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Volumn 12, Issue 7, 2012, Pages 550-560

Optimising the manufacture, formulation, and dose of antiretroviral drugs for more cost-efficient delivery in resource-limited settings: A consensus statement

Author keywords

[No Author keywords available]

Indexed keywords

ANTIRETROVIRUS AGENT; ATAZANAVIR; ATAZANAVIR PLUS RITONAVIR; DARUNAVIR; DARUNAVIR PLUS RITONAVIR; DOLUTEGRAVIR; EFAVIRENZ; ELVUCITABINE; FOSAMPRENAVIR; LAMIVUDINE; LOPINAVIR PLUS RITONAVIR; NEVIRAPINE; PLACEBO; RALTEGRAVIR; RILPIVIRINE; RITONAVIR; RITONAVIR PLUS SAQUINAVIR; SAQUINAVIR; STAVUDINE; TENOFOVIR 3 HEXADECYLOXYPROPYL ESTER; ZIDOVUDINE;

EID: 84862752706     PISSN: 14733099     EISSN: 14744457     Source Type: Journal    
DOI: 10.1016/S1473-3099(12)70134-2     Document Type: Review
Times cited : (37)

References (72)
  • 3
    • 84873072980 scopus 로고    scopus 로고
    • Clinton Health Access Initiative, (accessed Feb 17, 2012).
    • Conference on antiretroviral dose optimization: meeting summary Clinton Health Access Initiative, (accessed Feb 17, 2012). http://www.clintonhealthaccess.org/news-and-information/CADO-meeting-summary.
    • Conference on antiretroviral dose optimization: meeting summary
  • 5
    • 78249258110 scopus 로고    scopus 로고
    • Dose optimisation: a strategy to improve tolerability and lower antiretroviral drug prices in low and middle income countries
    • Hill A, Ananworanich J, Calmy A Dose optimisation: a strategy to improve tolerability and lower antiretroviral drug prices in low and middle income countries. Open Infect Dis J 2010, 4:85-91.
    • (2010) Open Infect Dis J , vol.4 , pp. 85-91
    • Hill, A.1    Ananworanich, J.2    Calmy, A.3
  • 6
    • 0025238899 scopus 로고
    • Zidovudine in asymptomatic human immunodeficiency virus infection. A controlled trial in persons with fewer than 500 CD4-positive cells per cubic millimeter. The AIDS Clinical Trials Group of the National Institute of Allergy and Infectious Diseases
    • Volberding PA, Lagakos SW, Koch MA, et al. Zidovudine in asymptomatic human immunodeficiency virus infection. A controlled trial in persons with fewer than 500 CD4-positive cells per cubic millimeter. The AIDS Clinical Trials Group of the National Institute of Allergy and Infectious Diseases. N Engl J Med 1990, 322:941-949.
    • (1990) N Engl J Med , vol.322 , pp. 941-949
    • Volberding, P.A.1    Lagakos, S.W.2    Koch, M.A.3
  • 7
    • 0035922595 scopus 로고    scopus 로고
    • Prevalence of adverse events associated with potent antiretroviral treatment: Swiss HIV Cohort Study
    • Fellay J, Boubaker K, Ledergerber B, et al. Prevalence of adverse events associated with potent antiretroviral treatment: Swiss HIV Cohort Study. Lancet 2001, 358:1322-1327.
    • (2001) Lancet , vol.358 , pp. 1322-1327
    • Fellay, J.1    Boubaker, K.2    Ledergerber, B.3
  • 8
    • 33847353726 scopus 로고    scopus 로고
    • Conservation of first-line antiretroviral treatment regimen where therapeutic options are limited
    • Orrell C, Harling G, Lawn SD, et al. Conservation of first-line antiretroviral treatment regimen where therapeutic options are limited. Antivir Ther 2007, 12:83-88.
    • (2007) Antivir Ther , vol.12 , pp. 83-88
    • Orrell, C.1    Harling, G.2    Lawn, S.D.3
  • 10
    • 70350114055 scopus 로고    scopus 로고
    • Antiretroviral adherence and pharmacokinetics: review of their roles in sustained virologic suppression
    • Pham PA Antiretroviral adherence and pharmacokinetics: review of their roles in sustained virologic suppression. AIDS Patient Care STDS 2009, 23:803-807.
    • (2009) AIDS Patient Care STDS , vol.23 , pp. 803-807
    • Pham, P.A.1
  • 11
    • 0034457843 scopus 로고    scopus 로고
    • Factors affecting adherence to antiretroviral therapy
    • Chesney MA Factors affecting adherence to antiretroviral therapy. Clin Infect Dis 2000, 30(suppl 2):S171-S176.
    • (2000) Clin Infect Dis , vol.30 , Issue.SUPPL. 2
    • Chesney, M.A.1
  • 12
    • 0037284154 scopus 로고    scopus 로고
    • HIV viral suppression in the era of antiretroviral therapy
    • Thaker HK, Snow MH HIV viral suppression in the era of antiretroviral therapy. Postgrad Med J 2003, 79:36-42.
    • (2003) Postgrad Med J , vol.79 , pp. 36-42
    • Thaker, H.K.1    Snow, M.H.2
  • 13
    • 46449097695 scopus 로고    scopus 로고
    • Early loss of HIV-infected patients on potent antiretroviral therapy programmes in lower-income countries
    • Brinkhof MWG, Dabis F, Myer L, et al. Early loss of HIV-infected patients on potent antiretroviral therapy programmes in lower-income countries. Bull World Health Organ 2008, 86:559-567.
    • (2008) Bull World Health Organ , vol.86 , pp. 559-567
    • Brinkhof, M.W.G.1    Dabis, F.2    Myer, L.3
  • 17
    • 84873076407 scopus 로고    scopus 로고
    • Failure on first line therapy and inequalities in switching to second line in adults treated in urban and rural ART programs: multicentric analysis in 28 MSF-supported African and Asian sites. 18th International Aids Conference; Vienna, Austria; July 18-23, 2010.
    • Pujades-Rodrigues M, Ferreyra C, Calmy A, Balkan S. Failure on first line therapy and inequalities in switching to second line in adults treated in urban and rural ART programs: multicentric analysis in 28 MSF-supported African and Asian sites. 18th International Aids Conference; Vienna, Austria; July 18-23, 2010.
    • Pujades-Rodrigues, M.1    Ferreyra, C.2    Calmy, A.3    Balkan, S.4
  • 18
    • 84862735309 scopus 로고    scopus 로고
    • Prolonged delay to switching to second-line therapy in the South African antiretroviral program. 18th International Aids Conference; Vienna, Austria; July 18-23.
    • Osih Y, Murdoch D, Wallis C, Gay C, Venter F. Prolonged delay to switching to second-line therapy in the South African antiretroviral program. 18th International Aids Conference; Vienna, Austria; July 18-23, 2010.
    • (2010)
    • Osih, Y.1    Murdoch, D.2    Wallis, C.3    Gay, C.4    Venter, F.5
  • 19
    • 49449099010 scopus 로고    scopus 로고
    • Emergence of drug resistance in HIV type 1-infected patients after receipt of first-line highly active antiretroviral therapy: a systematic review of clinical trials
    • Gupta R, Hill A, Sawyer AW, Pillay D Emergence of drug resistance in HIV type 1-infected patients after receipt of first-line highly active antiretroviral therapy: a systematic review of clinical trials. Clin Infect Dis 2008, 47:712-722.
    • (2008) Clin Infect Dis , vol.47 , pp. 712-722
    • Gupta, R.1    Hill, A.2    Sawyer, A.W.3    Pillay, D.4
  • 21
    • 79953740157 scopus 로고    scopus 로고
    • Treatment 2.0: catalysing the next phase of scale-up
    • Hirnschall G, Schwartländer B Treatment 2.0: catalysing the next phase of scale-up. Lancet 2011, 378:209-211.
    • (2011) Lancet , vol.378 , pp. 209-211
    • Hirnschall, G.1    Schwartländer, B.2
  • 22
    • 10844220976 scopus 로고    scopus 로고
    • US Department of Health and Human Services, Food and Drug AdministrationFood and Drug Administration, Center for Drug Evaluation and ResearchCenter for Drug Evaluation and Research, Center for Biologics Evaluation and ResearchCenter for Biologics Evaluation and Research, (accessed Feb 2, 2012).
    • Guidance for industry: Q7A good manufacturing practice guidance for active pharmaceutical ingredients US Department of Health and Human Services, Food and Drug AdministrationFood and Drug Administration, Center for Drug Evaluation and ResearchCenter for Drug Evaluation and Research, Center for Biologics Evaluation and ResearchCenter for Biologics Evaluation and Research, (accessed Feb 2, 2012). http://www.fda.gov/downloads/regulatoryinformation/guidances/ucm129098.pdf.
    • Guidance for industry: Q7A good manufacturing practice guidance for active pharmaceutical ingredients
  • 23
    • 0009872542 scopus 로고    scopus 로고
    • US Department of Health and Human Services, Food and Drug AdministrationFood and Drug Administration, Center for Drug Evaluation and ResearchCenter for Drug Evaluation and Research, (accessed Feb 8, 2012).
    • Guidance for industry: changes to an approved NDA or ANDA US Department of Health and Human Services, Food and Drug AdministrationFood and Drug Administration, Center for Drug Evaluation and ResearchCenter for Drug Evaluation and Research, (accessed Feb 8, 2012). http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM077097.pdf.
    • Guidance for industry: changes to an approved NDA or ANDA
  • 28
    • 77957721344 scopus 로고    scopus 로고
    • Tenofovir for the developing world, ACS meeting news: process chemists rework synthesis of anti-HIV drug to lower its cost
    • Halford B Tenofovir for the developing world, ACS meeting news: process chemists rework synthesis of anti-HIV drug to lower its cost. Chem Eng News 2010, 88:58-59.
    • (2010) Chem Eng News , vol.88 , pp. 58-59
    • Halford, B.1
  • 29
    • 77956931336 scopus 로고    scopus 로고
    • Process improvements for the manufacture of tenofovir disoproxil fumarate at commercial scale
    • Brown Ripin DH, Teager DS, Fortunak J, et al. Process improvements for the manufacture of tenofovir disoproxil fumarate at commercial scale. Org Process Res Dev 2010, 14:1194-1201.
    • (2010) Org Process Res Dev , vol.14 , pp. 1194-1201
    • Brown Ripin, D.H.1    Teager, D.S.2    Fortunak, J.3
  • 30
    • 77956613658 scopus 로고    scopus 로고
    • Rapid, mild method for phosphonate diester hydrolysis: development of a one-pot synthesis of tenofovir disoproxil fumarate from tenofovir diethyl ester
    • Houghton SR, Melton J, Fortunak J, Brown Ripin DH, Boddy CN Rapid, mild method for phosphonate diester hydrolysis: development of a one-pot synthesis of tenofovir disoproxil fumarate from tenofovir diethyl ester. Tetrahedron 2010, 66:8137-8144.
    • (2010) Tetrahedron , vol.66 , pp. 8137-8144
    • Houghton, S.R.1    Melton, J.2    Fortunak, J.3    Brown Ripin, D.H.4    Boddy, C.N.5
  • 31
    • 84873069186 scopus 로고    scopus 로고
    • Asymmetric synthesis of (-)6-chloro-4-cyclopropyl-ethynyl-4-trifluoromethyl-1,4-dihydro-2H-3,1-b enzoxazin-2-one. &
    • Thompson AS, Corley EG, Grabowski EJJ, Yasuda N. Asymmetric synthesis of (-)6-chloro-4-cyclopropyl-ethynyl-4-trifluoromethyl-1,4-dihydro-2H-3,1-b enzoxazin-2-one. http://patft.uspto.gov/netacgi/nph-Parser?Sect1=PTO2&Sect2=HITOFF&p=1&u=%2Fnetahtml%2FPTO%2Fsearch-bool.html&r=1&f=G&l=50&co1=AND&d=PTXT&s1=5698741.PN.&OS=PN/5698741&RS=PN/5698741 (accessed Feb 1, 2012).
    • Thompson, A.S.1    Corley, E.G.2    Grabowski, E.J.J.3    Yasuda, N.4
  • 34
    • 84857617880 scopus 로고    scopus 로고
    • Absorption enhancers: applications and advances
    • Aungst BJ Absorption enhancers: applications and advances. AAPS J 2012, 14:10-18.
    • (2012) AAPS J , vol.14 , pp. 10-18
    • Aungst, B.J.1
  • 35
    • 84873069145 scopus 로고    scopus 로고
    • US FDA. Center for Drug Evaluation and Research, (accessed March 29, 2011).
    • US FDA NDA application number 21-906: medical review, 2005 Center for Drug Evaluation and Research, (accessed March 29, 2011). http://www.accessdata.fda.gov/drugsatfda_docs/nda/2005/021906s000_MedR.pdf.
    • NDA application number 21-906: medical review, 2005
  • 36
    • 34147176581 scopus 로고    scopus 로고
    • The tablet formulation of lopinavir/ritonavir provides similar bioavailability to the soft-gelatin capsule formulation with less pharmacokinetic variability and diminished food effect
    • Klein CE, Chiu Y-L, Awni W, et al. The tablet formulation of lopinavir/ritonavir provides similar bioavailability to the soft-gelatin capsule formulation with less pharmacokinetic variability and diminished food effect. J Acquir Immune Defic Syndr 2007, 44:401-410.
    • (2007) J Acquir Immune Defic Syndr , vol.44 , pp. 401-410
    • Klein, C.E.1    Chiu, Y.-L.2    Awni, W.3
  • 37
    • 84873066767 scopus 로고    scopus 로고
    • Comparison of 48 week efficacy and safety of 400mg QD nevirapine extended release formulation (Viramune XR) versus 200mg BID nevirapine immediate release formulation (Viramune IR) in combination with Truvada in antiretroviral (ARV) naïve HIV-1 infected patients (VERxVE). 18th International Aids Conference; Vienna, Austria; July 18thomampersan
    • Gathe J, Bogner J, Santiago S, et al. Comparison of 48 week efficacy and safety of 400mg QD nevirapine extended release formulation (Viramune XR) versus 200mg BID nevirapine immediate release formulation (Viramune IR) in combination with Truvada in antiretroviral (ARV) naïve HIV-1 infected patients (VERxVE). 18th International Aids Conference; Vienna, Austria; July 18-23, 2010.
    • Gathe, J.1    Bogner, J.2    Santiago, S.3
  • 38
    • 78650232840 scopus 로고    scopus 로고
    • Continual reassessment and related dose-finding designs
    • O'Quigley J, Conaway M Continual reassessment and related dose-finding designs. Stat Sci 2010, 25:202-216.
    • (2010) Stat Sci , vol.25 , pp. 202-216
    • O'Quigley, J.1    Conaway, M.2
  • 39
    • 73649148381 scopus 로고    scopus 로고
    • Efficacy and safety of TMC278 in antiretroviral-naive HIV-1 patients: week 96 results of a phase IIb randomized trial
    • Pozniak AL, Morales-Ramirez J, Katabira E, et al. Efficacy and safety of TMC278 in antiretroviral-naive HIV-1 patients: week 96 results of a phase IIb randomized trial. AIDS 2010, 24:55-65.
    • (2010) AIDS , vol.24 , pp. 55-65
    • Pozniak, A.L.1    Morales-Ramirez, J.2    Katabira, E.3
  • 40
    • 79960358849 scopus 로고    scopus 로고
    • Rilpivirine versus efavirenz with two background nucleoside or nucleotide reverse transcriptase inhibitors in treatment-naive adults infected with HIV-1 (THRIVE): a phase 3, randomised, non-inferiority trial
    • Cohen CJ, Andrade-Villanueva J, Clotet B, et al. Rilpivirine versus efavirenz with two background nucleoside or nucleotide reverse transcriptase inhibitors in treatment-naive adults infected with HIV-1 (THRIVE): a phase 3, randomised, non-inferiority trial. Lancet 2011, 378:229-237.
    • (2011) Lancet , vol.378 , pp. 229-237
    • Cohen, C.J.1    Andrade-Villanueva, J.2    Clotet, B.3
  • 41
    • 79960381844 scopus 로고    scopus 로고
    • Rilpivirine versus efavirenz with tenofovir and emtricitabine in treatment-naive adults infected with HIV-1 (ECHO): a phase 3 randomised double-blind active-controlled trial
    • Molina J-M, Cahn P, Grinsztejn B, et al. Rilpivirine versus efavirenz with tenofovir and emtricitabine in treatment-naive adults infected with HIV-1 (ECHO): a phase 3 randomised double-blind active-controlled trial. Lancet 2011, 378:238-246.
    • (2011) Lancet , vol.378 , pp. 238-246
    • Molina, J.-M.1    Cahn, P.2    Grinsztejn, B.3
  • 42
    • 84862777419 scopus 로고    scopus 로고
    • Efficacy and safety of rilpivirine (TMC278) versus efavirenz at 48 weeks in treatment-naive HIV-1-infected patients: pooled results from the phase 3 double-blind randomized ECHO and THRIVE trials
    • Cohen CJ, Molina J-M, Cahn P, et al. Efficacy and safety of rilpivirine (TMC278) versus efavirenz at 48 weeks in treatment-naive HIV-1-infected patients: pooled results from the phase 3 double-blind randomized ECHO and THRIVE trials. J Acquir Immune Defic Syndr 2012, 60:33-42.
    • (2012) J Acquir Immune Defic Syndr , vol.60 , pp. 33-42
    • Cohen, C.J.1    Molina, J.-M.2    Cahn, P.3
  • 43
    • 77953719289 scopus 로고    scopus 로고
    • Generic and low dose antiretroviral therapy in adults and children: implication for scaling up treatment in resource limited settings
    • Ramautarsing R, Ananworanich J Generic and low dose antiretroviral therapy in adults and children: implication for scaling up treatment in resource limited settings. AIDS Res Ther 2010, 7:18.
    • (2010) AIDS Res Ther , vol.7 , pp. 18
    • Ramautarsing, R.1    Ananworanich, J.2
  • 44
    • 0033941723 scopus 로고    scopus 로고
    • A randomized, dose-finding study with didanosine plus stavudine versus didanosine alone in antiviral-naive, HIV-infected Thai patients
    • Ruxrungtham K, Kroon ED, Ungsedhapand C, et al. A randomized, dose-finding study with didanosine plus stavudine versus didanosine alone in antiviral-naive, HIV-infected Thai patients. AIDS 2000, 14:1375-1382.
    • (2000) AIDS , vol.14 , pp. 1375-1382
    • Ruxrungtham, K.1    Kroon, E.D.2    Ungsedhapand, C.3
  • 45
    • 34047193054 scopus 로고    scopus 로고
    • Systematic review of clinical trials evaluating low doses of stavudine as part of antiretroviral treatment
    • Hill A, Ruxrungtham K, Hanvanich M, et al. Systematic review of clinical trials evaluating low doses of stavudine as part of antiretroviral treatment. Expert Opin Pharmacother 2007, 8:679-688.
    • (2007) Expert Opin Pharmacother , vol.8 , pp. 679-688
    • Hill, A.1    Ruxrungtham, K.2    Hanvanich, M.3
  • 46
    • 33745910844 scopus 로고    scopus 로고
    • Intensive pharmacokinetics of zidovudine 200 mg twice daily in HIV-1-infected patients weighing less than 60 kg on highly active antiretroviral therapy
    • Cressey TR, Leenasirimakul P, Jourdain G, Tawon Y, Sukrakanchana P-O, Lallemant M Intensive pharmacokinetics of zidovudine 200 mg twice daily in HIV-1-infected patients weighing less than 60 kg on highly active antiretroviral therapy. J Acquir Immune Defic Syndr 2006, 42:387-389.
    • (2006) J Acquir Immune Defic Syndr , vol.42 , pp. 387-389
    • Cressey, T.R.1    Leenasirimakul, P.2    Jourdain, G.3    Tawon, Y.4    Sukrakanchana, P.-O.5    Lallemant, M.6
  • 47
    • 84873071553 scopus 로고    scopus 로고
    • Efficacy and safety of half dose compared to full dose stavudine (d4T) and zidovudine (AZT) in combination with didanosine (ddI) in Thai HIV-infected patients: 96 weeks results of ACTT002/ARV065 study. 15th International AIDS Conference; Bangkok, Thailand; July 11-16, 2004.
    • Usiangphoe S, Srikaew S, Waiwaravuth C, et al. Efficacy and safety of half dose compared to full dose stavudine (d4T) and zidovudine (AZT) in combination with didanosine (ddI) in Thai HIV-infected patients: 96 weeks results of ACTT002/ARV065 study. 15th International AIDS Conference; Bangkok, Thailand; July 11-16, 2004.
    • Usiangphoe, S.1    Srikaew, S.2    Waiwaravuth, C.3
  • 48
    • 84857183342 scopus 로고    scopus 로고
    • Pharmacokinetics of lamivudine, and lamivudine-triphosphate after administration of 300 mg and 150 mg once-daily to healthy volunteers. The ENCORE 2 Study
    • Else LJ, Jackson A, Puls R, et al. Pharmacokinetics of lamivudine, and lamivudine-triphosphate after administration of 300 mg and 150 mg once-daily to healthy volunteers. The ENCORE 2 Study. Antimicrob Agents Chemother 2012, 56:1427-1433.
    • (2012) Antimicrob Agents Chemother , vol.56 , pp. 1427-1433
    • Else, L.J.1    Jackson, A.2    Puls, R.3
  • 49
    • 84873070277 scopus 로고    scopus 로고
    • A phase II, double-blind, placebo-controlled, dose ranging study to assess the antiretroviral activity and safety of DMP 266 (efavirenz, Sustiva™) in combination with open-label zidovudine (ZDV) with lamivudine (3TC) [DMP 266-005]. 5th Conference on Retroviruses and Opportunistic Infections; Chicago, IL, USA; Feb 1-5, 1998. A
    • Hicks C, Hass D, Seekins D, et al. A phase II, double-blind, placebo-controlled, dose ranging study to assess the antiretroviral activity and safety of DMP 266 (efavirenz, Sustiva™) in combination with open-label zidovudine (ZDV) with lamivudine (3TC) [DMP 266-005]. 5th Conference on Retroviruses and Opportunistic Infections; Chicago, IL, USA; Feb 1-5, 1998. Abstract 698.
    • Hicks, C.1    Hass, D.2    Seekins, D.3
  • 50
    • 17044457875 scopus 로고    scopus 로고
    • ABT-378/ritonavir plus stavudine and lamivudine for the treatment of antiretroviral-naive adults with HIV-1 infection: 48-week results
    • Murphy RL, Brun S, Hicks C, et al. ABT-378/ritonavir plus stavudine and lamivudine for the treatment of antiretroviral-naive adults with HIV-1 infection: 48-week results. AIDS 2001, 15:F1-F9.
    • (2001) AIDS , vol.15
    • Murphy, R.L.1    Brun, S.2    Hicks, C.3
  • 51
    • 79951527317 scopus 로고    scopus 로고
    • Pharmacokinetics of plasma lopinavir/ritonavir following the administration of 400/100 mg, 200/150 mg and 200/50 mg twice daily in HIV-negative volunteers
    • Jackson A, Hill A, Puls R, et al. Pharmacokinetics of plasma lopinavir/ritonavir following the administration of 400/100 mg, 200/150 mg and 200/50 mg twice daily in HIV-negative volunteers. J Antimicrob Chemother 2011, 66:635-640.
    • (2011) J Antimicrob Chemother , vol.66 , pp. 635-640
    • Jackson, A.1    Hill, A.2    Puls, R.3
  • 52
    • 67651085606 scopus 로고    scopus 로고
    • Reducing the boosting dose of ritonavir does not affect saquinavir plasma concentrations in HIV-1-infected individuals
    • van der Lugt J, Gorowara M, Avihingsanon A, et al. Reducing the boosting dose of ritonavir does not affect saquinavir plasma concentrations in HIV-1-infected individuals. AIDS 2009, 23:1176-1179.
    • (2009) AIDS , vol.23 , pp. 1176-1179
    • van der Lugt, J.1    Gorowara, M.2    Avihingsanon, A.3
  • 53
    • 70449440262 scopus 로고    scopus 로고
    • How much ritonavir is needed to boost protease inhibitors? Systematic review of 17 dose-ranging pharmacokinetic trials
    • Hill A, van der Lugt J, Sawyer W, Boffito M How much ritonavir is needed to boost protease inhibitors? Systematic review of 17 dose-ranging pharmacokinetic trials. AIDS 2009, 23:2237-2245.
    • (2009) AIDS , vol.23 , pp. 2237-2245
    • Hill, A.1    van der Lugt, J.2    Sawyer, W.3    Boffito, M.4
  • 54
    • 84873070794 scopus 로고    scopus 로고
    • No changes in atazanavir exposure when boosted with 50mg or 100mg of ritonavir in healthy volunteers. 12th International Workshop on Clinical Pharmacology of HIV Therapy; Miami, FL, USA; April 13-15, 2011. Abstract P_31.
    • Estevez J, Molto J, Tuneu L, et al. No changes in atazanavir exposure when boosted with 50mg or 100mg of ritonavir in healthy volunteers. 12th International Workshop on Clinical Pharmacology of HIV Therapy; Miami, FL, USA; April 13-15, 2011. Abstract P_31.
    • Estevez, J.1    Molto, J.2    Tuneu, L.3
  • 55
    • 62649107112 scopus 로고    scopus 로고
    • A low dose of ritonavir-boosted atazanavir provides adequate pharmacokinetic parameters in HIV-1-infected Thai adults
    • Avihingsanon A, van der Lugt J, Kerr SJ, et al. A low dose of ritonavir-boosted atazanavir provides adequate pharmacokinetic parameters in HIV-1-infected Thai adults. Clin Pharmacol Ther 2009, 85:402-408.
    • (2009) Clin Pharmacol Ther , vol.85 , pp. 402-408
    • Avihingsanon, A.1    van der Lugt, J.2    Kerr, S.J.3
  • 56
    • 33847041109 scopus 로고    scopus 로고
    • Efficacy and safety of TMC114/ritonavir in treatment-experienced HIV patients: 24-week results of POWER 1
    • Katlama C, Esposito R, Gatell JM, et al. Efficacy and safety of TMC114/ritonavir in treatment-experienced HIV patients: 24-week results of POWER 1. AIDS 2007, 21:395-402.
    • (2007) AIDS , vol.21 , pp. 395-402
    • Katlama, C.1    Esposito, R.2    Gatell, J.M.3
  • 57
    • 34748860363 scopus 로고    scopus 로고
    • Rapid and durable antiretroviral effect of the HIV-1 integrase inhibitor raltegravir as part of combination therapy in treatment-naive patients with HIV-1 infection: results of a 48-week controlled study
    • Markowitz M, Nguyen B-Y, Gotuzzo E, et al. Rapid and durable antiretroviral effect of the HIV-1 integrase inhibitor raltegravir as part of combination therapy in treatment-naive patients with HIV-1 infection: results of a 48-week controlled study. J Acquir Immune Defic Syndr 2007, 46:125-133.
    • (2007) J Acquir Immune Defic Syndr , vol.46 , pp. 125-133
    • Markowitz, M.1    Nguyen, B.-Y.2    Gotuzzo, E.3
  • 58
    • 1542376227 scopus 로고    scopus 로고
    • Pharmacodynamic effects of zidovudine 600 mg once/day versus 300 mg twice/day in therapy-naïve patients infected with human immunodeficiency virus
    • Ruane PJ, Richmond GJ, DeJesus E, et al. Pharmacodynamic effects of zidovudine 600 mg once/day versus 300 mg twice/day in therapy-naïve patients infected with human immunodeficiency virus. Pharmacotherapy 2004, 24:307-312.
    • (2004) Pharmacotherapy , vol.24 , pp. 307-312
    • Ruane, P.J.1    Richmond, G.J.2    DeJesus, E.3
  • 59
    • 0024405549 scopus 로고
    • Cellular pharmacology of 2',3'-dideoxy-2',3'-didehydrothymidine, a nucleoside analog active against human immunodeficiency virus
    • Ho HT, Hitchcock MJ Cellular pharmacology of 2',3'-dideoxy-2',3'-didehydrothymidine, a nucleoside analog active against human immunodeficiency virus. Antimicrob Agents Chemother 1989, 33:844-849.
    • (1989) Antimicrob Agents Chemother , vol.33 , pp. 844-849
    • Ho, H.T.1    Hitchcock, M.J.2
  • 60
    • 0033790624 scopus 로고    scopus 로고
    • Zidovudine triphosphate and lamivudine triphosphate concentration-response relationships in HIV-infected persons
    • Fletcher CV, Kawle SP, Kakuda TN, et al. Zidovudine triphosphate and lamivudine triphosphate concentration-response relationships in HIV-infected persons. AIDS 2000, 14:2137-2144.
    • (2000) AIDS , vol.14 , pp. 2137-2144
    • Fletcher, C.V.1    Kawle, S.P.2    Kakuda, T.N.3
  • 61
    • 0026446188 scopus 로고
    • Intracellular zidovudine (ZDV) and ZDV phosphates as measured by a validated combined high-pressure liquid chromatography-radioimmunoassay procedure
    • Slusher JT, Kuwahara SK, Hamzeh FM, Lewis LD, Kornhauser DM, Lietman PS Intracellular zidovudine (ZDV) and ZDV phosphates as measured by a validated combined high-pressure liquid chromatography-radioimmunoassay procedure. Antimicrob Agents Chemother 1992, 36:2473-2477.
    • (1992) Antimicrob Agents Chemother , vol.36 , pp. 2473-2477
    • Slusher, J.T.1    Kuwahara, S.K.2    Hamzeh, F.M.3    Lewis, L.D.4    Kornhauser, D.M.5    Lietman, P.S.6
  • 62
    • 33746866382 scopus 로고    scopus 로고
    • Model for intracellular Lamivudine metabolism in peripheral blood mononuclear cells ex vivo and in human immunodeficiency virus type 1-infected adolescents
    • Zhou Z, Rodman JH, Flynn PM, Robbins BL, Wilcox CK, D'Argenio DZ Model for intracellular Lamivudine metabolism in peripheral blood mononuclear cells ex vivo and in human immunodeficiency virus type 1-infected adolescents. Antimicrob Agents Chemother 2006, 50:2686-2694.
    • (2006) Antimicrob Agents Chemother , vol.50 , pp. 2686-2694
    • Zhou, Z.1    Rodman, J.H.2    Flynn, P.M.3    Robbins, B.L.4    Wilcox, C.K.5    D'Argenio, D.Z.6
  • 64
    • 62649093555 scopus 로고    scopus 로고
    • Pharmacokinetics, efficacy, and safety of darunavir/ritonavir 800/100 mg once-daily in treatment-naïve and -experienced patients
    • Boffito M, Miralles D, Hill A Pharmacokinetics, efficacy, and safety of darunavir/ritonavir 800/100 mg once-daily in treatment-naïve and -experienced patients. HIV Clin Trials 2008, 9:418-427.
    • (2008) HIV Clin Trials , vol.9 , pp. 418-427
    • Boffito, M.1    Miralles, D.2    Hill, A.3
  • 65
    • 81855166275 scopus 로고    scopus 로고
    • Raltegravir once daily or twice daily in previously untreated patients with HIV-1: a randomised, active-controlled, phase 3 non-inferiority trial
    • Eron JJ, Rockstroh JK, Reynes J, et al. Raltegravir once daily or twice daily in previously untreated patients with HIV-1: a randomised, active-controlled, phase 3 non-inferiority trial. Lancet Infect Dis 2011, 11:907-915.
    • (2011) Lancet Infect Dis , vol.11 , pp. 907-915
    • Eron, J.J.1    Rockstroh, J.K.2    Reynes, J.3
  • 66
    • 0346025675 scopus 로고    scopus 로고
    • Pharmacological and therapeutic properties of ritonavir-boosted protease inhibitor therapy in HIV-infected patients
    • Zeldin RK, Petruschke RA Pharmacological and therapeutic properties of ritonavir-boosted protease inhibitor therapy in HIV-infected patients. J Antimicrob Chemother 2004, 53:4-9.
    • (2004) J Antimicrob Chemother , vol.53 , pp. 4-9
    • Zeldin, R.K.1    Petruschke, R.A.2
  • 67
    • 84873072231 scopus 로고    scopus 로고
    • QDMRK, a phase III study of the safety and efficacy of once daily vs twice daily RAL in combination therapy for treatment-naïve HIV-infected patients. 18th Conference on Retroviruses and Opportunistic Infections; Boston, MA, USA; Feb 27-March 2, 2011. Abstract 42603.
    • Eron J, Rockstroh J, Reynes J, et al. QDMRK, a phase III study of the safety and efficacy of once daily vs twice daily RAL in combination therapy for treatment-naïve HIV-infected patients. 18th Conference on Retroviruses and Opportunistic Infections; Boston, MA, USA; Feb 27-March 2, 2011. Abstract 42603.
    • Eron, J.1    Rockstroh, J.2    Reynes, J.3
  • 68
    • 77149123315 scopus 로고    scopus 로고
    • Pharmacokinetics and pharmacodynamics of GS-9350: a novel pharmacokinetic enhancer without anti-HIV activity
    • Mathias AA, German P, Murray BP, et al. Pharmacokinetics and pharmacodynamics of GS-9350: a novel pharmacokinetic enhancer without anti-HIV activity. Clin Pharmacol Ther 2010, 87:322-329.
    • (2010) Clin Pharmacol Ther , vol.87 , pp. 322-329
    • Mathias, A.A.1    German, P.2    Murray, B.P.3
  • 69
    • 33748113778 scopus 로고    scopus 로고
    • Antiviral activity, pharmacokinetics, and dose response of the HIV-1 integrase inhibitor GS-9137 (JTK-303) in treatment-naive and treatment-experienced patients
    • DeJesus E, Berger D, Markowitz M, et al. Antiviral activity, pharmacokinetics, and dose response of the HIV-1 integrase inhibitor GS-9137 (JTK-303) in treatment-naive and treatment-experienced patients. J Acquir Immune Defic Syndr 2006, 43:1-5.
    • (2006) J Acquir Immune Defic Syndr , vol.43 , pp. 1-5
    • DeJesus, E.1    Berger, D.2    Markowitz, M.3
  • 70
    • 57749197592 scopus 로고    scopus 로고
    • Dose-response of ritonavir on hepatic CYP3A activity and elvitegravir oral exposure
    • Mathias AA, West S, Hui J, Kearney BP Dose-response of ritonavir on hepatic CYP3A activity and elvitegravir oral exposure. Clin Pharmacol Ther 2009, 85:64-70.
    • (2009) Clin Pharmacol Ther , vol.85 , pp. 64-70
    • Mathias, A.A.1    West, S.2    Hui, J.3    Kearney, B.P.4


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