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1
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3843151487
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SOLO: 48-week efficacy and safety comparison of once-daily fosamprenavir/ritonavir versus twice-daily nelfinavir in naive HIV-1-infected patients
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Gathe JC Jr, Ive P, Wood R, et al.: SOLO: 48-week efficacy and safety comparison of once-daily fosamprenavir/ritonavir versus twice-daily nelfinavir in naive HIV-1-infected patients. AIDS 2004;18:1529-1537.
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AIDS
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, pp. 1529-1537
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Gathe Jr, J.C.1
Ive, P.2
Wood, R.3
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2
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33746706779
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The KLEAN study of fosamprenavir-ritonavir versus lopinavir-ritonavir, each in combination with abacavir-lamivudine, for initial treatment of HIV infection over 48 weeks: A randomized non-inferiority trial
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Eron J Jr, Yeni P, Gathe J Jr, et al.: The KLEAN study of fosamprenavir-ritonavir versus lopinavir-ritonavir, each in combination with abacavir-lamivudine, for initial treatment of HIV infection over 48 weeks: A randomized non-inferiority trial. Lancet 2006;368:476-482.
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Lancet
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, pp. 476-482
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Eron Jr, J.1
Yeni, P.2
Gathe Jr, J.3
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3
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64849112459
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The CONTEXT study: Efficacy and safety of GW433908/RTV in PI-experienced subjects with virological failure - 24-week results. Presented at the 10th Conference on Retroviruses and Opportunistic Infections. Boston, MA
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February 10-14
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DeJesus E, Lamarca A, Sension M, et al.: The CONTEXT study: Efficacy and safety of GW433908/RTV in PI-experienced subjects with virological failure - 24-week results. Presented at the 10th Conference on Retroviruses and Opportunistic Infections. Boston, MA, February 10-14, 2003. Abstract/ presentation 178.
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(2003)
Abstract/ presentation 178
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DeJesus, E.1
Lamarca, A.2
Sension, M.3
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5
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33846601305
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Plasma amprenavir pharmacokinetics and tolerability following administration of 1,400 milligrams of fosamprenavir once daily in combination with either 100 or 200 milligrams of ritonavir in healthy volunteers
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Ruane PJ, Luber AD, Wire MB, et al.: Plasma amprenavir pharmacokinetics and tolerability following administration of 1,400 milligrams of fosamprenavir once daily in combination with either 100 or 200 milligrams of ritonavir in healthy volunteers. Antimicrob Agents Chemother 2007;51: 560-565.
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(2007)
Antimicrob Agents Chemother
, vol.51
, pp. 560-565
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Ruane, P.J.1
Luber, A.D.2
Wire, M.B.3
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6
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43149106498
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Fosamprenavir or atazanavir once daily boosted with ritonavir 100 mg, plus tenofovir/ emtricitabine, for the initial treatment of HIV infection: 48-week results of ALERT
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Smith KY, Weinberg WG, DeJesus E, et al.: Fosamprenavir or atazanavir once daily boosted with ritonavir 100 mg, plus tenofovir/ emtricitabine, for the initial treatment of HIV infection: 48-week results of ALERT. AIDS Res Ther 2008; 5(5):1-10.
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(2008)
AIDS Res Ther
, vol.5
, Issue.5
, pp. 1-10
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Smith, K.Y.1
Weinberg, W.G.2
DeJesus, E.3
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7
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43149088419
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Fosamprenavir (FPV) with low-dose ritonavir (RTV) once-daily (QD) in HIV-infected subjects
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Presented at the, Lisbon, Portugal, April 20-22, Abstract/poster
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Hsu R, Walker-Reed K, and Acosta E: Fosamprenavir (FPV) with low-dose ritonavir (RTV) once-daily (QD) in HIV-infected subjects. Presented at the 7th International Workshop on Clinical Pharmacology of HIV Therapy, Lisbon, Portugal, April 20-22, 2006. Abstract/poster 71.
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(2006)
7th International Workshop on Clinical Pharmacology of HIV Therapy
, pp. 71
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Hsu, R.1
Walker-Reed, K.2
Acosta, E.3
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8
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84868920070
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Denver, Colorado, October 14-17, Poster 110E
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+ patients and in antiretroviral-experienced patients switched to FPV/r due to intolerance to prior regimens: BOLD100 (COL109766). Presentedatthe American Collegeof Clinical Pharmacy 2007 Annual Meeting, Denver, Colorado, October 14-17, 2007. Poster 110E.
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(2007)
+ patients and in antiretroviral-experienced patients switched to FPV/r due to intolerance to prior regimens: BOLD100 (COL109766). Presentedatthe American Collegeof Clinical Pharmacy 2007 Annual Meeting
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Blick, G.1
Greiger-Zanlungo, P.2
Plansencia, V.3
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9
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84868925364
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Fosamprenavir boosted with a single 100mg capsule of ritonavir as part of a once daily first line regimen in näive patients
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Presented at the, Glasgow, UK, November 12-16, Poster P17
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DeWit S, Poll B, Necsoi C, and Clumeck N: Fosamprenavir boosted with a single 100mg capsule of ritonavir as part of a once daily first line regimen in näive patients. Presented at the 8th International Congress on Drug Therapy in HIV Infection, Glasgow, UK, November 12-16, 2006. Poster P17.
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(2006)
8th International Congress on Drug Therapy in HIV Infection
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DeWit, S.1
Poll, B.2
Necsoi, C.3
Clumeck, N.4
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10
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84868933265
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Assessment of am-prenavir plasma Cmin levels in patients receiving once-daily fosamprenavir in combination with either 100 or 200mg ritonavir
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Presented at the, Toulouse, France, April, Abstract 216
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Muret P, Muret P, Montange D, et al.: Assessment of am-prenavir plasma Cmin levels in patients receiving once-daily fosamprenavir in combination with either 100 or 200mg ritonavir. Presented at the Congrès P2T Physiology, Pharmacology and Thérapeutics, Toulouse, France, April 2007. Abstract 216.
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(2007)
Congrès P2T Physiology, Pharmacology and Thérapeutics
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Muret, P.1
Muret, P.2
Montange, D.3
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11
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64849116906
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National Institute of Allergy and Infectious Diseases (NIAID, Table for Grading the Severity of Adult and Pediatric Adverse Events, Version 1.0. Division of Acquired Immunodeficiency Syndrome DAIDS, Washington, DC, 2004
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National Institute of Allergy and Infectious Diseases (NIAID): Table for Grading the Severity of Adult and Pediatric Adverse Events, Version 1.0. Division of Acquired Immunodeficiency Syndrome (DAIDS), Washington, DC, 2004.
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12
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64849100279
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Limb and trunk fat changes by total body DEXA alter 96 weeks of treatment with once-daily (QD) fosamprenavir (FPV) boosted with either 100mg or 200mg of ritonavir (/r) plus abacavir (ABC)/lamivudine (3TC): COL100758
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Presented at the, Washington, DC, October 25-28, Abstract
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Wohl D, DeJesus E, Sloan L, et al.: Limb and trunk fat changes by total body DEXA alter 96 weeks of treatment with once-daily (QD) fosamprenavir (FPV) boosted with either 100mg or 200mg of ritonavir (/r) plus abacavir (ABC)/lamivudine (3TC): COL100758. Presented at the 48th Annual ICAAC/IDSA 46th Annual Meeting, Washington, DC, October 25-28, 2008. Abstract.
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(2008)
48th Annual ICAAC/IDSA 46th Annual Meeting
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Wohl, D.1
DeJesus, E.2
Sloan, L.3
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13
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35748933494
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Update of the drug resistance mutations in HIV-1: 2007
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Johnson VA, Brun-Vézinet F, Clotet B, et al.: Update of the drug resistance mutations in HIV-1: 2007. Top HIV Med 2007;15:119-125.
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(2007)
Top HIV Med
, vol.15
, pp. 119-125
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Johnson, V.A.1
Brun-Vézinet, F.2
Clotet, B.3
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14
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0033574249
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A more accurate method to estimate glomerular filtration rate from serum creatinine: A new prediction equation
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for the Modification of Diet in Renal Disease Study Group
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Levey AS, Bosch JP, Lewis JB, et al., for the Modification of Diet in Renal Disease Study Group: A more accurate method to estimate glomerular filtration rate from serum creatinine: A new prediction equation. Ann Intern Med 1999;130:461-470.
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(1999)
Ann Intern Med
, vol.130
, pp. 461-470
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Levey, A.S.1
Bosch, J.P.2
Lewis, J.B.3
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15
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1642283134
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GW433908/ritonavir once daily in antiretroviral therapy-naïve HIV-infected patients: Absence of protease resistance at 48 weeks
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MacManus, Yates PJ, Elston RC, et al.: GW433908/ritonavir once daily in antiretroviral therapy-naïve HIV-infected patients: Absence of protease resistance at 48 weeks. AIDS 2004; 18:651-655.
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(2004)
AIDS
, vol.18
, pp. 651-655
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MacManus1
Yates, P.J.2
Elston, R.C.3
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16
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0038360368
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GW433908 in ART-naïve subjects: Absence of resistance at 48 weeks with boosted regimen and APV-like resistance profile with unboosted regimen
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Presented at the, Boston, MA, February 10-14, Abstract/poster
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MacManus S, Yates PJ, White S, Richards N, and Snowden W: GW433908 in ART-naïve subjects: Absence of resistance at 48 weeks with boosted regimen and APV-like resistance profile with unboosted regimen. Presented at the 10th Conference on Retroviruses and Opportunistic Infections, Boston, MA, February 10-14, 2003. Abstract/poster 598.
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(2003)
10th Conference on Retroviruses and Opportunistic Infections
, pp. 598
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MacManus, S.1
Yates, P.J.2
White, S.3
Richards, N.4
Snowden, W.5
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17
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0036173443
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Pharmacokinetic modeling and simulations of interaction of amprenavir and ritonavir
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Sale M, Sadler BM, and Stein DS: Pharmacokinetic modeling and simulations of interaction of amprenavir and ritonavir. Antimicrob Agents Chemother 2002;46:746-754.
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(2002)
Antimicrob Agents Chemother
, vol.46
, pp. 746-754
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Sale, M.1
Sadler, B.M.2
Stein, D.S.3
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18
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9144240623
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Six-week randomized controlled trial to compare the tolerabilities, pharmaco-kinetics, and antiviral activities of GW433908 and amprenavir in human immunodeficiency virus type 1-infected patients
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Wood R, Arasteh K, Stellbring H-J, et al.: Six-week randomized controlled trial to compare the tolerabilities, pharmaco-kinetics, and antiviral activities of GW433908 and amprenavir in human immunodeficiency virus type 1-infected patients. Antimicrob Agents Chemother 2004;48:116-123.
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(2004)
Antimicrob Agents Chemother
, vol.48
, pp. 116-123
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Wood, R.1
Arasteh, K.2
Stellbring, H.-J.3
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19
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84868928222
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+ patients stabilized on fosamprenavir (FPV) 1400mg+FTC/TDF 200/ 300mg QD boosted by RTV 100mg QD (TELEX II)
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Presented at the, Budapest, Hungary, April 16-18, Abstract/poster
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+ patients stabilized on fosamprenavir (FPV) 1400mg+FTC/TDF 200/ 300mg QD boosted by RTV 100mg QD (TELEX II). Presented at the 8th International Workshop on Clinical Pharmacology of HIV Therapy, Budapest, Hungary, April 16-18, 2007. Abstract/poster 22.
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(2007)
8th International Workshop on Clinical Pharmacology of HIV Therapy
, pp. 22
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Parks, D.1
Jennings, H.2
Taylor, C.3
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