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Fichtenbaum CJ, Gerber JG, Rosenkranz SL. Pharmacokinetic interactions between protease inhibitors and statins in HIV seronegative volunteers: ACTG Study A5047. AIDS 16, 569-577 (2002).
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Fichtenbaum, C.J.1
Gerber, J.G.2
Rosenkranz, S.L.3
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53
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85039513079
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Long-term efficacy and safety of protease inhibitor switching to nevirapine in HIV patients with undetectable viral load
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2nd IAS (Abstract no. 590)
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Gil P, Gorgolas M, Estrada V et al. Long-term efficacy and safety of protease inhibitor switching to nevirapine in HIV patients with undetectable viral load. 2nd IAS (Abstract no. 590).
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Gil, P.1
Gorgolas, M.2
Estrada, V.3
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54
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85039515180
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Efficacy and safety of a once daily regimen with NNRTIs after a successful protease inhibitor-containing regimen
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2nd IAS (Abstract no. 591)
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Moya J, Casado S, Diz A et al. Efficacy and safety of a once daily regimen with NNRTIs after a successful protease inhibitor-containing regimen. 2nd IAS (Abstract no. 591).
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Moya, J.1
Casado, S.2
Diz, A.3
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55
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85039542226
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Preliminary results of ESPRIT (Evaluation of Subcutaneous Proleukin in a Randomised International Trial): Baseline predictors of CD4 T-cell response to interteukin-2
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2nd IAS (Abstract no. 13)
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Weiss L, Aboulhab J, Babiker GA et al. Preliminary results of ESPRIT (Evaluation of Subcutaneous Proleukin in a Randomised International Trial): Baseline predictors of CD4 T-cell response to interteukin-2. 2nd IAS (Abstract no. 13).
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Weiss, L.1
Aboulhab, J.2
Babiker, G.A.3
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56
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85039517949
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Maxcmin 1 compared SQV/r withIDV/r and found that SQV/r was better tolerated the IDV/r but was equally efficacious. Maxcmin 2 is currently underway evaluating SQV/r vs LPV/r
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(Poster no. WeOrB1265)
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Chan P, Dragsted UB, Pedersen C et al. Maxcmin 1 compared SQV/r withIDV/r and found that SQV/r was better tolerated the IDV/r but was equally efficacious. Maxcmin 2 is currently underway evaluating SQV/r vs LPV/r. XIV Internat. AIDS Conf. (2002) (Poster no. WeOrB1265).
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XIV Internat. AIDS Conf.
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Chan, P.1
Dragsted, U.B.2
Pedersen, C.3
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57
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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) versus Saquinavir/ritonavir (1000/100 mg BID) in adult HIV-1 infection: The MaxCmin2 trial
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2nd IAS Paris France (Abstract LB23)
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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) versus Saquinavir/ritonavir (1000/100 mg BID) in adult HIV-1 infection: the MaxCmin2 trial. 2nd IAS, Paris, France (2003) (Abstract LB23).
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(2003)
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Youle, M.1
Gerstoft, J.2
Fox, Z.3
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58
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85039536230
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Antiviral efficacy, metabolic changes and safety of atazanavir versus lopinavir/ritonavir in combination with 2 NRTIs in patients who have experienced virologic failure with prior PI-containing regimen(s): 24-week results from BMS AI424-043
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2nd IAS (Abstract no. 117)
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Nieto-Cisneros L, Zala C, Fessel WJ et al. Antiviral efficacy, metabolic changes and safety of atazanavir versus lopinavir/ritonavir in combination with 2 NRTIs in patients who have experienced virologic failure with prior PI-containing regimen(s): 24-week results from BMS AI424-043. 2nd IAS (Abstract no. 117).
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Nieto-Cisneros, L.1
Zala, C.2
Fessel, W.J.3
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59
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0037684348
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The context study: Efficacy and safety of GW433908/RTV in PI-experienced subjects with virological failure (24 week results)
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(Abstract 178)
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DeJesus E, LaMarca A, Sension M, Beltran C, Yeni P. The context study: efficacy and safety of GW433908/RTV in PI-experienced subjects with virological failure (24 week results). 10th Conf. Retroviruses Opp. Infect. (2003) (Abstract 178).
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10th Conf. Retroviruses Opp. Infect.
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DeJesus, E.1
LaMarca, A.2
Sension, M.3
Beltran, C.4
Yeni, P.5
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60
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85039520882
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Lack of resistance to boosted 908 confirmed through 48 weeks of therapy in naïve subjects
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2nd IAS (Abstract no. 558)
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Elston R, MacManus S, Yates P et al. Lack of resistance to boosted 908 confirmed through 48 weeks of therapy in naïve subjects. 2nd IAS (Abstract no. 558).
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Elston, R.1
MacManus, S.2
Yates, P.3
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61
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33444467485
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The LOPSAQ study: 24 week analysis of the double protease inhibitor salvage regimen containing lopinavir/ritonavir plus saquinavir without any additional antiretroviral therapy
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2nd IAS Paris France (Abstract no. 583)
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Staszewski S, Dauer B, Von Hentig N et al. The LOPSAQ study: 24 week analysis of the double protease inhibitor salvage regimen containing lopinavir/ritonavir plus saquinavir without any additional antiretroviral therapy. 2nd IAS Paris, France (2003) (Abstract no. 583).
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(2003)
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Staszewski, S.1
Dauer, B.2
Von Hentig, N.3
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62
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85039526591
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Salvage therapy with lopinavir/ritonavir, amprenavir +/- an additional boost with ritonavir: 1-year results of puzzle 1-ANRS 104 study
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2nd IAS Paris France (Abstract no. 585)
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Raguin G, Chene G, Morand-Joubert L et al. Salvage therapy with lopinavir/ritonavir, amprenavir +/- an additional boost with ritonavir: 1-year results of puzzle 1-ANRS 104 study. 2nd IAS Paris, France (2003) (Abstract no. 585).
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(2003)
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Raguin, G.1
Chene, G.2
Morand-Joubert, L.3
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