-
1
-
-
1842415431
-
Coreceptor usage of primary human immunodeficiency virus type 1 isolates varies according to biological phenotype
-
Björndal A, Deng H, Jansson M, et al. Coreceptor usage of primary human immunodeficiency virus type 1 isolates varies according to biological phenotype. J Virol. 1997;71:7478-7487.
-
(1997)
J Virol
, vol.71
, pp. 7478-7487
-
-
Björndal, A.1
Deng, H.2
Jansson, M.3
-
2
-
-
0141814730
-
The entry of entry inhibitors: A fusion of science and medicine
-
Moore JP, Doms RW. The entry of entry inhibitors: a fusion of science and medicine. Proc Natl Acad Sci U S A. 2003;100:10598-10602.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 10598-10602
-
-
Moore, J.P.1
Doms, R.W.2
-
3
-
-
10344266976
-
Primary, syncytium-inducing human immunodeficiency virus type 1 isolates are dual-tropic and most can use either Lestr or CCR5 as coreceptors for virus entry
-
Simmons G, Wilkinson D, Reeves JD, et al. Primary, syncytium-inducing human immunodeficiency virus type 1 isolates are dual-tropic and most can use either Lestr or CCR5 as coreceptors for virus entry. J Virol. 1996; 70:8355-8360.
-
(1996)
J Virol
, vol.70
, pp. 8355-8360
-
-
Simmons, G.1
Wilkinson, D.2
Reeves, J.D.3
-
4
-
-
16444381128
-
HIV type 1 phenotype, tropism, and sequence patterns: Association and preference
-
Dong XN, Chen X, Chen Y, et al. HIV type 1 phenotype, tropism, and sequence patterns: association and preference. AIDS Res Hum Retro-viruses. 2005;21:234-238.
-
(2005)
AIDS Res Hum Retro-viruses
, vol.21
, pp. 234-238
-
-
Dong, X.N.1
Chen, X.2
Chen, Y.3
-
5
-
-
0028091755
-
Macrophage-tropic variants initiate human immunodeficiency virus type 1 infection after sexual, parenteral, and vertical transmission
-
van't Wout AB, Kootstra NA, Mulder-Kampinga GA, et al. Macrophage-tropic variants initiate human immunodeficiency virus type 1 infection after sexual, parenteral, and vertical transmission. J Clin Invest. 1994;94: 2060-2067.
-
(1994)
J Clin Invest
, vol.94
, pp. 2060-2067
-
-
Van'T Wout, A.B.1
Kootstra, N.A.2
Mulder-Kampinga, G.A.3
-
6
-
-
0031575431
-
Change in coreceptor use correlates with disease progression in HIV-1-infected individuals
-
Connor RI, Sheridan KE, Ceradini D, et al. Change in coreceptor use correlates with disease progression in HIV-1-infected individuals. J Exp Med. 1997;185:621-628.
-
(1997)
J Exp Med
, vol.185
, pp. 621-628
-
-
Connor, R.I.1
Sheridan, K.E.2
Ceradini, D.3
-
7
-
-
43249097018
-
The impact of HIV tropism on decreases in CD4 cell count, clinical progression, and subsequent response to a first antiretroviral therapy regimen
-
Waters L, Mandalia S, Randell P, et al. The impact of HIV tropism on decreases in CD4 cell count, clinical progression, and subsequent response to a first antiretroviral therapy regimen. Clin Infect Dis. 2008;46: 1617-1623.
-
(2008)
Clin Infect Dis
, vol.46
, pp. 1617-1623
-
-
Waters, L.1
Mandalia, S.2
Randell, P.3
-
8
-
-
0001633495
-
Genetic restriction of HIV-1 infection and progression to AIDS by a deletion allele of the CCR5 structural gene
-
Dean M, Carrington M, Winkler C, et al. Genetic restriction of HIV-1 infection and progression to AIDS by a deletion allele of the CCR5 structural gene. Science. 1996;273:1856-1862.
-
(1996)
Science
, vol.273
, pp. 1856-1862
-
-
Dean, M.1
Carrington, M.2
Winkler, C.3
-
9
-
-
16044373004
-
Resistance to HIV-1 infection in Caucasian individuals bearing mutant alleles of the CCR-5 chemokine receptor gene
-
Samson M, Libert F, Doranz BJ, et al. Resistance to HIV-1 infection in Caucasian individuals bearing mutant alleles of the CCR-5 chemokine receptor gene. Nature. 1996;382:722-725.
-
(1996)
Nature
, vol.382
, pp. 722-725
-
-
Samson, M.1
Libert, F.2
Doranz, B.J.3
-
10
-
-
2342544143
-
Piperazine-based CCR5 antagonists as HIV-1 inhibitors. IV. Discovery of 1-[(4, 6-dimethyl-5-pyrimidinyl)carbonyl]-4-[4-[2-methoxy-1(R)-4- (trifluoromethyl)pheny-l]ethyl-3(S)-methyl-1-piperazinyl]-4-methylpiperidine (Sch-417690/Sch-D), a potent, highly selective, and orally bioavailable CCR5 antagonist
-
Tagat JR, McCombie SW, Nazareno D, et al. Piperazine-based CCR5 antagonists as HIV-1 inhibitors. IV. Discovery of 1-[(4, 6-dimethyl-5- pyrimidinyl)carbonyl]-4-[4-[2-methoxy-1(R)-4-(trifluoromethyl)pheny-l]ethyl-3(S) -methyl-1-piperazinyl]-4-methylpiperidine (Sch-417690/Sch-D), a potent, highly selective, and orally bioavailable CCR5 antagonist. J Med Chem. 2004;47:2405-2408.
-
(2004)
J Med Chem
, vol.47
, pp. 2405-2408
-
-
Tagat, J.R.1
McCombie, S.W.2
Nazareno, D.3
-
11
-
-
28944454412
-
Discovery and characterization of vicriviroc (SCH 417690), a CCR5 antagonist with potent activity against human immunodeficiency virus type 1
-
Strizki JM, Tremblay C, Xu S, et al. Discovery and characterization of vicriviroc (SCH 417690), a CCR5 antagonist with potent activity against human immunodeficiency virus type 1. Antimicrob Agents Chemother. 2005;49:4911-4919.
-
(2005)
Antimicrob Agents Chemother
, vol.49
, pp. 4911-4919
-
-
Strizki, J.M.1
Tremblay, C.2
Xu, S.3
-
12
-
-
34250006524
-
Antiviral activity, pharmacokinetics and safety of vicriviroc, an oral CCR5 antagonist, during 14-day monotherapy in HIV-infected adults
-
Schürmann D, Fätkenheuer G, Reynes J, et al. Antiviral activity, pharmacokinetics and safety of vicriviroc, an oral CCR5 antagonist, during 14-day monotherapy in HIV-infected adults. AIDS. 2007;21: 1293-1299.
-
(2007)
AIDS
, vol.21
, pp. 1293-1299
-
-
Schürmann, D.1
Fätkenheuer, G.2
Reynes, J.3
-
13
-
-
21844468794
-
Pharmacokinetics of once-daily lopinavir/ritonavir and the influence of dose modifications
-
la Porte CJ, Schippers EF, van der Ende M, et al. Pharmacokinetics of once-daily lopinavir/ritonavir and the influence of dose modifications. AIDS. 2005;19:1105-1107.
-
(2005)
AIDS
, vol.19
, pp. 1105-1107
-
-
La Porte, C.J.1
Schippers, E.F.2
Van Der Ende, M.3
-
14
-
-
34347379935
-
Phase 2 study of the safety and efficacy of vicriviroc, a CCR5 inhibitor, in HIV-1-Infected, treatment-experienced subjects: AIDS clinical trials group 5211
-
Gulick RM, Su Z, Flexner C, et al. Phase 2 study of the safety and efficacy of vicriviroc, a CCR5 inhibitor, in HIV-1-Infected, treatment-experienced subjects: AIDS clinical trials group 5211. J Infect Dis. 2007;196:304-312.
-
(2007)
J Infect Dis
, vol.196
, pp. 304-312
-
-
Gulick, R.M.1
Su, Z.2
Flexner, C.3
-
15
-
-
54749134143
-
Phase II study of vicriviroc versus efavirenz (both with zidovudine/lamivudine) in treatment-naive subjects with HIV-1 infection
-
Landovitz RJ, Angel JB, Hoffmann C, et al. Phase II study of vicriviroc versus efavirenz (both with zidovudine/lamivudine) in treatment-naive subjects with HIV-1 infection. J Infect Dis. 2008;198:1113-1122.
-
(2008)
J Infect Dis
, vol.198
, pp. 1113-1122
-
-
Landovitz, R.J.1
Angel, J.B.2
Hoffmann, C.3
-
16
-
-
0033929197
-
Population pharmacokinetics and pharmacodynamic modeling of abacavir (1592U89) from a dose-ranging, double-blind, randomized monotherapy trial with human immunodeficiency virus-infected subjects
-
Weller S, Radomski KM, Lou Y, et al. Population pharmacokinetics and pharmacodynamic modeling of abacavir (1592U89) from a dose-ranging, double-blind, randomized monotherapy trial with human immunodeficiency virus-infected subjects. Antimicrob Agents Chemother. 2000;44: 2052-2060.
-
(2000)
Antimicrob Agents Chemother
, vol.44
, pp. 2052-2060
-
-
Weller, S.1
Radomski, K.M.2
Lou, Y.3
-
17
-
-
33748113778
-
Antiviral activity, pharmacokinetics, and dose response of the HIV-1 integrase inhibitor GS-9137 (JTK-303) in treatment-naive and treatment-experienced subjects
-
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 subjects. 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
-
18
-
-
61849111053
-
Mariviroc exposure-efficacy (, 50 copies/ml) analysis in HIV 1-infected treatment näive subjects-ITT population (MERIT study)
-
July Mexico City, Mexico
-
McFadyen L, Jacqmin P, Wade J, et al. Mariviroc exposure-efficacy (, 50 copies/ml) analysis in HIV 1-infected treatment näive subjects-ITT population (MERIT study). XVII International AIDS Conference #TUPE 0053, July 2008, Mexico City, Mexico.
-
(2008)
XVII International AIDS Conference #TUPE 0053
-
-
McFadyen, L.1
Jacqmin, P.2
Wade, J.3
-
19
-
-
28144444597
-
A pharmacokinetic-pharmacody-namic disease model to predict in vivo antiviral activity of maraviroc
-
Rosario MC, Jacqmin P, Dorr P, et al. A pharmacokinetic-pharmacody-namic disease model to predict in vivo antiviral activity of maraviroc. Clin Pharmacol Ther. 2005;78:508-519.
-
(2005)
Clin Pharmacol Ther
, vol.78
, pp. 508-519
-
-
Rosario, M.C.1
Jacqmin, P.2
Dorr, P.3
-
20
-
-
59749085932
-
Weighted OBT Susceptibility Score (wOBTSS) is a stronger predictor of virologic response at 48 weeks than baseline tropism result in MOTIVATE 1 and 2
-
#H-1221; October 2008, Washington, D.C
-
Valdez H, Lewis M, Delonge C, et al. Weighted OBT Susceptibility Score (wOBTSS) is a stronger predictor of virologic response at 48 weeks than baseline tropism result in MOTIVATE 1 and 2. ICAAC, 2008, #H-1221; October 2008, Washington, D.C.
-
(2008)
ICAAC
-
-
Valdez, H.1
Lewis, M.2
Delonge, C.3
-
22
-
-
20444470810
-
Population pharmacokinetics and exposure-response relationship of enfuvirtide in treatment-experienced human immunodeficiency virus type 1-infected subjects
-
Mould DR, Zhang X, Nieforth K, et al. Population pharmacokinetics and exposure-response relationship of enfuvirtide in treatment-experienced human immunodeficiency virus type 1-infected subjects. Clin Pharmacol Ther. 2005;77:515-528.
-
(2005)
Clin Pharmacol Ther
, vol.77
, pp. 515-528
-
-
Mould, D.R.1
Zhang, X.2
Nieforth, K.3
-
23
-
-
54849146700
-
Maraviroc for previously treated subjects with R5 HIV-1 infection
-
Gulick RM, Lalezari J, Goodrich J, et al. Maraviroc for previously treated subjects with R5 HIV-1 infection. N Engl J Med. 2008;359: 1429-1441.
-
(2008)
N Engl J Med
, vol.359
, pp. 1429-1441
-
-
Gulick, R.M.1
Lalezari, J.2
Goodrich, J.3
-
24
-
-
48449104735
-
An enhanced version of the Trifle Coreceptor Tropism assay predicts emergence of CXCR4 use in ACTG5211 vicriviroc trial samples
-
# 869, Boston, MA
-
Reeves J, Han D, Wilkin T, et al. An enhanced version of the Trifle Coreceptor Tropism assay predicts emergence of CXCR4 use in ACTG5211 vicriviroc trial samples. Conference on Retroviruses and Opportunistic Infections, February, 2008, #869, Boston, MA.
-
(2008)
Conference on Retroviruses and Opportunistic Infections February
-
-
Reeves, J.1
Han, D.2
Wilkin, T.3
-
25
-
-
72949101727
-
Reanalysis of the MERIT study with the enhanced Trofile assay
-
Abstract H-1232a 25-28 October 2008, Washington, DC
-
Saag M, Heera J, Goodrich J. et al. Reanalysis of the MERIT study with the enhanced Trofile assay. Abstract H-1232a. 48th ICAAC, 25-28 October 2008, Washington, DC.
-
48th ICAAC
-
-
Saag, M.1
Heera, J.2
Goodrich, J.3
-
26
-
-
70350179577
-
Response to vicriviroc in treatment-experienced subjects using an enhanced sensitivity co-receptor tropism assay: Reanalysis of AIDS Clinical Trials Group A5211
-
Su Z, Gulick R, Krambrink A. Response to vicriviroc in treatment-experienced subjects using an enhanced sensitivity co-receptor tropism assay: reanalysis of AIDS Clinical Trials Group A5211. J Infect Dis. 2009, 200:1724-1728.
-
(2009)
J Infect Dis
, vol.200
, pp. 1724-1728
-
-
Su, Z.1
Gulick, R.2
Krambrink, A.3
-
27
-
-
33847237614
-
Reduced maximal inhibition in phenotypic susceptibility assays indicates that viral strains resistant to the CCR5 antagonist maraviroc utilize inhibitor-bound receptor for entry
-
Westby M, Smith-Burchnell C, Mori J, et al. Reduced maximal inhibition in phenotypic susceptibility assays indicates that viral strains resistant to the CCR5 antagonist maraviroc utilize inhibitor-bound receptor for entry. J Virol. 2007;81:2359-2371.
-
(2007)
J Virol
, vol.81
, pp. 2359-2371
-
-
Westby, M.1
Smith-Burchnell, C.2
Mori, J.3
-
28
-
-
40849085150
-
Mapping resistance to the CCR5 co-receptor antagonist vicriviroc using heterologous chimeric HIV-1 envelope genes reveals key determinants in the C2-V5 domain of gp120
-
Ogert RA, Wojcik L, Buontempo C, et al. Mapping resistance to the CCR5 co-receptor antagonist vicriviroc using heterologous chimeric HIV-1 envelope genes reveals key determinants in the C2-V5 domain of gp120. Virology. 2008;373:387-399.
-
(2008)
Virology
, vol.373
, pp. 387-399
-
-
Ogert, R.A.1
Wojcik, L.2
Buontempo, C.3
-
29
-
-
49149118151
-
In vivo emergence of vicriviroc resistance in a human immunodeficiency virus type 1 subtype C-infected subject
-
Tsibris AM, Sagar M, Gulick RM, et al., In vivo emergence of vicriviroc resistance in a human immunodeficiency virus type 1 subtype C-infected subject. J Virol. 2008;82:8210-8214.
-
(2008)
J Virol
, vol.82
, pp. 8210-8214
-
-
Tsibris, A.M.1
Sagar, M.2
Gulick, R.M.3
-
30
-
-
40849098660
-
Molecular interactions of CCR5 with major classes of small-molecule anti-HIV CCR5 antagonists
-
Kondru R, Zhang J, Ji C, et al. Molecular interactions of CCR5 with major classes of small-molecule anti-HIV CCR5 antagonists. Mol Pharmacol. 2008;73:789-800.
-
(2008)
Mol Pharmacol
, vol.73
, pp. 789-800
-
-
Kondru, R.1
Zhang, J.2
Ji, C.3
-
31
-
-
28544434492
-
CCR5 antagonists: Host-targeted antivirals for the treatment of HIV infection
-
Westby M, van der Ryst E. CCR5 antagonists: host-targeted antivirals for the treatment of HIV infection. Antivir Chem Chemother. 2005;16: 339-354.
-
(2005)
Antivir Chem Chemother
, vol.16
, pp. 339-354
-
-
Westby, M.1
Van Der Ryst, E.2
-
32
-
-
36348955045
-
Liver cytochrome P450 enzymes involved in biotransformation of vicriviroc, a CCR5 receptor antagonist
-
Ghosal A, Ramanathan R, Yuan Y, et al. Liver cytochrome P450 enzymes involved in biotransformation of vicriviroc, a CCR5 receptor antagonist. Drug Metab Dispos. 2007;35:2186-2195.
-
(2007)
Drug Metab Dispos
, vol.35
, pp. 2186-2195
-
-
Ghosal, A.1
Ramanathan, R.2
Yuan, Y.3
-
33
-
-
34249980945
-
Pharmacokinetics of vicriviroc are not affected in combination with five different protease inhibitors boosted by ritonavir.
-
Program and abstracts of the Denver, CO, February 5-8 Abstract 582
-
Sansone A, Keung A, Tetteh E, et al. Pharmacokinetics of vicriviroc are not affected in combination with five different protease inhibitors boosted by ritonavir. Program and abstracts of the 13th Conference on Retroviruses and Opportunistic Infections. Denver, CO, February 5-8, 2006. Abstract 582.
-
(2006)
13th Conference on Retroviruses and Opportunistic Infections
-
-
Sansone, A.1
Keung, A.2
Tetteh, E.3
-
34
-
-
77950263227
-
Effect of food on bioavailability of SCH 4 17690 in healthy volunteers
-
Washington, DC, December 16-19 Washington, DC. Abstract A-1200
-
Sansone A, Keung A, Caceres M, et al. Effect of food on bioavailability of SCH 4 17690 in healthy volunteers. Programs and abstracts of the 45th Interscience Conference on Antimicrobial Agents and Chemotherapy, Washington, DC, December 16-19, 2005, Washington, DC. Abstract A-1200.
-
(2005)
Programs and Abstracts of the 45th Interscience Conference on Antimicrobial Agents and Chemotherapy
-
-
Sansone, A.1
Keung, A.2
Caceres, M.3
-
35
-
-
57749197592
-
Dose-response of ritonavir on hepatic CYP3A activity and elvitegravir oral exposure
-
Mathias AA, West S, Hui J, et al. 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
-
36
-
-
52149101363
-
Vicriviroc, a next generation CCR5 antagonist, exhibits potent, sustained suppression of viral replication in treatment-experienced adults: VICTOR-E1 48-week results
-
# 39L, Boston, MA
-
Zingman B, Suleiman J, DeJesus E, et al. Vicriviroc, a next generation CCR5 antagonist, exhibits potent, sustained suppression of viral replication in treatment-experienced adults: VICTOR-E1 48-week results. Conference on Retroviruses and Opportunistic Infections, 2008, #39L, Boston, MA
-
(2008)
Conference on Retroviruses and Opportunistic Infections
-
-
Zingman, B.1
Suleiman, J.2
Dejesus, E.3
|