-
1
-
-
44049091402
-
-
Anderson MS, Wenning L, Moreau A, et al. 2007. Effect of raltegravir on the pharmacokinetics of oral contraceptives. 47th Interscience Conference on Antimicrobial Agents and Chemotherapy, Chicago, IL. September 17-20, 2007. Abstract A-1425.
-
Anderson MS, Wenning L, Moreau A, et al. 2007. Effect of raltegravir on the pharmacokinetics of oral contraceptives. 47th Interscience Conference on Antimicrobial Agents and Chemotherapy, Chicago, IL. September 17-20, 2007. Abstract A-1425.
-
-
-
-
2
-
-
44049085285
-
-
Cooper D, Gatell J, Rockstroh J, et al. 2007. Results of BENCHMRK-1, a phase III study evaluating the efficacy and safety of MK-0518, a novel HIV-1 integrase inhibitor, in patients with triple-class resistant virus. Program and abstracts of the 14th Conference on Retroviruses and Opportunistic Infections; February 25-28, 2007; Los Angeles, California. Abstracts 105aLB.
-
Cooper D, Gatell J, Rockstroh J, et al. 2007. Results of BENCHMRK-1, a phase III study evaluating the efficacy and safety of MK-0518, a novel HIV-1 integrase inhibitor, in patients with triple-class resistant virus. Program and abstracts of the 14th Conference on Retroviruses and Opportunistic Infections; February 25-28, 2007; Los Angeles, California. Abstracts 105aLB.
-
-
-
-
3
-
-
0035968306
-
HIV integrase, a brief overview from chemistry to therapeutics
-
Craigie R. 2001. HIV integrase, a brief overview from chemistry to therapeutics. J Biol Chem, 276:23213-6.
-
(2001)
J Biol Chem
, vol.276
, pp. 23213-23216
-
-
Craigie, R.1
-
4
-
-
44049089632
-
-
DeJesus E, Cohen C, Elion R, et al. 2007. First report of raltegravir (RAL, MK-0518) use after virologic rebound on elvitegravir (EVT, GS 9137). Program and abstracts of the 4th International AIDS Society Conference on HIV Pathogenesis, Treatment and Prevention; July 22-25, 2007; Sydney, Australia. Abstract TUPEB032.
-
DeJesus E, Cohen C, Elion R, et al. 2007. First report of raltegravir (RAL, MK-0518) use after virologic rebound on elvitegravir (EVT, GS 9137). Program and abstracts of the 4th International AIDS Society Conference on HIV Pathogenesis, Treatment and Prevention; July 22-25, 2007; Sydney, Australia. Abstract TUPEB032.
-
-
-
-
5
-
-
24344490276
-
A series of 5-(5,6)-dihydrouracil substituted 8-hydroxy-[1,6]naphthyridine-7-carboxylic acid 4-fluorobenzylamide inhibitors of HIV-1 integrase and viral replication in cells
-
Embrey MW, Wai JS, Funk TW, et al. 2005. A series of 5-(5,6)-dihydrouracil substituted 8-hydroxy-[1,6]naphthyridine-7-carboxylic acid 4-fluorobenzylamide inhibitors of HIV-1 integrase and viral replication in cells. Bioorg Med Chem Lett, 15:4550-4.
-
(2005)
Bioorg Med Chem Lett
, vol.15
, pp. 4550-4554
-
-
Embrey, M.W.1
Wai, J.S.2
Funk, T.W.3
-
6
-
-
12944270496
-
HIV-1 integrase inhibitors that compete with the target DNA substrate define a unique strand transfer conformation for integrase
-
Espeseth AS, Felock P, Wolfe A, et al. 2000. HIV-1 integrase inhibitors that compete with the target DNA substrate define a unique strand transfer conformation for integrase. Proc Natl Acad Sci USA, 97:11244-9.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 11244-11249
-
-
Espeseth, A.S.1
Felock, P.2
Wolfe, A.3
-
7
-
-
34147136222
-
Safety and efficacy of the HIV-1 integrase inhibitor raltegravir (MK-0518) in treatment-experienced patients with multidrug-resistant virus: A phase II randomised controlled trial
-
Grinsztejn B, Nguyen B, Katlama C, et al. 2007. Safety and efficacy of the HIV-1 integrase inhibitor raltegravir (MK-0518) in treatment-experienced patients with multidrug-resistant virus: a phase II randomised controlled trial. Lancet, 369:1261-9.
-
(2007)
Lancet
, vol.369
, pp. 1261-1269
-
-
Grinsztejn, B.1
Nguyen, B.2
Katlama, C.3
-
8
-
-
0032922813
-
Isolation and characterization of novel human immunodeficiency virus integrase inhibitors from fungal metabolites
-
Hazuda D, Blau CU, Felock P, et al. 1999. Isolation and characterization of novel human immunodeficiency virus integrase inhibitors from fungal metabolites. Antivir Chem Chemother, 10:63-70.
-
(1999)
Antivir Chem Chemother
, vol.10
, pp. 63-70
-
-
Hazuda, D.1
Blau, C.U.2
Felock, P.3
-
9
-
-
3843108916
-
A naphthyridine carboxamide provides evidence for discordant resistance between mechanistically identical inhibitors of HIV-1 integrase
-
Hazuda DJ, Anthony NJ, Gomez RP, et al. 2004. A naphthyridine carboxamide provides evidence for discordant resistance between mechanistically identical inhibitors of HIV-1 integrase. Proc Natl Acad Sci USA, 101:11233-8.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 11233-11238
-
-
Hazuda, D.J.1
Anthony, N.J.2
Gomez, R.P.3
-
10
-
-
0034723439
-
Inhibitors of strand transfer that prevent integration and inhibit HIV-1 replication in cells
-
Hazuda DJ, Felock P, Witmer M, et al. 2000. Inhibitors of strand transfer that prevent integration and inhibit HIV-1 replication in cells. Science, 287:646-50.
-
(2000)
Science
, vol.287
, pp. 646-650
-
-
Hazuda, D.J.1
Felock, P.2
Witmer, M.3
-
11
-
-
44049095538
-
-
Hazuda DJ, Miller MD, Nguyen BY, et al. 2007. Resistance to the HIV-integrase inhibitor raltegravir: analysis of protocol 005, a phase II study in patients with triple-class-resistant HIV-1 infection. Program and abstracts of the 16th International HIV Drug Resistance Workshop; June 12-16, 2007; Barbados, West Indies. Abstract 8.
-
Hazuda DJ, Miller MD, Nguyen BY, et al. 2007. Resistance to the HIV-integrase inhibitor raltegravir: analysis of protocol 005, a phase II study in patients with triple-class-resistant HIV-1 infection. Program and abstracts of the 16th International HIV Drug Resistance Workshop; June 12-16, 2007; Barbados, West Indies. Abstract 8.
-
-
-
-
12
-
-
44049097603
-
-
Isentress prescribing information. Merck and Co., Iin., Whitehouse Station, NJ 08889, USA.
-
Isentress prescribing information. Merck and Co., Iin., Whitehouse Station, NJ 08889, USA.
-
-
-
-
13
-
-
45849141431
-
-
ISENTRESS™ (raltegravir) 400 mg for treatment of HIV NDA 22-145, Accessed October 15, 2007.URL
-
ISENTRESS™ (raltegravir) 400 mg for treatment of HIV (NDA 22-145) 2007. FDA Briefing Document. Accessed October 15, 2007.URL: http://www.fda.gov/OHRMS/DOCKETS/AC/07/briefing/2007-4314b1-01-Merck.pdf.
-
(2007)
FDA Briefing Document
-
-
-
14
-
-
44049096773
-
-
Iwamoto M, Wenning LA, Liou SY, et al. 2006. Rifampin (RIF) modestly reduces plasma levels of MK-0518. 8th international congress on drug therapy in HIV infection, Glasgow. Nov 2006. Abstract 20061; p299.
-
Iwamoto M, Wenning LA, Liou SY, et al. 2006. Rifampin (RIF) modestly reduces plasma levels of MK-0518. 8th international congress on drug therapy in HIV infection, Glasgow. Nov 2006. Abstract 20061; p299.
-
-
-
-
15
-
-
37249045158
-
Minimal effect of ritonavir (RTV) and efavirenz (EFV) on the pharmacokinetics (PK) ofMK-0518
-
San Francisco, CA, Abstract 2006b;
-
Iwamoto M, Wenning LA, Petry AS et al. 2006. Minimal effect of ritonavir (RTV) and efavirenz (EFV) on the pharmacokinetics (PK) ofMK-0518. 46th Annual ICAAC Meeting. San Francisco, CA, 2006: Abstract 2006b; A-373.
-
(2006)
46th Annual ICAAC Meeting
-
-
Iwamoto, M.1
Wenning, L.A.2
Petry, A.S.3
-
16
-
-
34548065793
-
Metabolism and disposition in humans of raltegravir (MK-0518), an anti-AIDS drug targeting the HIV-1 integrase enzyme
-
Kassahun K, McIntosh I, Cui D, et al. 2007. Metabolism and disposition in humans of raltegravir (MK-0518), an anti-AIDS drug targeting the HIV-1 integrase enzyme. Drug Metab Dispos, 35:1657-63.
-
(2007)
Drug Metab Dispos
, vol.35
, pp. 1657-1663
-
-
Kassahun, K.1
McIntosh, I.2
Cui, D.3
-
17
-
-
37249040661
-
Absorption, metabolism and excretion of MK-0518, a potent HIV-1 integrase inhibitor
-
San Francisco, California, USA, Sept 27-30, abstract A-372
-
Kassahun K, McIntosh I, Hreniuk D, et al. 2006. Absorption, metabolism and excretion of MK-0518, a potent HIV-1 integrase inhibitor, in healthy male volunteers. 46th Annual Interscience Conference on Antimicrobial Agents and Chemotherapy, San Francisco, California, USA, Sept 27-30, 2006: abstract A-372.
-
(2006)
healthy male volunteers. 46th Annual Interscience Conference on Antimicrobial Agents and Chemotherapy
-
-
Kassahun, K.1
McIntosh, I.2
Hreniuk, D.3
-
18
-
-
44049090622
-
-
Kumar P, Cooper D, Steigbigel R, et al. 2007. Efficacy of raltegravir, an HIV integrase inhibitor, in combination with regimens containing enfuvirtide, darunavir, or tipranavir in patients with triple-class resistant virus: combined results from Benchmrk-1 and Benchmrk-2. European AIDS Conference. October 24-27, 2007. Madrid. Abstract P7.2/06.
-
Kumar P, Cooper D, Steigbigel R, et al. 2007. Efficacy of raltegravir, an HIV integrase inhibitor, in combination with regimens containing enfuvirtide, darunavir, or tipranavir in patients with triple-class resistant virus: combined results from Benchmrk-1 and Benchmrk-2. European AIDS Conference. October 24-27, 2007. Madrid. Abstract P7.2/06.
-
-
-
-
19
-
-
0026459411
-
Requirement of active human immunodeficiency virus type 1 integrase enzyme for productive infection of human T-lymphoid cells
-
LaFemina RL, Schneider CL, Robbins HO, et al. 1992. Requirement of active human immunodeficiency virus type 1 integrase enzyme for productive infection of human T-lymphoid cells. J Virol, 66:7414-19.
-
(1992)
J Virol
, vol.66
, pp. 7414-7419
-
-
LaFemina, R.L.1
Schneider, C.L.2
Robbins, H.O.3
-
20
-
-
33845366857
-
Antiretroviral activity, pharmacokinetics, and tolerability of MK-0518, a novel inhibitor of HIV-1 integrase, dosed as monotherapy for 10 days in treatment-naive HIV-1-infected individuals
-
Markowitz M, Morales-Ramirez JO, Nguyen BY, et al. 2006. Antiretroviral activity, pharmacokinetics, and tolerability of MK-0518, a novel inhibitor of HIV-1 integrase, dosed as monotherapy for 10 days in treatment-naive HIV-1-infected individuals. J Acquir Immune Defic Syndr, 43:509-15.
-
(2006)
J Acquir Immune Defic Syndr
, vol.43
, pp. 509-515
-
-
Markowitz, M.1
Morales-Ramirez, J.O.2
Nguyen, B.Y.3
-
21
-
-
34748860363
-
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 BY, Gotuzzo E, et al. 2007. 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, 46:125-33.
-
(2007)
J Acquir Immune Defic Syndr
, vol.46
, pp. 125-133
-
-
Markowitz, M.1
Nguyen, B.Y.2
Gotuzzo, E.3
-
22
-
-
44049089091
-
-
McColl DJ, Fransen S, Gupta S, et al. 2007. Resistance and cross-resistance to first-generation integrase inhibitors: insights from a phase II study of elvitegravir (GS-9137). Program and abstracts of the 16th International HIV Drug Resistance Workshop; June 12-16, 2007; Barbados, West Indies. Abstract 9.
-
McColl DJ, Fransen S, Gupta S, et al. 2007. Resistance and cross-resistance to first-generation integrase inhibitors: insights from a phase II study of elvitegravir (GS-9137). Program and abstracts of the 16th International HIV Drug Resistance Workshop; June 12-16, 2007; Barbados, West Indies. Abstract 9.
-
-
-
-
23
-
-
44049092298
-
-
Miller MD, Witmer MV, Stillmock KA, et al. 2006. Biochemical and antiviral activity of MK-0518, a potent HIV integrase inhibitor. In: program and abstracts of XVI International AIDS Conference; 2006, Toronto.
-
Miller MD, Witmer MV, Stillmock KA, et al. 2006. Biochemical and antiviral activity of MK-0518, a potent HIV integrase inhibitor. In: program and abstracts of XVI International AIDS Conference; 2006, Toronto.
-
-
-
-
24
-
-
34548079292
-
Atazanavir modestly increases plasma levels of MK-0518
-
Sidney, Australia, Abstract
-
Mistry G, Wenning L, Petry A, et al. 2007. Atazanavir modestly increases plasma levels of MK-0518. 4h International AIDS Society Conference on HIV Pathogenesis, Treatment and Prevention. Sidney, Australia, 2007. Abstract number:1985.
-
(2007)
4h International AIDS Society Conference on HIV Pathogenesis, Treatment and Prevention
, Issue.1985
-
-
Mistry, G.1
Wenning, L.2
Petry, A.3
-
25
-
-
0037130159
-
Structure activity of 3-aryl-1,3-diketo-containing compounds as HIV-1 integrase inhibitors
-
Pais GCG, Zhang XC, Marchand C, et al. 2002. Structure activity of 3-aryl-1,3-diketo-containing compounds as HIV-1 integrase inhibitors. J Med Chem, 45:3184-94.
-
(2002)
J Med Chem
, vol.45
, pp. 3184-3194
-
-
Pais, G.C.G.1
Zhang, X.C.2
Marchand, C.3
-
26
-
-
44049103032
-
-
Steigbigel R, Kumar P, Eron J, et al. 2007. Results of BENCHMRK-2, a phase III study evaluating the efficacy and safety of MK-0518, a novel HIV-1 integrase inhibitor, in patients with triple-class resistant virus. Program and abstracts of the 14th Conference on Retroviruses and Opportunistic Infections; February 25-28, 2007; Los Angeles, California. Abstracts 105bLB.
-
Steigbigel R, Kumar P, Eron J, et al. 2007. Results of BENCHMRK-2, a phase III study evaluating the efficacy and safety of MK-0518, a novel HIV-1 integrase inhibitor, in patients with triple-class resistant virus. Program and abstracts of the 14th Conference on Retroviruses and Opportunistic Infections; February 25-28, 2007; Los Angeles, California. Abstracts 105bLB.
-
-
-
-
27
-
-
34748822687
-
Lack of significant drug interaction between MK-0518 and tenofovir disoproxil fumarate
-
San Francisco, CA, Abstract 2006b;
-
Wenning LA, Friedman E, Kost JT, et al. 2006. Lack of significant drug interaction between MK-0518 and tenofovir disoproxil fumarate. 46th Annual ICAAC Meeting. San Francisco, CA, 2006: Abstract 2006b; A-375.
-
(2006)
46th Annual ICAAC Meeting
-
-
Wenning, L.A.1
Friedman, E.2
Kost, J.T.3
-
28
-
-
34247396153
-
Effect of tipranavir + ritonavir on pharmacokinetics of MK-0518
-
San Francisco, CA, Abstract 2006a;
-
Wenning LA, Hanley H, Stone J, et al. 2006. Effect of tipranavir + ritonavir on pharmacokinetics of MK-0518. 46th Annual ICAAC Meeting. San Francisco, CA, 2006: Abstract 2006a; A-374.
-
(2006)
46th Annual ICAAC Meeting
-
-
Wenning, L.A.1
Hanley, H.2
Stone, J.3
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