-
1
-
-
2642709177
-
Declining morbidity and mortality among patients with advanced human immunodeficiency virus infection
-
Palella F, Delaney K, Moorman A, et al. Declining morbidity and mortality among patients with advanced human immunodeficiency virus infection. N Engl J Med 1998:338:853-60.
-
(1998)
N. Engl. J. Med.
, vol.338
, pp. 853-860
-
-
Palella, F.1
Delaney, K.2
Moorman, A.3
-
2
-
-
0037055025
-
Antiretroviral treatment for adult HIV infection in 2002: Updated recommendations of the International AIDS Society-USA Panel
-
Yeni P, Hammer S, Carpenter C, et al. Antiretroviral treatment for adult HIV infection in 2002: updated recommendations of the International AIDS Society-USA Panel. JAMA 2002:288:222-35.
-
(2002)
JAMA
, vol.288
, pp. 222-235
-
-
Yeni, P.1
Hammer, S.2
Carpenter, C.3
-
3
-
-
0037192582
-
Improved long-term suppression of HIV-1 replication with a triple-class multidrug regimen compared with standard of care antiretroviral therapy
-
Van Praag R, Wit F, Jurriaans S, De Wolf F, Prins J, Lange J. Improved long-term suppression of HIV-1 replication with a triple-class multidrug regimen compared with standard of care antiretroviral therapy. AIDS 2002;16:719-25.
-
(2002)
AIDS
, vol.16
, pp. 719-725
-
-
Van Praag, R.1
Wit, F.2
Jurriaans, S.3
De Wolf, F.4
Prins, J.5
Lange, J.6
-
5
-
-
0035117801
-
Use of HIV protease inhibitors as pharmacoenhancers
-
Moyle G. Use of HIV protease inhibitors as pharmacoenhancers. AIDS Read 2001;11:87-98.
-
(2001)
AIDS Read
, vol.11
, pp. 87-98
-
-
Moyle, G.1
-
6
-
-
0037339136
-
The role of pharmacological enhancement in protease inhibitor-based highly active antiretroviral therapy
-
Becker S. The role of pharmacological enhancement in protease inhibitor-based highly active antiretroviral therapy. Expert Opin Investig Drugs 2003:12:401-12.
-
(2003)
Expert. Opin. Investig. Drugs
, vol.12
, pp. 401-412
-
-
Becker, S.1
-
7
-
-
0034455640
-
Using pharmacokinetics to optimize antiretroviral drug-drug interactions in the treatment of human immunodeficiency virus infection
-
Gerber J. Using pharmacokinetics to optimize antiretroviral drug-drug interactions in the treatment of human immunodeficiency virus infection. Clin Infect Dis 2000;30 Suppl 2:123-9.
-
(2000)
Clin. Infect. Dis.
, vol.30
, Issue.SUPPL. 2
, pp. 123-129
-
-
Gerber, J.1
-
9
-
-
0032971472
-
Ritonavir and saquinavir combination therapy for the treatment of HIV infection
-
Cameron D, Japour A, Xu Y, et al. Ritonavir and saquinavir combination therapy for the treatment of HIV infection. AIDS 1999;13:213-24.
-
(1999)
AIDS
, vol.13
, pp. 213-224
-
-
Cameron, D.1
Japour, A.2
Xu, Y.3
-
10
-
-
0042945648
-
Steady-state pharmacokinetic interaction study between BMS-232632 and ritonavir in healthy subjects
-
8th CROI; February Chicago (IL) [abstract 740]
-
O'Mara E, Mummaneni V, Bifano M, et al. Steady-state pharmacokinetic interaction study between BMS-232632 and ritonavir in healthy subjects. 8th CROI; February 2001; Chicago (IL) [abstract 740].
-
(2001)
-
-
O'Mara, E.1
Mummaneni, V.2
Bifano, M.3
-
11
-
-
0041944069
-
Steady-state pharmacokinetic (PK) interaction study of atazanavir (ATV) with ritonavir (RTV) in healthy subjects
-
42nd ICAAC; September San Diego (CA). Abstract Book. Herndon, VA: ASM Press; [abstract H-1716]
-
Agarwala S, Russo R, Mummaneni V, Randall D, Geraldes M, O'Mara E. Steady-state pharmacokinetic (PK) interaction study of atazanavir (ATV) with ritonavir (RTV) in healthy subjects. 42nd ICAAC; September 2002; San Diego (CA). Abstract Book. Herndon, VA: ASM Press; 274 [abstract H-1716].
-
(2002)
, pp. 274
-
-
Agarwala, S.1
Russo, R.2
Mummaneni, V.3
Randall, D.4
Geraldes, M.5
O'Mara, E.6
-
12
-
-
13644265237
-
-
Bristol-Myers Squibb Company. BMS-232632: Atazanavir Briefing Document May, 2003. Accessed March 22
-
Bristol-Myers Squibb Company. BMS-232632: Atazanavir Briefing Document May, 2003. http://www.fda.gov/ohrms/dockets/ac/03/briefing/ 3950B1_01_bristolmyerssquibb-atazanavir.pdf. Accessed March 22, 2004.
-
(2004)
-
-
-
13
-
-
0036694265
-
Low-dose ritonavir moderately enhances nelfinavir exposure
-
Kurowski M, Kaeser B, Sawyer A, Popescu M, Mrozikiewicz A. Low-dose ritonavir moderately enhances nelfinavir exposure. Clin Pharmacol Ther 2002;72:123-32.
-
(2002)
Clin. Pharmacol. Ther.
, vol.72
, pp. 123-132
-
-
Kurowski, M.1
Kaeser, B.2
Sawyer, A.3
Popescu, M.4
Mrozikiewicz, A.5
-
14
-
-
0034027217
-
Adherence to protease inhibitors, HIV-1 viral load, and development of drug resistance in an indigent population
-
Bangsberg D, Hecht F, Charlebois E, et al. Adherence to protease inhibitors, HIV-1 viral load, and development of drug resistance in an indigent population. AIDS 2000;14:357-66.
-
(2000)
AIDS
, vol.14
, pp. 357-366
-
-
Bangsberg, D.1
Hecht, F.2
Charlebois, E.3
-
15
-
-
0142218458
-
Association between adherence to antiretroviral therapy and human immunodeficiency virus drug resistance
-
Sethi A, Celentano D, Gange S, Moore R, Gallant J. Association between adherence to antiretroviral therapy and human immunodeficiency virus drug resistance. Clin Infect Dis 2003;37:1112-8.
-
(2003)
Clin. Infect. Dis.
, vol.37
, pp. 1112-1118
-
-
Sethi, A.1
Celentano, D.2
Gange, S.3
Moore, R.4
Gallant, J.5
-
16
-
-
0036895440
-
Virtual inhibitory quotient predicts response to ritonavir boosting of indinavir-based therapy in human immunodeficiency virus-infected patients with ongoing viremia
-
Shulman N, Zolopa A, Havlir D, et al. Virtual inhibitory quotient predicts response to ritonavir boosting of indinavir-based therapy in human immunodeficiency virus-infected patients with ongoing viremia. Antimicrob Agents Chemother 2002;46:3907-16.
-
(2002)
Antimicrob. Agents Chemother.
, vol.46
, pp. 3907-3916
-
-
Shulman, N.1
Zolopa, A.2
Havlir, D.3
-
17
-
-
0037308542
-
Genotypic inhibitory quotient as predictor of virological response to ritonavir-amprenavir in human immunodeficiency virus type 1 protease inhibitor-experienced patients
-
and the Genophar Study Group
-
Marcelin A, Lamotte C, Delaugerre C, et al., and the Genophar Study Group. Genotypic inhibitory quotient as predictor of virological response to ritonavir-amprenavir in human immunodeficiency virus type 1 protease inhibitor-experienced patients. Antimicrob Agents Chemother 2003;47:594-600.
-
(2003)
Antimicrob. Agents Chemother.
, vol.47
, pp. 594-600
-
-
Marcelin, A.1
Lamotte, C.2
Delaugerre, C.3
-
18
-
-
1642389500
-
Characterization of the impact of genotype, phenotype, and inhibitory quotient on antiviral activity of tipranavir in highly treatment-experienced patients
-
[abstract 12]
-
McCallister S, Kohlbrenner V, Squires K, et al. Characterization of the impact of genotype, phenotype, and inhibitory quotient on antiviral activity of tipranavir in highly treatment-experienced patients. Antivir Ther 2003;8 Suppl 1:15[abstract 12].
-
(2003)
Antivir. Ther.
, vol.8
, Issue.SUPPL. 1
, pp. 15
-
-
McCallister, S.1
Kohlbrenner, V.2
Squires, K.3
-
19
-
-
9144271024
-
Incidence of resistance in a double-blind study comparing lopinavir/ritonavir plus stavudine and lamivudine to nelfinavir plus stavudine and lamivudine
-
Kempf D, King M, Bernstein B, et al. Incidence of resistance in a double-blind study comparing lopinavir/ritonavir plus stavudine and lamivudine to nelfinavir plus stavudine and lamivudine. J Infect Dis 2004;189:51-60.
-
(2004)
J. Infect. Dis.
, vol.189
, pp. 51-60
-
-
Kempf, D.1
King, M.2
Bernstein, B.3
-
20
-
-
0038360368
-
GW433908 in ART-naive subjects: Absence of resistance at 48 weeks with boosted regimen and APV-like resistance profile with unboosted regimen
-
10th CROI; February Boston (MA) [abstract 598]
-
Macmanus S, Yates P, White S, Richards N, Snowden W. GW433908 in ART-naive subjects: absence of resistance at 48 weeks with boosted regimen and APV-like resistance profile with unboosted regimen. 10th CROI; February 2003; Boston (MA) [abstract 598].
-
(2003)
-
-
Macmanus, S.1
Yates, P.2
White, S.3
Richards, N.4
Snowden, W.5
-
21
-
-
0034906186
-
Disorders of lipid metabolism in patients with HIV disease treated with antiretroviral agents: Frequency, relationship with administered drugs, and role of hypolipidemic therapy with bezafibrate
-
Manfredi R, Chiodo F. Disorders of lipid metabolism in patients with HIV disease treated with antiretroviral agents: frequency, relationship with administered drugs, and role of hypolipidemic therapy with bezafibrate. J Infect 2001;42:181-8.
-
(2001)
J. Infect.
, vol.42
, pp. 181-188
-
-
Manfredi, R.1
Chiodo, F.2
-
22
-
-
0033873920
-
Hyperlipidemia associated with HIV protease inhibitor use: Pathophysiology, prevalence, risk factors and treatment
-
Penzak S, Chuck S. Hyperlipidemia associated with HIV protease inhibitor use: pathophysiology, prevalence, risk factors and treatment. Scand J Infect Dis 2000;32:111-23.
-
(2000)
Scand. J. Infect. Dis.
, vol.32
, pp. 111-123
-
-
Penzak, S.1
Chuck, S.2
-
23
-
-
0035461510
-
Saquinavir and ritonavir pharmacokinetics following combined ritonavir and saquinavir (soft gelatin capsules) administration
-
Buss N, Snell P, Bock J, Hsu A, Jorge K. Saquinavir and ritonavir pharmacokinetics following combined ritonavir and saquinavir (soft gelatin capsules) administration. Br J Clin Pharmacol 2001; 52:255-64.
-
(2001)
Br. J. Clin. Pharmacol.
, vol.52
, pp. 255-264
-
-
Buss, N.1
Snell, P.2
Bock, J.3
Hsu, A.4
Jorge, K.5
-
24
-
-
0013309175
-
Continued indinavir vs. switching to indinavir/ritonavir in HIV-infected patients with suppressed viral load
-
for the BEST Study Team
-
Arnaiz J, Mallolas J, Podzamczer D, et al., for the BEST Study Team. Continued indinavir vs. switching to indinavir/ritonavir in HIV-infected patients with suppressed viral load. AIDS 2003;17:831-40.
-
(2003)
AIDS
, vol.17
, pp. 831-840
-
-
Arnaiz, J.1
Mallolas, J.2
Podzamczer, D.3
-
25
-
-
17044457456
-
Lopinavir plasma concentrations and changes in lipid levels during salvage therapy with lopinavir/ritonavir-containing regimens
-
Gutiérrez F, Padilla S, Navarro A, et al. Lopinavir plasma concentrations and changes in lipid levels during salvage therapy with lopinavir/ritonavir-containing regimens. J Acquir Immune Defic Syndr 2003;33:594-600.
-
(2003)
J. Acquir. Immune Defic. Syndr.
, vol.33
, pp. 594-600
-
-
Gutiérrez, F.1
Padilla, S.2
Navarro, A.3
-
26
-
-
0006843725
-
A randomized study comparing continued indinavir (800 mg tid) vs. switching to indinavir/ritonavir (800/100 mg bid) in HIV patients having achieved viral load suppression with indinavir plus 2 nucleoside analogues
-
The Bid Efficacy and Safety Trial (BEST). XIII International AIDS Conference Barcelona [abstract WeOrB484]
-
Gatell J, Lange J, Arnaiz J, Faetkenheuer G, Mallolas J, Clotet B. A randomized study comparing continued indinavir (800 mg tid) vs. switching to indinavir/ritonavir (800/100 mg bid) in HIV patients having achieved viral load suppression with indinavir plus 2 nucleoside analogues. The Bid Efficacy and Safety Trial (BEST). XIII International AIDS Conference; 2000; Barcelona [abstract WeOrB484].
-
(2000)
-
-
Gatell, J.1
Lange, J.2
Arnaiz, J.3
Faetkenheuer, G.4
Mallolas, J.5
Clotet, B.6
-
27
-
-
0036499067
-
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 inhibitor-experienced patients
-
Benson C, Deeks S, Brun S, 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 inhibitor-experienced patients. J Infect Dis 2002;185:599-607.
-
(2002)
J. Infect. Dis.
, vol.185
, pp. 599-607
-
-
Benson, C.1
Deeks, S.2
Brun, S.3
-
28
-
-
0002472332
-
Durable suppression of HIV+ RNA after 2 years of therapy with ABT-378/ritonavir (ABT-378/r) treatment in single protease inhibitor experienced patients
-
for the M97-765 Study Group. [abstract P101]
-
Feinberg J, Brun S, Xu Y, et al., for the M97-765 Study Group. Durable suppression of HIV+ RNA after 2 years of therapy with ABT-378/ritonavir (ABT-378/r) treatment in single protease inhibitor experienced patients. AIDS 2000;14 Suppl 4:46[abstract P101].
-
(2000)
AIDS
, vol.14
, Issue.SUPPL. 4
, pp. 46
-
-
Feinberg, J.1
Brun, S.2
Xu, Y.3
-
29
-
-
0005678653
-
Kaletra (lopinavir/ritonavir) and efavirenz: 72 week safety/efficacy evaluation and phenotypic/genotypic breakpoints in multiple PI experienced patients
-
41st ICAAC; December Chicago (IL) [abstract 344]. [abstract I-1925]
-
Danner S, Brun S, Sylte J, et al. Kaletra (lopinavir/ritonavir) and efavirenz: 72 week safety/efficacy evaluation and phenotypic/genotypic breakpoints in multiple PI experienced patients [abstract I-1925]. 41st ICAAC; December 2001; Chicago (IL) [abstract 344].
-
(2001)
-
-
Danner, S.1
Brun, S.2
Sylte, J.3
-
30
-
-
0035986072
-
Salvage treatment with lopinavir/ritonavir (Kaletra) in HIV-infected patients failing all current antiretroviral drug families
-
De Mendoza C, Martín-Carbonero L, Barreiro P, et al. Salvage treatment with lopinavir/ritonavir (Kaletra) in HIV-infected patients failing all current antiretroviral drug families. HIV Clin Trials 2002;3:304-9.
-
(2002)
HIV Clin. Trials
, vol.3
, pp. 304-309
-
-
De Mendoza, C.1
Martín-Carbonero, L.2
Barreiro, P.3
-
31
-
-
0037114877
-
Open-label study of a twice-daily indinavir 800 mg/ritonavir 200 mg regimen in HIV-infected adults failing a protease inhibitor regimen
-
Katner H, Paar D, Nadler J, et al. Open-label study of a twice-daily indinavir 800 mg/ritonavir 200 mg regimen in HIV-infected adults failing a protease inhibitor regimen. J Acquir Immune Defic Syndr 2002;31:483-7.
-
(2002)
J. Acquir. Immune Defic. Syndr.
, vol.31
, pp. 483-487
-
-
Katner, H.1
Paar, D.2
Nadler, J.3
-
32
-
-
13644262930
-
Indinavir tid vs. indinavir/ritonavir bid in combination with AZT/3TC for HIV infection in nucleoside pretreated patients: HIV-NAT 005 76-week follow up
-
9th CROI; February Seattle (WA) [poster 422-W]
-
Boyd M, Duncombe C, Ruxrungthram K, et al. Indinavir tid vs. indinavir/ritonavir bid in combination with AZT/3TC for HIV infection in nucleoside pretreated patients: HIV-NAT 005 76-week follow up. 9th CROI; February 2002; Seattle (WA) [poster 422-W].
-
(2002)
-
-
Boyd, M.1
Duncombe, C.2
Ruxrungthram, K.3
-
33
-
-
27344437653
-
Final analysis of a randomized trial to evaluate safety and efficacy of indinavir/ritonavir versus saquinavir/ritonavir in adult HIV-1 infection: The MaxCmin1 Trial
-
42nd ICAAC; September San Diego (CA) [abstract H-172]
-
Gerstoft J, Dragsted U, Cahn P, et al. Final analysis of a randomized trial to evaluate safety and efficacy of indinavir/ritonavir versus saquinavir/ritonavir in adult HIV-1 infection: the MaxCmin1 Trial. 42nd ICAAC; September 2002; San Diego (CA) [abstract H-172].
-
(2002)
-
-
Gerstoft, J.1
Dragsted, U.2
Cahn, P.3
-
34
-
-
0038575809
-
Saquinavir: A review of its use in boosted regimens for treating HIV infection
-
Plosker G, Scott L. Saquinavir: a review of its use in boosted regimens for treating HIV infection. Drugs 2003;63:1299-324.
-
(2003)
Drugs
, vol.63
, pp. 1299-1324
-
-
Plosker, G.1
Scott, L.2
-
35
-
-
0141612910
-
Randomized trial to evaluate indinavir/ritonavir vs. saquinavir/ritonavir in human immunodeficiency virus type 1-infected patients: The MaxCmin1 Trial
-
for the MaxCmin1 Trial Group
-
Dragsted U, Gerstoft J, Pedersen C, et al., for the MaxCmin1 Trial Group. Randomized trial to evaluate indinavir/ritonavir vs. saquinavir/ritonavir in human immunodeficiency virus type 1-infected patients: the MaxCmin1 Trial. J Infect Dis 2003;188:635-42.
-
(2003)
J. Infect. Dis.
, vol.188
, pp. 635-642
-
-
Dragsted, U.1
Gerstoft, J.2
Pedersen, C.3
-
36
-
-
22844439930
-
The final week 48 analysis of a phase IV, randomised, open-label, multi-centre trial to evaluate safety and efficacy of lopinavir/ritonavir (400/100 mg bid) vs. saquinavir/ritonavir (1000/100 mg bid) in adult HIV-1 infection: The MaxCmin2 Trial
-
2nd International AIDS Society Conference on HIV Pathogenesis and Treatment; July Paris [poster LB23]
-
Youle M, Gerstoft J, Fox Z, et al. The final week 48 analysis of a phase IV, randomised, open-label, multi-centre trial to evaluate safety and efficacy of lopinavir/ritonavir (400/100 mg bid) vs. saquinavir/ritonavir (1000/100 mg bid) in adult HIV-1 infection: the MaxCmin2 Trial. 2nd International AIDS Society Conference on HIV Pathogenesis and Treatment; July 2003; Paris [poster LB23].
-
(2003)
-
-
Youle, M.1
Gerstoft, J.2
Fox, Z.3
-
37
-
-
22844439930
-
The final week 48 analysis of a phase IV, randomised, open-label, multi-center trial to evaluate safety and efficacy of lopinavir/ritonavir (400/100 mg bid) vs. saquinavir/ritonavir (1000/100 mg bid): The MaxCMin2 Trial
-
9th European AIDS Conference (EACS); October Warsaw [abstract F11/3]
-
Youle M, Gerstoft J, Fox Z, et al. The final week 48 analysis of a phase IV, randomised, open-label, multi-center trial to evaluate safety and efficacy of lopinavir/ritonavir (400/100 mg bid) vs. saquinavir/ritonavir (1000/100 mg bid): The MaxCMin2 Trial. 9th European AIDS Conference (EACS); October 2003; Warsaw [abstract F11/3].
-
(2003)
-
-
Youle, M.1
Gerstoft, J.2
Fox, Z.3
-
38
-
-
13644258146
-
Lipid profiles of patients enrolled in the MaxCmin 2 trial: A randomized, open-label multicenter comparative trial evaluating the safety and efficacy of lopinavir/ritonavir (400/100 mg twice daily) vs. saquinavir/ritonavir SQV/r (1000/100 mg twice daily)
-
11th CROI; February San Francisco (CA) [abstract 720]
-
Walmsley S, Benetucci J, Brutus A, et al. Lipid profiles of patients enrolled in the MaxCmin 2 trial: a randomized, open-label multicenter comparative trial evaluating the safety and efficacy of lopinavir/ritonavir (400/100 mg twice daily) vs. saquinavir/ritonavir SQV/r (1000/100 mg twice daily). 11th CROI; February 2004, San Francisco (CA) [abstract 720].
-
(2004)
-
-
Walmsley, S.1
Benetucci, J.2
Brutus, A.3
-
39
-
-
2442681710
-
Twice-daily amprenavir 1200 mg vs. amprenavir 600 mg/ ritonavir 100 mg, in combination with at least 2 other antiretroviral drugs, in HIV-1-infected patients
-
and the ESS40011 (STARR) Study Team
-
Nadler J, Gathe J, Pollard R, et al., and the ESS40011 (STARR) Study Team. Twice-daily amprenavir 1200 mg vs. amprenavir 600 mg/ ritonavir 100 mg, in combination with at least 2 other antiretroviral drugs, in HIV-1-infected patients. BMC Infect Dis 2003;3:10.
-
(2003)
BMC Infect. Dis.
, vol.3
, pp. 10
-
-
Nadler, J.1
Gathe, J.2
Pollard, R.3
-
40
-
-
13644256506
-
Efficacy, safety and amprenavir (APV) pharmacokinetic (PK) responses of twice-daily APV and ritonavir (RTV) regimens in HIV-1 infected treatment-experienced adults for 48 weeks (ESS40006)
-
41st ICAAC; September Chicago (IL) [abstract 344]
-
Schooley R, Haubrich R, Sension M, et al. Efficacy, safety and amprenavir (APV) pharmacokinetic (PK) responses of twice-daily APV and ritonavir (RTV) regimens in HIV-1 infected treatment-experienced adults for 48 weeks (ESS40006). 41st ICAAC; September 2001; Chicago (IL) [abstract 344].
-
(2001)
-
-
Schooley, R.1
Haubrich, R.2
Sension, M.3
-
41
-
-
0003351767
-
Amprenavir (APV) 600 mg/ritonavir (RTV) 100 mg bid or APV 1200 mg/RTV 200 mg qd given in combination with abacavir (ABC) and lamivudine (3TC) maintains efficacy in ART naive HIV-1 infected adults over 12 weeks (APV20001)
-
8th CROI; February Chicago (IL) [abstract 332]
-
Wood R, Trepo C, Livrozet J, et al. Amprenavir (APV) 600 mg/ritonavir (RTV) 100 mg bid or APV 1200 mg/RTV 200 mg qd given in combination with abacavir (ABC) and lamivudine (3TC) maintains efficacy in ART naive HIV-1 infected adults over 12 weeks (APV20001). 8th CROI; February 2001; Chicago (IL) [abstract 332].
-
(2001)
-
-
Wood, R.1
Trepo, C.2
Livrozet, J.3
-
42
-
-
0008644635
-
Amprenavir (APV) 600 mg/ritonavir (RTV) 100 mg bid or APV 1.200 mg/RTV 200 mg qd given in combination with abacavir (ABC) and lamivudine (3TC) maintains efficacy in ART naive HIV-1 infected adults over 24-weeks (APV20001)
-
8th European Conference on Clinical Aspects and Treatment of HIV Infection; October Athens [abstract P218]
-
Arasteh K, Wood R, Teofilo E, et al. Amprenavir (APV) 600 mg/ritonavir (RTV) 100 mg bid or APV 1.200 mg/RTV 200 mg qd given in combination with abacavir (ABC) and lamivudine (3TC) maintains efficacy in ART naive HIV-1 infected adults over 24-weeks (APV20001). 8th European Conference on Clinical Aspects and Treatment of HIV infection; October 2001; Athens [abstract P218].
-
(2001)
-
-
Arasteh, K.1
Wood, R.2
Teofilo, E.3
-
43
-
-
0037684348
-
The Context study: Efficacy and safety of GW433908/RTV in PI-experienced subjects with virological failure (24 week results)
-
10th CROI; February Boston (MA) [abstract 178]
-
DeJesus E, LaMarca A, Sension M, Beltrán C, Yeni P. The Context study: efficacy and safety of GW433908/RTV in PI-experienced subjects with virological failure (24 week results). 10th CROI; February 2003; Boston (MA) [abstract 178].
-
(2003)
-
-
DeJesus, E.1
LaMarca, A.2
Sension, M.3
Beltrán, C.4
Yeni, P.5
-
44
-
-
1642370571
-
Vertex reports preliminary 48-week data from phase III study of 433908, an investigational HIV protease inhibitor
-
Vertex Pharmaceuticals Incorporated. Press release. Press release dated July 24, 2003. Available at: www.vpharm.com/Pressreleases2003/pr072403.html. Accessed June 4
-
Vertex Pharmaceuticals Incorporated. Vertex reports preliminary 48-week data from phase III study of 433908, an investigational HIV protease inhibitor. Press release. Press release dated July 24, 2003. Available at: www.vpharm.com/Pressreleases2003/pr072403.html. Accessed June 4, 2004.
-
(2004)
-
-
-
45
-
-
3142662261
-
Efficacy and safety of atazanavir with ritonavir or saquinavir vs. lopinavir/ritonavir in patients who have experienced virologic failure on multiple HAART regimens: 48-week results from BMS A1424-045
-
11th CROI; February San Francisco (CA) [abstract 547]
-
DeJesus E, Grinsztejn B, Rodríguez C, et al. Efficacy and safety of atazanavir with ritonavir or saquinavir vs. lopinavir/ritonavir in patients who have experienced virologic failure on multiple HAART regimens: 48-week results from BMS A1424-045. 11th CROI; February 2004; San Francisco (CA) [abstract 547].
-
(2004)
-
-
DeJesus, E.1
Grinsztejn, B.2
Rodríguez, C.3
-
46
-
-
13644269030
-
Safety assessment of patients receiving atazanavir (9ATV) with ritonavir (RTV), ATV with saquinavir (SQV), or lopinavir (LPV)/RTV: 48-week results from BMS A1424-045
-
13th International Symposium on HIV & Emerging Infectious Diseases; June Toulon, France [abstract PP 4.57]
-
Clotet B, Lazzarin A, Grinsztejn B, Lichtenstein K, Sankoh S, Wilber R. Safety assessment of patients receiving atazanavir (9ATV) with ritonavir (RTV), ATV with saquinavir (SQV), or lopinavir (LPV)/RTV: 48-week results from BMS A1424-045. 13th International Symposium on HIV & Emerging Infectious Diseases; June 2004, Toulon, France [abstract PP 4.57].
-
(2004)
-
-
Clotet, B.1
Lazzarin, A.2
Grinsztejn, B.3
Lichtenstein, K.4
Sankoh, S.5
Wilber, R.6
-
47
-
-
0037234238
-
Results of a phase 2 clinical trial at 48 weeks (AI424-007): A dose-ranging, safety, and efficacy comparative trial of atazanavir at three doses in combination with didanosine and stavudine in antiretroviral-naive subjects
-
for the AI424-007 Clinical Trial Group
-
Sanne I, Piliero P, Squires K, Thiry A, Schnittman S, for the AI424-007 Clinical Trial Group. Results of a phase 2 clinical trial at 48 weeks (AI424-007): a dose-ranging, safety, and efficacy comparative trial of atazanavir at three doses in combination with didanosine and stavudine in antiretroviral-naive subjects. J Acquir Immune Defic Syndr 2003;32:18-29.
-
(2003)
J. Acquir. Immune Defic. Syndr.
, vol.32
, pp. 18-29
-
-
Sanne, I.1
Piliero, P.2
Squires, K.3
Thiry, A.4
Schnittman, S.5
-
48
-
-
0037661234
-
Therapy with atazanavir plus saquinavir in patients failing highly active antiretroviral therapy: A randomized comparative pilot trial
-
Haas D, Zala C, Schrader S, et al. Therapy with atazanavir plus saquinavir in patients failing highly active antiretroviral therapy: a randomized comparative pilot trial. AIDS 2003;17:1339-49.
-
(2003)
AIDS
, vol.17
, pp. 1339-1349
-
-
Haas, D.1
Zala, C.2
Schrader, S.3
-
49
-
-
1642465026
-
Dose-ranging, randomized, clinical trial of atazanavir with lamivudine and stavudine in antiretroviral-naive subjects: 48-week results
-
Murphy R, Sanne I, Cahn P, et al. Dose-ranging, randomized, clinical trial of atazanavir with lamivudine and stavudine in antiretroviral-naive subjects: 48-week results. AIDS 2003;17:2603-14.
-
(2003)
AIDS
, vol.17
, pp. 2603-2614
-
-
Murphy, R.1
Sanne, I.2
Cahn, P.3
-
50
-
-
13644258142
-
The LOPSAQ study: 24-week analysis of the double protease inhibitor (PI) salvage regimen containing lopinavir (LPV/r) plus saquinavir (SQV) without any additional antiretroviral (ART) therapy
-
[abstract 583]
-
Staszewski S, Dauer B, Von Hentig N, et al. The LOPSAQ study: 24-week analysis of the double protease inhibitor (PI) salvage regimen containing lopinavir (LPV/r) plus saquinavir (SQV) without any additional antiretroviral (ART) therapy. Antivir Ther 2003;8 Suppl 1 :342[abstract 583].
-
(2003)
Antivir. Ther.
, vol.8
, Issue.SUPPL. 1
, pp. 342
-
-
Staszewski, S.1
Dauer, B.2
Von Hentig, N.3
-
51
-
-
13644257341
-
Salvage therapy with lopinavir/ritonavir (LPV/R), amprenavir (APV) ± an additional boost with ritonavir (RTV): 1-year results of puzzle 1-ANRS104 study
-
and the Puzzle 1 Group. [abstract 585]
-
Raguin G, Chene G, Morand-Joubert L, and the Puzzle 1 Group. Salvage therapy with lopinavir/ritonavir (LPV/R), amprenavir (APV) ± an additional boost with ritonavir (RTV): 1-year results of puzzle 1-ANRS104 study. Antivir Ther 2003;8 Suppl 1:343[abstract 585].
-
(2003)
Antivir. Ther.
, vol.8
, Issue.SUPPL. 1
, pp. 343
-
-
Raguin, G.1
Chene, G.2
Morand-Joubert, L.3
-
52
-
-
13644258749
-
A pilot study of saquinavir-SGC (SQV) and lopinavir/ritonavir (LPV/R) twice daily in protease inhibitor (PI) naive HIV+ individuals: Protease inhibitor concentrations and week 24 results
-
[abstract 571]
-
Hellinger J, Cohen C, Morris A, et al. A pilot study of saquinavir-SGC (SQV) and lopinavir/ritonavir (LPV/R) twice daily in protease inhibitor (PI) naive HIV+ individuals: protease inhibitor concentrations and week 24 results. Antivir Ther 2003;8 Suppl 1:339[abstract 571].
-
(2003)
Antivir. Ther.
, vol.8
, Issue.SUPPL. 1
, pp. 339
-
-
Hellinger, J.1
Cohen, C.2
Morris, A.3
|