BENCHMRK Study Teams. Raltegravir with optimized background therapy for resistant HIV-1 infection
Steigbigel RT, Cooper DA, Kumar PN, et al. BENCHMRK Study Teams. Raltegravir with optimized background therapy for resistant HIV-1 infection. N Engl J Med 2008; 359:339-54.
Long-term efficacy and safety of raltegravir combined with optimized background therapy in treatment-experienced patients with drug-resistant HIV infection: Week 96 results of the BENCHMRK 1 and 2 phase III trials
BENCHMRK Study Teams
Steigbigel RT, Cooper DA, Teppler H, et al. BENCHMRK Study Teams. Long-term efficacy and safety of raltegravir combined with optimized background therapy in treatment-experienced patients with drug-resistant HIV infection: week 96 results of the BENCHMRK 1 and 2 phase III trials. Clin Infect Dis 2010; 50:605-12.
Safety and efficacyofraltegravir-based versus efavirenz-basedcombination therapy in treatment-naive patients with HIV-1 infection: A multicentre, double-blind randomised controlled trial
STARTMRK investigators
Lennox JL, DeJesus E, Lazzarin A, et al. STARTMRK investigators. Safety and efficacyofraltegravir-based versus efavirenz-basedcombination therapy in treatment-naive patients with HIV-1 infection: a multicentre, double-blind randomised controlled trial. Lancet 2009; 374:796-806.
Switch from enfuvirtide to raltegravir in virologically suppressed multi-drug-resistant HIV-1-infected patients: A randomized open-label trial
EASIER ANRS 138 study group
De Castro N, Braun J, Charreau I, et al. EASIER ANRS 138 study group. Switch from enfuvirtide to raltegravir in virologically suppressed multi-drug-resistant HIV-1-infected patients: a randomized open-label trial. Clin Infect Dis 2009; 49:1259-67.
Long-term treatment with raltegravir or efavirenz combined with tenofo-vir/emtricitabine for treatment-naive human immunodeficiency virus-1-infected patients: 156-week results from STARTMRK
STARTMRK Investigators
Rockstroh JK, Lennox JL, Dejesus E, et al., STARTMRK Investigators. Long-term treatment with raltegravir or efavirenz combined with tenofo-vir/emtricitabine for treatment-naive human immunodeficiency virus-1-infected patients: 156-week results from STARTMRK. Clin Infect Dis 2011; 53:807-16.
A sensitive HPLC-MS-MS method for the determination of raltegravir in human plasma
Long MC, Bennetto-Hood C, Acosta EP. A sensitive HPLC-MS-MS method for the determination of raltegravir in human plasma. J Chro-matogr B Analyt Technol Biomed Life Sci 2008; 867:165-71.
Determination of the HIV integrase inhibitor, MK-0518 (raltegravir), in human plasma using 96-well liquid-liquid extraction and HPLC MS/MS
Merschman SA, Vallano PT, Wenning LA, Matuszewski BK, Woolf EJ. Determination of the HIV integrase inhibitor, MK-0518 (raltegravir), in human plasma using 96-well liquid-liquid extraction and HPLC MS/MS. J Chromatogr B Analyt Technol Biomed Life Sci 2007; 857: 15-24.
Pharmacokinetics, safety and efficacy of darunavir/ritonavir in treatment-experienced children and adolescents
Blanche S, Bologna R, Cahn P, et al. Pharmacokinetics, safety and efficacy of darunavir/ritonavir in treatment-experienced children and adolescents. AIDS 2009; 23:2005-13.
Efficacy, safety and tolerability of ti-pranavir coadministered with ritonavir in HIV-1 infected children and adolescents
Salazar JC, Cahn P, Yogev R, et al. Efficacy, safety and tolerability of ti-pranavir coadministered with ritonavir in HIV-1 infected children and adolescents. AIDS 2008; 22:1789-98.