-
1
-
-
0027323855
-
Amino acid substitutions in HIV-1 reverse transcriptase with corresponding residues from HIV-2. Effect on Kinetic Constants and Inhibition by Non-nucleoside Analogs
-
Bacolla A, Shih C-K, Rose JM, et al. Amino acid substitutions in HIV-1 reverse transcriptase with corresponding residues from HIV-2. Effect on Kinetic Constants and Inhibition by Non-nucleoside Analogs. J Biol Chem 1993; 268: 16571-16577.
-
(1993)
J Biol Chem
, vol.268
, pp. 16571-16577
-
-
Bacolla, A.1
Shih, C.-K.2
Rose, J.M.3
-
2
-
-
0028900894
-
Phase I/II evaluation of nevirapine alone and in combination with zidovudine for infection with human immunodeficiency virus
-
Cheeseman SH, Havlir D, McLaughlin MM, et al. Phase I/II evaluation of nevirapine alone and in combination with zidovudine for infection with human immunodeficiency virus. J Acquir Immune Defic Syndr Hum Retrovirol 1995; 8: 141-151.
-
(1995)
J Acquir Immune Defic Syndr Hum Retrovirol
, vol.8
, pp. 141-151
-
-
Cheeseman, S.H.1
Havlir, D.2
McLaughlin, M.M.3
-
3
-
-
0034541548
-
The VIRGO study: Nevirapine, didanosine and stavudine combination therapy in antiretroviral-naive HIV-1-infected adults
-
Raffi F, Reliquet V, Ferre V, et al. The VIRGO study: nevirapine, didanosine and stavudine combination therapy in antiretroviral-naive HIV-1-infected adults. Antivir Ther 2000; 5: 267-272.
-
(2000)
Antivir Ther
, vol.5
, pp. 267-272
-
-
Raffi, F.1
Reliquet, V.2
Ferre, V.3
-
4
-
-
0032565098
-
A randomized, double-blind trial comparing combinations of nevirapine, didanosine, and zidovudine for HIV-infected patients: The INCAS Trial. Italy, The Netherlands, Canada and Australia Study
-
Montaner JS, Reiss P, Cooper D, et al. A randomized, double-blind trial comparing combinations of nevirapine, didanosine, and zidovudine for HIV-infected patients: the INCAS Trial. Italy, The Netherlands, Canada and Australia Study. JAMA 1998; 279: 930-937.
-
(1998)
JAMA
, vol.279
, pp. 930-937
-
-
Montaner, J.S.1
Reiss, P.2
Cooper, D.3
-
5
-
-
12144285760
-
Pharmacokinetic evaluation and short-term activity of stavudine, nevirapine, and nelfinavir therapy in HIV-1-infected adults
-
Skowron D, Leoung G, Hall DB, et al. Pharmacokinetic evaluation and short-term activity of stavudine, nevirapine, and nelfinavir therapy in HIV-1-infected adults. J Acquir Immune Defic Syndr 2004; 35: 351-358.
-
(2004)
J Acquir Immune Defic Syndr
, vol.35
, pp. 351-358
-
-
Skowron, D.1
Leoung, G.2
Hall, D.B.3
-
6
-
-
0032808202
-
The value of patient-reported adherence to antiretroviral therapy in predicting virologic and immunologic response. California Collaborative Treatment Group
-
Haubrich RH, Little SJ, Currier JS, et al. The value of patient-reported adherence to antiretroviral therapy in predicting virologic and immunologic response. California Collaborative Treatment Group. AIDS 1999; 13: 1099-1107.
-
(1999)
AIDS
, vol.13
, pp. 1099-1107
-
-
Haubrich, R.H.1
Little, S.J.2
Currier, J.S.3
-
7
-
-
3042688704
-
Impact of once- and twice-daily dosing regimens on adherence and overall safety
-
Hawkins T. Impact of once- and twice-daily dosing regimens on adherence and overall safety. AIDS Read 2004; 14: 320-325.
-
(2004)
AIDS Read
, vol.14
, pp. 320-325
-
-
Hawkins, T.1
-
8
-
-
29744439524
-
2NN Study Group. Pharmacokinetics of nevirapine: Once-daily versus twice-daily dosing in the 2NN study
-
Kappelhoff BS, Huitema AD, van Leth F, et al. 2NN Study Group. Pharmacokinetics of nevirapine: once-daily versus twice-daily dosing in the 2NN study. HIV Clin Trials 2005; 6: 254-261.
-
(2005)
HIV Clin Trials
, vol.6
, pp. 254-261
-
-
Kappelhoff, B.S.1
Huitema, A.D.2
van Leth, F.3
-
9
-
-
24044520095
-
Efficacy and safety of once-daily combination therapy with didanosine, lamivudine and nevirapine in antiretroviral-naive HIV-infected patients
-
Ribera E, Rodriguez-Pardo D, Rubio M, et al. Efficacy and safety of once-daily combination therapy with didanosine, lamivudine and nevirapine in antiretroviral-naive HIV-infected patients. Antivir Ther 2005; 10: 605-614.
-
(2005)
Antivir Ther
, vol.10
, pp. 605-614
-
-
Ribera, E.1
Rodriguez-Pardo, D.2
Rubio, M.3
-
10
-
-
4444297218
-
Safety and efficacy of a simplified fixed-dose combination of stavudine, lamivudine and nevirapine (GPO-VIR) for the treatment of advanced HIV-infected patients: A 24-week study
-
Anekthananon T, Ratanasuwan W, Techasathit W, Sonjai A, Suwanagool S. Safety and efficacy of a simplified fixed-dose combination of stavudine, lamivudine and nevirapine (GPO-VIR) for the treatment of advanced HIV-infected patients: a 24-week study. J Med Assoc Thai 2004; 87: 760-767.
-
(2004)
J Med Assoc Thai
, vol.87
, pp. 760-767
-
-
Anekthananon, T.1
Ratanasuwan, W.2
Techasathit, W.3
Sonjai, A.4
Suwanagool, S.5
-
11
-
-
0034115801
-
The steady-state pharmacokinetics of nevirapine during once daily and twice daily dosing in HIV-1-infected individuals
-
van Heeswijk RP, Veldkamp AI, Mulder JW, et al. The steady-state pharmacokinetics of nevirapine during once daily and twice daily dosing in HIV-1-infected individuals. AIDS 2000; 14: F77-F82.
-
(2000)
AIDS
, vol.14
-
-
van Heeswijk, R.P.1
Veldkamp, A.I.2
Mulder, J.W.3
-
12
-
-
26744433521
-
Preformulation studies of nevirapine, a reverse transcriptase inhibitor
-
Hawi A, Bell G. Preformulation studies of nevirapine, a reverse transcriptase inhibitor. Pharm Res 1994; 11(Suppl): S236.
-
(1994)
Pharm Res
, vol.11
, Issue.SUPPL.
-
-
Hawi, A.1
Bell, G.2
-
13
-
-
0033384441
-
Single dose pharmacokinetics and bioavailability of nevirapine in healthy volunteers
-
Lamson MJ, Sabo JP, MacGregor TR, et al. Single dose pharmacokinetics and bioavailability of nevirapine in healthy volunteers. Biopharm Drug Dispos 1999; 20: 285-291.
-
(1999)
Biopharm Drug Dispos
, vol.20
, pp. 285-291
-
-
Lamson, M.J.1
Sabo, J.P.2
MacGregor, T.R.3
-
14
-
-
71449125747
-
Assessment of nevirapine bioavailability from targeted sites in the human gastrointestinal tract
-
30 September
-
Macha S, Yong C, MacGregor T, et al. Assessment of nevirapine bioavailability from targeted sites in the human gastrointestinal tract. J Clin Pharmacol 2009; published online 30 September 2009.
-
(2009)
J Clin Pharmacol 2009; published online
-
-
Macha, S.1
Yong, C.2
MacGregor, T.3
-
15
-
-
73349092070
-
-
Guidance for Industry. Dissolution Testing of Immediate Release Solid Oral Dosage Forms. FDA, CDER, 1997.
-
Guidance for Industry. Dissolution Testing of Immediate Release Solid Oral Dosage Forms. FDA, CDER, 1997.
-
-
-
-
16
-
-
34548137272
-
Quantitation of five nevirapine oxidative metabolites in human plasma using liquid chromatography-tandem mass spectrometry
-
Rowland LS, MacGregor TR, Campbell SJ, Jenkins R, Pearsall AB, Morris JP. Quantitation of five nevirapine oxidative metabolites in human plasma using liquid chromatography-tandem mass spectrometry. J Chromatogr B 2007; 856: 252-260.
-
(2007)
J Chromatogr B
, vol.856
, pp. 252-260
-
-
Rowland, L.S.1
MacGregor, T.R.2
Campbell, S.J.3
Jenkins, R.4
Pearsall, A.B.5
Morris, J.P.6
-
17
-
-
0342702115
-
Effect of dosage form on drug absorption, a frequent variable in clinical pharmacology
-
Levy G. Effect of dosage form on drug absorption, a frequent variable in clinical pharmacology. Arch Int Pharmacodyn 1964; 52: 59-68.
-
(1964)
Arch Int Pharmacodyn
, vol.52
, pp. 59-68
-
-
Levy, G.1
-
18
-
-
0013792669
-
Dissolution rate limited absorption in man: Factors influencing drug absorption from prolonged-release dosage form
-
Levy G, Hollister LE. Dissolution rate limited absorption in man: factors influencing drug absorption from prolonged-release dosage form. J Pharm Sci 1965; 54: 1121-1125.
-
(1965)
J Pharm Sci
, vol.54
, pp. 1121-1125
-
-
Levy, G.1
Hollister, L.E.2
-
19
-
-
73349108348
-
-
Guidance for Industry. Extended Release Oral Dosage Forms: Development, Evaluation, and Application of In Vitro/In Vivo Correlations. FDA, CDER, 1997.
-
Guidance for Industry. Extended Release Oral Dosage Forms: Development, Evaluation, and Application of In Vitro/In Vivo Correlations. FDA, CDER, 1997.
-
-
-
|