS cellsa

Compound group and compound Synergy vol (nM2 % or nM μM %) Antagonism vol (nM2 % or nM μM %)
Nucleoside RT inhibitors
    3TC 56.9 ± 27.9 7.0 ± 6.6
    ABC 23.6 ± 17.5 22.3 ± 19.6
    AZT 35.6 ± 39.4 43.4 ± 79.1
    d4T 18.8 ± 28.5 10.1 ± 17.2
    ddC 12.2 ± 10.9 15.8 ± 13.7
    ddI 26.8 ± 37.3 20.3 ± 21.9
    FTC 20.0 ± 25.5 9.7 ± 8.5
    TFV 28.1 ± 26.0 12.7 ± 11.1
Nonnucleoside RT inhibitors
    DLV 43.6 ± 37.4 16.4 ± 12.7
    EFV 32.5 ± 34.1 17.7 ± 11.4
    NVP 95.9 ± 63.3 18.0 ± 17.9
Protease inhibitors
    APV 38.8 ± 34.4 0.1 ± 0.2
    ATV 14.8 ± 22.9 44.1 ± 39.7
    IDV 47.8 ± 29.7 24.9 ± 29.0
    LPV 1.3 ± 1.5 30.1 ± 47.7
    NFV 17.5 ± 17.3 38.3 ± 48.4
    RTV 4.6 ± 7.7 20.4 ± 14.4
    SQV 29.3 ± 34.9 26.7 ± 21.4
Fusion inhibitor enfuvirtide 27.8 ± 21.5 0 ± 0
a

HIV-1 strain IIIB-induced CPE; synergy and antagonism volumes were calculated at the 95% confidence level; values are means ± standard deviations from three to six independent determinations.