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Panel on antiretroviral guidelines for adults and adolescents
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Department of Health and Human Services. 1st December Accessed 12 October 2010
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Panel on Antiretroviral Guidelines for Adults and Adolescents. Guidelines for the use of antiretroviral agents in HIV-1-infected adults and adolescents. Department of Health and Human Services. 1st December 2009. p. 1-161. Available from: http://www.aidsinfo.nih.gov/ ContentFiles/AdultandAdolescentGL.pdf. [Accessed 12 October 2010]
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Guidelines for the Use of Antiretroviral Agents in HIV-1-infected Adults and Adolescents
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Clinical Management and Treatment of HIV Infected Adults in Europe (Version 5-2)
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5
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0346025675
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Pharmacological and therapeutic properties of ritonavir-boosted protease inhibitor therapy in HIV-infected patients
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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
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Principles and practice of HIV-protease inhibitor pharmacoenhancement
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HIV Med
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Abbott Laboratories. Abbott received U.S. FDA approval for heat-stable Norvir- (ritonavir) tablets. 11th February 2010. Available from: http://www.abbott.com/ global/url/pressRelease/en-US/60.5:5/ Press-Release-0820.htm [Accessed 12 October 2010]
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Abbott Received U.S. FDA Approval for Heat-stable Norvir- (Ritonavir) Tablets
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8
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77951205335
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Formation of nano/micro-dispersions with improved dissolution properties upon dispersion of ritonavir melt extrudate in aqueous media
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Tho I, Liepold B, Rosenberg J, et al. Formation of nano/micro-dispersions with improved dissolution properties upon dispersion of ritonavir melt extrudate in aqueous media. Eur J Pharm Sci 2010;40:25-32
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Eur J Pharm Sci
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Tho, I.1
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9
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A comparison of the single dose bioavailability of a ritonavir tablet formulation relative to the ritonavir soft gelatin capsule in healthy adult subjects [abstract TUPE0076]
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8 August Mexico City, Mexico. Poster
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Ng J, Klein C, Causemaker C, et al. A comparison of the single dose bioavailability of a ritonavir tablet formulation relative to the ritonavir soft gelatin capsule in healthy adult subjects [abstract TUPE0076]. 17th International AIDS Conference; 3 - 8 August 2008; Mexico City, Mexico. Poster available from: www.medadvocates.org/resources/ conferences/international-aids- conferences/17/lopinavir-index/17N.pdf
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17th International AIDS Conference
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Ng, J.1
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A Pivotal Biostudy Comparing Ritonavir 100 Mg Film-coated Tablet to A Ritonavir 100 Mg Soft Gelatin Capsule in Healthy Adult Subjects [Abstract THAB04]
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Mexico City, Mexico
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Klein C, Chiu YL, Awni W, et al. A pivotal biostudy comparing ritonavir 100 mg film-coated tablet to a ritonavir 100 mg soft gelatin capsule in healthy adult subjects [abstract THAB04]. 17th International AIDS Conference; 3 - 8 August 2008; Mexico City, Mexico
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17th International AIDS Conference; 3 - 8 August
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Klein, C.1
Chiu, Y.L.2
Awni, W.3
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11
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78650440786
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The effect of food on ritonavir bioavailability following administration of ritonavir 100 mg film-coated tablet in healthy adult subjects [abstractP247]
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Glasgow, Scotland, Poster
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Klein CE, Chiu YL, Awni W, et al. The effect of food on ritonavir bioavailability following administration of ritonavir 100 mg film-coated tablet in healthy adult subjects [abstractP247]. 7th International Congress on Drug Therapy in HIV Infection; 9 - 13 November 2008 Glasgow, Scotland, Poster available from: www. hivandhepatitis.com/2008icr/hiv9/docs/ posters/ KleinRTVtablet.pdf
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7th International Congress on Drug Therapy in HIV Infection; 9 - 13 November
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Klein, C.E.1
Chiu, Y.L.2
Awni, W.3
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14
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34147176581
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The tablet formulation of lopinavir/ritonavir provides similar bioavailability to the soft-gelatin capsule formulation with less pharmacokinetic variability and diminished food effect
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Klein CE, Chiu YL, 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;44:401-10
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Klein, C.E.1
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45249086250
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Study M05-730 Primary efficacy results at week 48: Phase 3, randomized, open-label study of lopinavir/ritonavir tablets once daily vs twice daily, co-administered with tenofovir DF + emtricitabine in ARV-naive HIV-1 infected subjects [abstract 775]
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Boston, MA
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Gathe J, da Silva B, Loutfy M, et al. Study M05-730 Primary efficacy results at week 48: phase 3, randomized, open-label study of lopinavir/ritonavir tablets once daily vs twice daily, co-administered with tenofovir DF + emtricitabine in ARV-naive HIV-1 infected subjects [abstract 775]. 15th Conference on Retroviruses and Opportunistic Infections (CROI). 3 - 6 February 2008. Boston, MA
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15th Conference on Retroviruses and Opportunistic Infections (CROI). 3 -6 February
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Gathe, J.1
Da Silva, B.2
Loutfy, M.3
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16
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53549086680
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Significant improvements in self-reported gastrointestinal tolerability, quality of life, patient satisfaction, and adherence with lopinavir/ritonavir tablet formulation compared with soft gel capsules
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Schrader S, Chuck SK, Rahn LW, et al. Significant improvements in self-reported gastrointestinal tolerability, quality of life, patient satisfaction, and adherence with lopinavir/ritonavir tablet formulation compared with soft gel capsules. AIDS Res Ther 2008;5:21
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AIDS Res Ther
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Schrader, S.1
Chuck, S.K.2
Rahn, L.W.3
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17
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78650478166
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Formulation preference, tolerability and quality of life assessment following a switch from lopinavir/ ritonavir soft gel capsule to tablet in human immunodeficiency virus-infected patients
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Ofotokun I, Chuck SK, Schmotzer B, ONeil KL. Formulation preference, tolerability and quality of life assessment following a switch from lopinavir/ ritonavir soft gel capsule to tablet in human immunodeficiency virus-infected patients. AIDS Res Ther 2009;6:29
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AIDS Res Ther
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Ofotokun, I.1
Chuck, S.K.2
Schmotzer, B.3
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Drug interactions of HIV protease inhibitors
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Malaty LI, Kuper JJ. Drug interactions of HIV protease inhibitors. Drug Saf 1999;20:147-69
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Drug Saf
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Pharmacokinetics and potential interactions amongst antiretroviral agents used to treat patients with HIV infection
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Barry M, Mulcahy F, Merry C, et al. Pharmacokinetics and potential interactions amongst antiretroviral agents used to treat patients with HIV infection. Clin Pharmacokinet 1999;36:289-304
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Clin Pharmacokinet
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Pharmacokinetics and pharmacodynamics of GS-9350: A novel pharmacokinetic enhancer without anti-HIV activity
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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;87:322-9
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Clin Pharmacol Ther
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Mathias, A.A.1
German, P.2
Murray, B.P.3
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21
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83655179996
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The single-tablet regimen elvitegravir/ cobicistat/emtricitabine/ tenofovir disoproxil fumarate (EVG/COBI/FTC/ TDF; QUAD) maintains a high rate of virologic suppression, and cobicistat is an effective pharmacoenhancer through 48 weeks [poster H-938B]
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Boston, MA
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Elion R, Gathe J, Rashbaum B, et al. The single-tablet regimen elvitegravir/ cobicistat/emtricitabine/tenofovir disoproxil fumarate (EVG/COBI/FTC/ TDF; QUAD) maintains a high rate of virologic suppression, and cobicistat is an effective pharmacoenhancer through 48 weeks [poster H-938B]. 50th Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC); 12 - 15 September 2010; Boston, MA
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50th Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC); 12 - 15 September
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Elion, R.1
Gathe, J.2
Rashbaum, B.3
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22
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78049293198
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Pharmacokinetics and bioavailability of an integrase and novel pharmacoenhancer-containing single-tablet fixed-dose combination regimen for the treatment of HIV
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German P, Warren D, West S, et al. Pharmacokinetics and bioavailability of an integrase and novel pharmacoenhancer-containing single-tablet fixed-dose combination regimen for the treatment of HIV. J Acquir Immune Defic Syndr 2010;55(3):323-9
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German, P.1
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Relative bioavailability and pharmacokinetics of darunavir when boosted with the pharmacoenhancer GS-9350 versus ritonavir [abstract 28]
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Sorrento, Italy
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Mathias A, Liu HC, Warren D, et al. Relative bioavailability and pharmacokinetics of darunavir when boosted with the pharmacoenhancer GS-9350 versus ritonavir [abstract 28]. 11th International Workshop on Clinical Pharmacology of HIV Therapy; 7 - 9 April 2010; Sorrento, Italy
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11th International Workshop on Clinical Pharmacology of HIV Therapy; 7 - 9 April
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Mathias, A.1
Liu, H.C.2
Warren, D.3
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24
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78650489246
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Pharmacokinetic boosting of atazanavir with the pharmacoenhancer GS-9350 versus ritonavir [poster A1-1301]
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San Francisco, CA
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Ramanatham S, Warren D, Wei L, Kearney BP. Pharmacokinetic boosting of atazanavir with the pharmacoenhancer GS-9350 versus ritonavir [poster A1-1301]. 49th Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC); 12 - 15 September, 2009 San Francisco, CA
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49th Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC); 12 -15 September
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Ramanatham, S.1
Warren, D.2
Wei, L.3
Kearney, B.P.4
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