-
1
-
-
0037249691
-
Long-term HIV/AIDS survival estimation in the highly active antiretroviral therapy era
-
King, J. T. Jr et al. Long-term HIV/AIDS survival estimation in the highly active antiretroviral therapy era. Med. Decis. Making 23, 9-20 (2003).
-
(2003)
Med. Decis. Making
, vol.23
, pp. 9-20
-
-
King Jr., J.T.1
-
2
-
-
0035882308
-
Initial virological and immunologic response to highly active antiretroviral therapy predicts long-term clinical outcome
-
Kitchen, C. M. et al. Initial virological and immunologic response to highly active antiretroviral therapy predicts long-term clinical outcome. Clin. Infect. Dis. 33, 466-472 (2001).
-
(2001)
Clin. Infect. Dis.
, vol.33
, pp. 466-472
-
-
Kitchen, C.M.1
-
3
-
-
0034977285
-
HAART is cost-effective and improves outcomes
-
Valenti, W. M. HAART is cost-effective and improves outcomes. AIDS Read. 11, 260-262 (2001).
-
(2001)
AIDS Read.
, vol.11
, pp. 260-262
-
-
Valenti, W.M.1
-
5
-
-
0037043652
-
Antiretroviral-drug resistance among patients recently infected with HIV
-
Little, S. E. et al. Antiretroviral-drug resistance among patients recently infected with HIV. N. Engl. J. Med. 347, 385-394 (2002).
-
(2002)
N. Engl. J. Med.
, vol.347
, pp. 385-394
-
-
Little, S.E.1
-
6
-
-
1342338945
-
HIV drug resistance: Implications for management
-
Hammer, S. M. HIV drug resistance: Implications for management. Top. HIV Med. 10, 10-15 (2002).
-
(2002)
Top. HIV Med.
, vol.10
, pp. 10-15
-
-
Hammer, S.M.1
-
7
-
-
0344559097
-
Current management challenges in HIV: Antiretroviral resistance
-
Kuritzkes, D. R. et al. Current management challenges in HIV: antiretroviral resistance. AIDS Pead. 13, 133-142 (2003).
-
(2003)
AIDS Pead.
, vol.13
, pp. 133-142
-
-
Kuritzkes, D.R.1
-
8
-
-
0035833384
-
Antiretroviral therapy for previously treated patients
-
Montaner, J. S. & Mellors, J. W. Antiretroviral therapy for previously treated patients. N. Engl. J. Med. 345, 452-455 (2001).
-
(2001)
N. Engl. J. Med.
, vol.345
, pp. 452-455
-
-
Montaner, J.S.1
Mellors, J.W.2
-
9
-
-
0035912249
-
HIV chemotherapy
-
Richman, D. D. HIV chemotherapy. Nature 410, 995-1001 (2001).
-
(2001)
Nature
, vol.410
, pp. 995-1001
-
-
Richman, D.D.1
-
10
-
-
0034924823
-
Mechanisms of viral membrane fusion and its inhibition
-
Eckert, D. M. & Kim, P. S. Mechanisms of viral membrane fusion and its inhibition. Annu. Rev. Biochem. 70, 777-810 (2001).
-
(2001)
Annu. Rev. Biochem.
, vol.70
, pp. 777-810
-
-
Eckert, D.M.1
Kim, P.S.2
-
11
-
-
0035036358
-
HIV fusion and its inhibition
-
LaBranche, C. C. et al. HIV fusion and its inhibition. Antiviral Res. 60, 95-115 (2001).
-
(2001)
Antiviral Res.
, vol.60
, pp. 95-115
-
-
LaBranche, C.C.1
-
12
-
-
0024237197
-
Oligomeric structure of a prototype retrovirus glycoprotein
-
Einfeld, D. & Hunter, E. Oligomeric structure of a prototype retrovirus glycoprotein. Proc. Natl Acad. Sci. USA 85, 8688-8692 (1988).
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 8688-8692
-
-
Einfeld, D.1
Hunter, E.2
-
13
-
-
0024327732
-
Oligomeric structure of gp41, the transmembrane protein of human immunodeficiency virus type 1
-
Pinter, A. et al. Oligomeric structure of gp41, the transmembrane protein of human immunodeficiency virus type 1. J. Virol. 63, 2674-2679 (1989).
-
(1989)
J. Virol.
, vol.63
, pp. 2674-2679
-
-
Pinter, A.1
-
14
-
-
0032546844
-
The HIV-1 envelope glycoproteins: Fusogens, antigens, and immunogens
-
Wyatt, R. & Sodroski, J. The HIV-1 envelope glycoproteins: fusogens, antigens, and immunogens. Science 280, 1884-1888 (1998).
-
(1998)
Science
, vol.280
, pp. 1884-1888
-
-
Wyatt, R.1
Sodroski, J.2
-
15
-
-
0038065763
-
Dilation of the human immunodeficiency virus-1 envelope glycoprotein fusion pore revealed by the inhibitory action of a synthetic peptide from gp41
-
Munoz-Barroso, I. et al. Dilation of the human immunodeficiency virus-1 envelope glycoprotein fusion pore revealed by the inhibitory action of a synthetic peptide from gp41. J. Cell. Biol. 140, 315-323 (1998).
-
(1998)
J. Cell Biol.
, vol.140
, pp. 315-323
-
-
Munoz-Barroso, I.1
-
16
-
-
0028168944
-
Structural rearrangements in the transmembrane glycoprotein after receptor binding
-
Matthews, T. J. et al. Structural rearrangements in the transmembrane glycoprotein after receptor binding. Immunol. Rev. 140, 93-104 (1994).
-
(1994)
Immunol. Rev.
, vol.140
, pp. 93-104
-
-
Matthews, T.J.1
-
17
-
-
0026465468
-
A synthetic peptide inhibitor of human immunodeficiency virus replication: Correlation between solution structure and viral inhibition
-
Wild, C. et al. A synthetic peptide inhibitor of human immunodeficiency virus replication: Correlation between solution structure and viral inhibition. Proc. Natl Acad. Sci. USA 89, 10537-10541 (1992).
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 10537-10541
-
-
Wild, C.1
-
18
-
-
0028575843
-
Propensity for a leucine zipper-like domain of human immunodeficiency virus type 1 gp41 to form oligomers correlates with a role in virus-induced fusion rather than assembly of the glycoprotein complex
-
Wild, C. et al. Propensity for a leucine zipper-like domain of human immunodeficiency virus type 1 gp41 to form oligomers correlates with a role in virus-induced fusion rather than assembly of the glycoprotein complex. Proc. Natl Acad. Sci. USA 91, 12676-12680 (1994).
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 12676-12680
-
-
Wild, C.1
-
19
-
-
0027692502
-
A synthetic peptide from HIV-1 gp41 is a potent inhibitor of virus-mediated cell-cell fusion
-
Wild, C., Greenwell, T. & Matthews T. A synthetic peptide from HIV-1 gp41 is a potent inhibitor of virus-mediated cell-cell fusion. AIDS Res. Hum. Retroviruses 9, 1051-1053 (1993).
-
(1993)
AIDS Res. Hum. Retroviruses
, vol.9
, pp. 1051-1053
-
-
Wild, C.1
Greenwell, T.2
Matthews, T.3
-
20
-
-
0027959493
-
Peptides corresponding to a predictive α-helical domain of human immunodeficiency virus type 1 gp41 are potent inhibitors of virus infection
-
Wild, C. T. et al. Peptides corresponding to a predictive α-helical domain of human immunodeficiency virus type 1 gp41 are potent inhibitors of virus infection. Proc. Natl Acad. Sci. USA 91, 9770-9774 (1994).
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 9770-9774
-
-
Wild, C.T.1
-
21
-
-
0029072191
-
A molecular clasp in the human immunodeficiency virus (HIV) type 1 TM protein determines the anti-HIV activity of gp41 derivatives: Implication for viral fusion
-
Chen, C. H. et al. A molecular clasp in the human immunodeficiency virus (HIV) type 1 TM protein determines the anti-HIV activity of gp41 derivatives: Implication for viral fusion. J. Virol. 69, 3771-3777 (1995).
-
(1995)
J. Virol.
, vol.69
, pp. 3771-3777
-
-
Chen, C.H.1
-
22
-
-
0035846960
-
Mode of action of an antiviral peptide from HIV-1
-
Kliger, Y. et al. Mode of action of an antiviral peptide from HIV-1. J. Biol. Chem. 276, 1391-1397 (2001).
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 1391-1397
-
-
Kliger, Y.1
-
23
-
-
0031729823
-
Potent suppression of HIV-1 replication in humans by T-20, a peptide inhibitor of gp41-mediated virus entry
-
Kilby, J. M. et al. Potent suppression of HIV-1 replication in humans by T-20, a peptide inhibitor of gp41-mediated virus entry. Nature Med. 4, 1302-1307 (1998).
-
(1998)
Nature Med.
, vol.4
, pp. 1302-1307
-
-
Kilby, J.M.1
-
24
-
-
0036066762
-
The safety plasma pharmacokinetics, and antiviral activity of subcutaneous enfuvirtide (T-20), a peptide inhibitor of gp41-mediated virus fusion, in HIV-infected adults
-
Kilby, J. M. et al. The safety plasma pharmacokinetics, and antiviral activity of subcutaneous enfuvirtide (T-20), a peptide inhibitor of gp41-mediated virus fusion, in HIV-infected adults. AIDS Res. Hum. Retroviruses 18, 685-693 (2002).
-
(2002)
AIDS Res. Hum. Retroviruses
, vol.18
, pp. 685-693
-
-
Kilby, J.M.1
-
25
-
-
1642366019
-
Subgroup analysis of baseline (BL) susceptibility and early virological response to enfuvirtide in the combined TORO studies
-
Sista, P. et al. Subgroup analysis of baseline (BL) susceptibility and early virological response to enfuvirtide in the combined TORO studies. Antivir. Ther. 8, S60 (2003).
-
(2003)
Antivir. Ther.
, vol.8
-
-
Sista, P.1
-
26
-
-
0037471311
-
A phase II clinical study of the long-term safety and antiviral activity of enfuvirtide-based antiretroviral therapy
-
Lalezari, J. P. et al. A phase II clinical study of the long-term safety and antiviral activity of enfuvirtide-based antiretroviral therapy. AIDS 17, 691-698 (2003).
-
(2003)
AIDS
, vol.17
, pp. 691-698
-
-
Lalezari, J.P.1
-
27
-
-
10744229122
-
A controlled Phase II trial assessing three doses of enfuvirtide (T-20) in combination with abacavir, amprenavir, ritonavir and efavirenz in non-nucleoside reverse transcriptase inhibitor-naive HIV-infected adults
-
Lalezari, J. P. et al. A controlled Phase II trial assessing three doses of enfuvirtide (T-20) in combination with abacavir, amprenavir, ritonavir and efavirenz in non-nucleoside reverse transcriptase inhibitor-naive HIV-infected adults. Antivir. Ther. 8, 279-287 (2003).
-
(2003)
Antivir. Ther.
, vol.8
, pp. 279-287
-
-
Lalezari, J.P.1
-
28
-
-
2342614844
-
Safety, tolerability and plasma pharmacokinetics of high-strength formulations of enfuvirtide (T-20) in treatment-experienced HIV-1-infected patients
-
(in the press)
-
Wheeler, D. A. et al. Safety, tolerability and plasma pharmacokinetics of high-strength formulations of enfuvirtide (T-20) in treatment-experienced HIV-1-infected patients. J. Clin. Virol. (in the press).
-
J. Clin. Virol.
-
-
Wheeler, D.A.1
-
29
-
-
0011581041
-
Tolerability of enfuvirtide (T-20) during chronic therapy in Phase II trials
-
A H-171
-
Drobnes, C. et al. Tolerability of enfuvirtide (T-20) during chronic therapy in Phase II trials. 42nd Intersci. Conf. Antimicrob. Agents Chemother. A H-171 (2002).
-
(2002)
42nd Intersci. Conf. Antimicrob. Agents Chemother.
-
-
Drobnes, C.1
-
30
-
-
0042885473
-
Influence of subcutaneous injection site on the steady state pharmacokinetics of enfuvirtide (T-20) in HIV-1-infected patients
-
Lalezari, J. P. et al. Influence of subcutaneous injection site on the steady state pharmacokinetics of enfuvirtide (T-20) in HIV-1-infected patients. J. Clin. Virol. 28, 217-222 (2003).
-
(2003)
J. Clin. Virol.
, vol.28
, pp. 217-222
-
-
Lalezari, J.P.1
-
31
-
-
0036335809
-
Pharmacokinetics of plasma enfuvirtide after subcutaneous administration to patients with human immunodeficiency virus: Inverse Gaussian density absorption and 2-compartment disposition
-
Zhang, X. et al. Pharmacokinetics of plasma enfuvirtide after subcutaneous administration to patients with human immunodeficiency virus: Inverse Gaussian density absorption and 2-compartment disposition. Clin. Pharmacol. Ther. 72, 10-19 (2002).
-
(2002)
Clin. Pharmacol. Ther.
, vol.72
, pp. 10-19
-
-
Zhang, X.1
-
32
-
-
0347386386
-
Assessment of metabolic inhibition potential of enfuvirtide using a 5-drug cocktail in HIV-1 infected patients
-
A PIII-73
-
Zhang, X. et al. Assessment of metabolic inhibition potential of enfuvirtide using a 5-drug cocktail in HIV-1 infected patients. Am. Soc. Clin. Pharmacol. Ther. A PIII-73 (2003).
-
(2003)
Am. Soc. Clin. Pharmacol. Ther.
-
-
Zhang, X.1
-
33
-
-
0141451457
-
Enfuvirtide - Investigations on the drug interaction potential in HIV-infected patients
-
Boyd, M. et al. Enfuvirtide - investigations on the drug interaction potential in HIV-infected patients. 10th Conf. Retrovir. Opportunistic Infect. A541 (2003).
-
(2003)
10th Conf. Retrovir. Opportunistic Infect.
-
-
Boyd, M.1
-
34
-
-
1642292791
-
Enfuvirtide pharmacokinetic-pharmacodynamic (PK-PD) relationship
-
A4.1/4
-
Zhang, X. et al. Enfuvirtide pharmacokinetic-pharmacodynamic (PK-PD) relationship. 9th Eur. AIDS Conf. A4.1/4 (2003).
-
(2003)
9th Eur. AIDS Conf.
-
-
Zhang, X.1
-
35
-
-
0038576281
-
Enfuvirtide, an HIV-1 fusion inhibitor, for drug-resistant HIV infection in North and South America
-
Lalezari, J. P. et al. Enfuvirtide, an HIV-1 fusion inhibitor, for drug-resistant HIV infection in North and South America. N. Engl. J. Med. 348, 2175-2185 (2003).
-
(2003)
N. Engl. J. Med.
, vol.348
, pp. 2175-2185
-
-
Lalezari, J.P.1
-
36
-
-
0037849954
-
Efficacy of enfuvirtide in patients infected with drug-resistant HIV-1 in Europe and Australia
-
Lazzarin, A. et al. Efficacy of enfuvirtide in patients infected with drug-resistant HIV-1 in Europe and Australia. N. Engl. J. Med. 348, 2186-2195 (2003).
-
(2003)
N. Engl. J. Med.
, vol.348
, pp. 2186-2195
-
-
Lazzarin, A.1
-
37
-
-
0037877259
-
Summary of pooled efficacy and safety analyses of enfuvirtide (ENF) treatment for 24 weeks in TORO 1 and TORO 2 Phase III trials in highly antiretroviral (ARV) treatment-experienced patients
-
Delfraissy, J. F. et al. Summary of pooled efficacy and safety analyses of enfuvirtide (ENF) treatment for 24 weeks in TORO 1 and TORO 2 Phase III trials in highly antiretroviral (ARV) treatment-experienced patients. 10th Conf. Retrovir. Opportunistic Infect. A568 (2003).
-
(2003)
10th Conf. Retrovir. Opportunistic Infect.
-
-
Delfraissy, J.F.1
-
38
-
-
0242705329
-
Enfuvirtide TORO studies: 48 week results confirm 24 week findings
-
A LB2
-
Katlama, C. et al. Enfuvirtide TORO studies: 48 week results confirm 24 week findings. 2nd Int. AIDS Soc. Conf. HIV Pathog. Treat. A LB2 (2003).
-
(2003)
2nd Int. AIDS Soc. Conf. HIV Pathog. Treat.
-
-
Katlama, C.1
-
39
-
-
1642310750
-
Durability of response of enfuvirtide through 48 weeks in the TORO trials
-
A H-835
-
Trottier, B. et al. Durability of response of enfuvirtide through 48 weeks in the TORO trials. 43rd Intersci. Conf. Antimicrob. Agents Chemother. A H-835 (2003).
-
(2003)
43rd Intersci. Conf. Antimicrob. Agents Chemother.
-
-
Trottier, B.1
-
40
-
-
1642314025
-
Efficacy of enfuvirtide in subgroups of patients through 48 weeks of therapy in the TORO trials
-
A7.3/15
-
Walmsley, S. et al. Efficacy of enfuvirtide in subgroups of patients through 48 weeks of therapy in the TORO trials. 9th Eur. AIDS Conf. A7.3/15 (2003).
-
(2003)
9th Eur. AIDS Conf.
-
-
Walmsley, S.1
-
41
-
-
0012013998
-
Enfuvirtide (T-20) in combination with an optimized background (OB) regimen vs. OB alone: Week 24 response among categories of treatment experience and baseline (BL) HIV antiretroviral (ARV) resistance
-
Lalezari, J. et al. Enfuvirtide (T-20) in combination with an optimized background (OB) regimen vs. OB alone: Week 24 response among categories of treatment experience and baseline (BL) HIV antiretroviral (ARV) resistance. 42nd Intersci. Conf. Antimicrob. Agents Chemother. A3232 (2002).
-
(2002)
42nd Intersci. Conf. Antimicrob. Agents Chemother.
-
-
Lalezari, J.1
-
42
-
-
0141954433
-
Enfuvirtide (T-20) in combination with an optimized background (OB) regimen vs. OB alone: Week 24 response among categories of treatment experience and baseline (BL) demographics, treatment experience and HIV anti-retroviral (ARV) resistance
-
A PL14.3
-
Lange, J. et al. Enfuvirtide (T-20) in combination with an optimized background (OB) regimen vs. OB alone: Week 24 response among categories of treatment experience and baseline (BL) demographics, treatment experience and HIV anti-retroviral (ARV) resistance. 6th Int. Congress Drug Ther. HIV Infect. A PL14.3 (2002).
-
(2002)
6th Int. Congress Drug Ther. HIV Infect.
-
-
Lange, J.1
-
43
-
-
1642357851
-
Analysis of virological response to enfuvirtide in TORO: Implications for patient management
-
Montaner, J. et al. Analysis of virological response to enfuvirtide in TORO: Implications for patient management. 2nd Intern AIDS Soc. Conf. HIV Pathog. Treat. A116 (2003).
-
(2003)
2nd Intern AIDS Soc. Conf. HIV Pathog. Treat.
-
-
Montaner, J.1
-
44
-
-
25744441277
-
Analysis of virological failure through 24 weeks of treatment in the TORO pivotal studies
-
Battegay, M. et al. Analysis of virological failure through 24 weeks of treatment in the TORO pivotal studies. 2nd Int. AIDS Soc. Conf. HIV Pathog. Treat. A574 (2003).
-
(2003)
2nd Int. AIDS Soc. Conf. HIV Pathog. Treat.
-
-
Battegay, M.1
-
45
-
-
0031883832
-
Determinants of human immunodeficiency virus type 1 resistance to gp41-derived inhibitory peptides
-
Rimsky L. T., Shugars, D. C. & Matthews, T. J. Determinants of human immunodeficiency virus type 1 resistance to gp41-derived inhibitory peptides. J. Virol. 72, 986-993 (1998).
-
(1998)
J. Virol.
, vol.72
, pp. 986-993
-
-
Rimsky, L.T.1
Shugars, D.C.2
Matthews, T.J.3
-
46
-
-
0030970693
-
Core structure of gp41 from the HIV envelope glycoprotein
-
Chan, D. C. et al. Core structure of gp41 from the HIV envelope glycoprotein. Cell 89, 263-273 (1997).
-
(1997)
Cell
, vol.89
, pp. 263-273
-
-
Chan, D.C.1
-
47
-
-
0030962291
-
Atomic structure of the ectodomain from HIV-1 gp41
-
Weissenhorn, W. et al. Atomic structure of the ectodomain from HIV-1 gp41. Nature 387, 426-430 (1997).
-
(1997)
Nature
, vol.387
, pp. 426-430
-
-
Weissenhorn, W.1
-
48
-
-
0006918544
-
HIV-1 selection in response to inhibition of virus fusion and entry
-
Wei, X. et al. HIV-1 selection in response to inhibition of virus fusion and entry. 6th Conf. Retrovir. Opportunistic Infect. A611 (1999).
-
(1999)
6th Conf. Retrovir. Opportunistic Infect.
-
-
Wei, X.1
-
49
-
-
0038069784
-
Impact of HIV-1 gp41 amino acid substitutions (positions 36-45) on susceptibility of T-20 (enfuvirtide) in vitro: Analysis of primary virus isolates recovered from patients during chronic enfuvirtide treatment and site-directed mutants in NL4-3
-
Mink, M. et al. Impact of HIV-1 gp41 amino acid substitutions (positions 36-45) on susceptibility of T-20 (enfuvirtide) in vitro: analysis of primary virus isolates recovered from patients during chronic enfuvirtide treatment and site-directed mutants in NL4-3. Antivir. Ther. 7, S24 (2002).
-
(2002)
Antivir. Ther.
, vol.7
-
-
Mink, M.1
-
50
-
-
1642294438
-
Correlation of gp41 binding and antiviral potencies of the T-20 fusion inhibitor using clinical trial isolate-derived sequences
-
Mink, M. A. et al. Correlation of gp41 binding and antiviral potencies of the T-20 fusion inhibitor using clinical trial isolate-derived sequences. 8th Conf. Retrovir. Opportunistic Infect. A474 (2001).
-
(2001)
8th Conf. Retrovir. Opportunistic Infect.
-
-
Mink, M.A.1
-
51
-
-
0012885271
-
Characterization of baseline and treatment-emergent resistance to T-20 (enfuvirtide) observed in Phase II trials: Substitutions in gp41 amino acids 36-45 and enfuvirtide susceptibility of virus isolates
-
Sista, P. et al. Characterization of baseline and treatment-emergent resistance to T-20 (enfuvirtide) observed in Phase II trials: Substitutions in gp41 amino acids 36-45 and enfuvirtide susceptibility of virus isolates. Antivir. Ther. 7, S16 (2002).
-
(2002)
Antivir. Ther.
, vol.7
-
-
Sista, P.1
-
52
-
-
25744452785
-
Impaired fitness of human immunodeficiency virus type 1 site-directed mutants resistant to T-20
-
Lu, J. & Kuritzkes, D. R. Impaired fitness of human immunodeficiency virus type 1 site-directed mutants resistant to T-20. 5th Int. Workshop HIV Drug Resist. Treat. Strateg. A23 (2001).
-
(2001)
5th Int. Workshop HIV Drug Resist. Treat. Strateg.
-
-
Lu, J.1
Kuritzkes, D.R.2
-
53
-
-
0037539498
-
Fitness of HIV-1 clinical isolates resistant to T-20 (enfuvirtide)
-
Lu, J. et al. Fitness of HIV-1 clinical isolates resistant to T-20 (enfuvirtide). Antivir. Ther. 7, S74 (2002).
-
(2002)
Antivir. Ther.
, vol.7
-
-
Lu, J.1
-
54
-
-
0034890660
-
Sensitivity of human immunodeficiency virus type 1 to fusion inhibitors targeted to the gp41 first heptad repeat involves district regions of gp41 and is consistently modulated by gp120 interactions with the coreceptor
-
Derdeyn, C. A. et al. Sensitivity of human immunodeficiency virus type 1 to fusion inhibitors targeted to the gp41 first heptad repeat involves district regions of gp41 and is consistently modulated by gp120 interactions with the coreceptor. J. Virol. 75, 8605-8614 (2001).
-
(2001)
J. Virol.
, vol.75
, pp. 8605-8614
-
-
Derdeyn, C.A.1
-
55
-
-
0009833551
-
Sensitivity of HIV-1 to the fusion inhibitors T-20 and T-649 is modulated by coreceptor specificity and involves distinct regions of gp41
-
Derdeyn, C. A. et al. Sensitivity of HIV-1 to the fusion inhibitors T-20 and T-649 is modulated by coreceptor specificity and involves distinct regions of gp41. 8th Conf. Retrovir. Opportunistic Infect. A475 (2001).
-
(2001)
8th Conf. Retrovir. Opportunistic Infect.
-
-
Derdeyn, C.A.1
-
56
-
-
0003339453
-
SCH C: Safety and antiviral effects of a CCR5 receptor antagonist in HIV-1 infected subjects
-
Reynes, J. et al. SCH C: Safety and antiviral effects of a CCR5 receptor antagonist in HIV-1 infected subjects. 9th Conf. Retrovir. Opportunistic Infect. A1 (2002).
-
(2002)
9th Conf. Retrovir. Opportunistic Infect.
-
-
Reynes, J.1
-
57
-
-
0010459359
-
Virus sensitivity to T-20 and T-1249 is independent of coreceptor usage
-
Greenberg, M. L. et al. Virus sensitivity to T-20 and T-1249 is independent of coreceptor usage. 8th Conf. Retrovir. Opportunistic Infect. A473 (2001).
-
(2001)
8th Conf. Retrovir. Opportunistic Infect.
-
-
Greenberg, M.L.1
-
58
-
-
0042895999
-
Analysis of baseline enfuvirtide (T20) susceptibility and co-receptor tropism in two Phase III study populations
-
Whitcomb, J. M. et al. Analysis of baseline enfuvirtide (T20) susceptibility and co-receptor tropism in two Phase III study populations. 10th Conf. Retrovir. Opportunistic Infect. A557 (2003).
-
(2003)
10th Conf. Retrovir. Opportunistic Infect.
-
-
Whitcomb, J.M.1
-
59
-
-
0012823617
-
Baseline and on-treatment susceptibility to enfuvirtide seen in TORO 1 and TORO 2 through 24 weeks
-
Greenberg, M. et al. Baseline and on-treatment susceptibility to enfuvirtide seen in TORO 1 and TORO 2 through 24 weeks. 10th Conf. Retrovir. Opportunistic Infect. A141 (2003).
-
(2003)
10th Conf. Retrovir. Opportunistic Infect.
-
-
Greenberg, M.1
-
60
-
-
1642414599
-
Safety of enfuvirtide (ENF) through 48 weeks of therapy in the TORO trials
-
A H-836
-
Eron, J. et al. Safety of enfuvirtide (ENF) through 48 weeks of therapy in the TORO trials. 43rd Intersci. Conf. Antimicrob. Agents Chemother. A H-836 (2003).
-
(2003)
43rd Intersci. Conf. Antimicrob. Agents Chemother.
-
-
Eron, J.1
-
61
-
-
0142244854
-
Injection site reactions with the HIV-1 fusion inhibitor enfuvirtide
-
Ball, R. A. & Kinchelow, T. Injection site reactions with the HIV-1 fusion inhibitor enfuvirtide. J. Am. Acad. Dermatol. 49, 826-831 (2003).
-
(2003)
J. Am. Acad. Dermatol.
, vol.49
, pp. 826-831
-
-
Ball, R.A.1
Kinchelow, T.2
-
62
-
-
9144264190
-
Enfuvirtide (T-20) cross-reactive gp41 antibody has no effect on the efficacy or safety of enfuvirtide in the TORO 1 and TORO 2 Phase III trials
-
Walmsley, S. et al. Enfuvirtide (T-20) cross-reactive gp41 antibody has no effect on the efficacy or safety of enfuvirtide in the TORO 1 and TORO 2 Phase III trials. J. Infect. Dis. 188, 1827-1833 (2003).
-
(2003)
J. Infect. Dis.
, vol.188
, pp. 1827-1833
-
-
Walmsley, S.1
-
63
-
-
0142186214
-
Patient acceptance of self-injected enfuvirtide at 8 and 24 weeks
-
Cohen, C. et al. Patient acceptance of self-injected enfuvirtide at 8 and 24 weeks. HIV Clin. Trials 4, 347-357 (2003).
-
(2003)
HIV Clin. Trials
, vol.4
, pp. 347-357
-
-
Cohen, C.1
-
64
-
-
0348230772
-
Patient acceptance with self-injection of enfuvirtide (ENF) for HIV over 48 weeks of treatment
-
A7.1/1
-
Cohen, C. et al. Patient acceptance with self-injection of enfuvirtide (ENF) for HIV over 48 weeks of treatment. 9th Eur. AIDS Conf. A7.1/1 (2003).
-
(2003)
9th Eur. AIDS Conf.
-
-
Cohen, C.1
-
65
-
-
0347600772
-
Impact of enfuvirtide on health-related quality of life at 48 weeks
-
A 7.3/19
-
Clumeck, N. et al. Impact of enfuvirtide on health-related quality of life at 48 weeks. 9th Eur. AIDS Conf. A 7.3/19 (2003).
-
(2003)
9th Eur. AIDS Conf.
-
-
Clumeck, N.1
-
66
-
-
0038187684
-
Novel therapies based on mechanisms of HIV-1 cell entry
-
Kilby, J. M. & Eron, J. J. Novel therapies based on mechanisms of HIV-1 cell entry N. Engl. J. Med. 348, 2228-2238 (2003).
-
(2003)
N. Engl. J. Med.
, vol.348
, pp. 2228-2238
-
-
Kilby, J.M.1
Eron, J.J.2
-
67
-
-
0003309527
-
Identification and characterization of a novel inhibitor of HIV-1 entry - II: Mechanism of action
-
Lin, P. F. et al. Identification and characterization of a novel inhibitor of HIV-1 entry - II: Mechanism of action. 9th Conf. Retrovir. Opportunistic Infect. A10 (2002).
-
(2002)
9th Conf. Retrovir. Opportunistic Infect.
-
-
Lin, P.F.1
-
68
-
-
0038022225
-
Safety and preliminary anti-HIV activity of an anti-CD4 mAb (TNX-355; formerly Hu5A8) in HIV-infected patients
-
Kuritzkes, D. R. et al. Safety and preliminary anti-HIV activity of an anti-CD4 mAb (TNX-355; formerly Hu5A8) in HIV-infected patients. 10th Conf. Retrovir. Opportunistic Infect. A13 (2003).
-
(2003)
10th Conf. Retrovir. Opportunistic Infect.
-
-
Kuritzkes, D.R.1
-
69
-
-
1642411357
-
PRO 542 (CD4-IgG2) has a profound impact on HIV-1 replication in the Hu-PBL-SCID mouse model
-
A410-T
-
Franti, M. et al. PRO 542 (CD4-IgG2) has a profound impact on HIV-1 replication in the Hu-PBL-SCID mouse model. 9th Conf. Retrovir. Opportunistic Infect. A410-T (2002).
-
(2002)
9th Conf. Retrovir. Opportunistic Infect.
-
-
Franti, M.1
-
70
-
-
0033914939
-
Single-dose safety, pharmacology, and antiviral activity of the human immunodeficiency virus (HIV) type 1 entry inhibitor PRO 542 in HIV-infected adults
-
Jacobson, J. M. et al. Single-dose safety, pharmacology, and antiviral activity of the human immunodeficiency virus (HIV) type 1 entry inhibitor PRO 542 in HIV-infected adults. J. Infect. Dis. 182, 326-329 (2000).
-
(2000)
J. Infect. Dis.
, vol.182
, pp. 326-329
-
-
Jacobson, J.M.1
-
71
-
-
25744431848
-
Mechanisms of synergy between HIV-1 attachment, coreceptor and fusion inhibitors
-
Nagashima, K. et al. Mechanisms of synergy between HIV-1 attachment, coreceptor and fusion inhibitors. 8th Conf. Retrovir. Opportunistic Infect. A310 (2001).
-
(2001)
8th Conf. Retrovir. Opportunistic Infect.
-
-
Nagashima, K.1
-
72
-
-
0006714139
-
Potent, synergistic inhibition of HIV-1 by combinations of the viral entry inhibitors PRO-542 and T-20
-
Olson, W. C. et al. Potent, synergistic inhibition of HIV-1 by combinations of the viral entry inhibitors PRO-542 and T-20. 40th Intersci. Conf. Antimicrob. Agents Chemother. A549 (2000).
-
(2000)
40th Intersci. Conf. Antimicrob. Agents Chemother.
-
-
Olson, W.C.1
-
73
-
-
0028865465
-
Cross-clade neutralization of primary isolates of human immunodeficiency virus type 1 by human monoclonal antibodies and tetrameric CD4-IgG
-
Trkola, A. et al. Cross-clade neutralization of primary isolates of human immunodeficiency virus type 1 by human monoclonal antibodies and tetrameric CD4-IgG. J. Virol. 69, 6609-6617 (1995).
-
(1995)
J. Virol.
, vol.69
, pp. 6609-6617
-
-
Trkola, A.1
-
74
-
-
0034625144
-
A binding pocket for a small molecule inhibitor of HIV-1 entry within the transmembrane helices of CCR5
-
Dragic, T. et al. A binding pocket for a small molecule inhibitor of HIV-1 entry within the transmembrane helices of CCR5. Proc. Natl Acad. Sci. USA 97, 5639-5644 (2000).
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 5639-5644
-
-
Dragic, T.1
-
75
-
-
0035180230
-
Inhibitory effects of small-molecule CCR5 antagonists on human immunodeficiency virus type 1 envelope-mediated membrane fusion and viral replication
-
Takashima, K. et al. Inhibitory effects of small-molecule CCR5 antagonists on human immunodeficiency virus type 1 envelope-mediated membrane fusion and viral replication. Antimicrob. Agents Chemother. 45, 3538-3543 (2001).
-
(2001)
Antimicrob. Agents Chemother.
, vol.45
, pp. 3538-3543
-
-
Takashima, K.1
-
76
-
-
0003229490
-
In vitro synergy observed between the fusion inhibitor T-20 and a CCR5 inhibitor TAK-779
-
Tremblay, C. L. et al. In vitro synergy observed between the fusion inhibitor T-20 and a CCR5 inhibitor TAK-779. 40th Intersci. Conf. Antimicrob. Agents Chemother. A1164 (2000).
-
(2000)
40th Intersci. Conf. Antimicrob. Agents Chemother.
-
-
Tremblay, C.L.1
-
77
-
-
1642300963
-
TAK-220, a novel small molecular inhibitor of CCR5 has favorable anti-HIV interactions with other antiretrovirals in vitro
-
Tremblay, C. L. et al. TAK-220, a novel small molecular inhibitor of CCR5 has favorable anti-HIV interactions with other antiretrovirals in vitro. 10th Conf. Retrovir. Opportunistic Infect. A562 (2003).
-
(2003)
10th Conf. Retrovir. Opportunistic Infect.
-
-
Tremblay, C.L.1
-
78
-
-
0011937519
-
The CCR5 co-receptor inhibitor PRO 140 effectively controls established HIV-1 infections in vivo
-
A403-T
-
Franti, M. et al. The CCR5 co-receptor inhibitor PRO 140 effectively controls established HIV-1 infections in vivo. 9th Conf. Retrovir. Opportunistic Infect. A403-T (2002).
-
(2002)
9th Conf. Retrovir. Opportunistic Infect.
-
-
Franti, M.1
-
79
-
-
0036232981
-
Anti-human immunodeficiency virus interactions of SCH-C (SCH 351125), a CCR5 antagonist, with other antiretroviral agents in vitro
-
Tremblay, C. L. et al. Anti-human immunodeficiency virus interactions of SCH-C (SCH 351125), a CCR5 antagonist, with other antiretroviral agents in vitro. Antimicrob. Agents Chemother. 46, 1336-1339 (2002).
-
(2002)
Antimicrob. Agents Chemother.
, vol.46
, pp. 1336-1339
-
-
Tremblay, C.L.1
-
80
-
-
0345700287
-
Entry inhibitors SCH-C, RANTES, and T-20 block HIV type 1 replication in multiple cell types
-
Ketas, T. J. et al. Entry inhibitors SCH-C, RANTES, and T-20 block HIV type 1 replication in multiple cell types. AIDS Res. Hum. Retroviruses 19, 177-186 (2003).
-
(2003)
AIDS Res. Hum. Retroviruses
, vol.19
, pp. 177-186
-
-
Ketas, T.J.1
-
81
-
-
1642362762
-
Genotypic and phenotypic analysis of in vitro generated HIV-1 escape isolates to the CCR5 antagonist SCH-C
-
A397-T
-
Riley, J. et al. Genotypic and phenotypic analysis of in vitro generated HIV-1 escape isolates to the CCR5 antagonist SCH-C. 9th Conf. Retrovir. Opportunistic Infect. A397-T (2002).
-
(2002)
9th Conf. Retrovir. Opportunistic Infect.
-
-
Riley, J.1
-
83
-
-
0007551002
-
Strong in vitro synergy observed between the fusion inhibitor T-20 and a CXCR4 blocker AMD-3100
-
Tremblay, C. et al. Strong in vitro synergy observed between the fusion inhibitor T-20 and a CXCR4 blocker AMD-3100. 7th Conf. Retrovir. Opportunistic Infect. A500 (2000)
-
(2000)
7th Conf. Retrovir. Opportunistic Infect.
-
-
Tremblay, C.1
-
84
-
-
0037539520
-
Enfuvirtide (T-20) and T-1249 resistance: Observations from Phase II clinical trials of enfuvirtide in combination with oral antiretrovirals (ARVs) and a Phase I/II dose-ranging monotherapy trial of T-1249
-
Greenberg, M. L. et al. Enfuvirtide (T-20) and T-1249 resistance: Observations from Phase II clinical trials of enfuvirtide in combination with oral antiretrovirals (ARVs) and a Phase I/II dose-ranging monotherapy trial of T-1249. 11th Int. HIV Drug Resist. Workshop. A128 (2002).
-
(2002)
11th Int. HIV Drug Resist. Workshop.
-
-
Greenberg, M.L.1
-
85
-
-
0003279235
-
Complete analysis of T1249-101: Safety, pharmacokinetics, and antiviral activity of T-1249, a peptide inhibitor of HIV membrane fusion
-
Gulick, R. et al. Complete analysis of T1249-101: Safety, pharmacokinetics, and antiviral activity of T-1249, a peptide inhibitor of HIV membrane fusion. 42nd Intersci. Conf. Antimicrob. Agents Chemother. A850 (2002).
-
(2002)
42nd Intersci. Conf. Antimicrob. Agents Chemother.
-
-
Gulick, R.1
-
86
-
-
25744469619
-
Baseline genotype and prior antiretroviral history do not affect virological response to T-1249
-
Miralles, G. D. et al. Baseline genotype and prior antiretroviral history do not affect virological response to T-1249. 5th Int. Workshop HIV Drug Resist. Treat. Strateg. A3 (2001).
-
(2001)
5th Int. Workshop HIV Drug Resist. Treat. Strateg.
-
-
Miralles, G.D.1
-
87
-
-
0013369081
-
Genotypic resistance to protease and reverse transcriptase inhibitors and antiretroviral history do not affect virologic response to T-1249
-
Miralles, G. D. et al. Genotypic resistance to protease and reverse transcriptase inhibitors and antiretroviral history do not affect virologic response to T-1249. 41st Intersci. Conf. Antimicrob. Agents Chemother. A669 (2001).
-
(2001)
41st Intersci. Conf. Antimicrob. Agents Chemother.
-
-
Miralles, G.D.1
-
88
-
-
0036050539
-
Strategies in the design of antiviral drugs
-
De Clercq, E. Strategies in the design of antiviral drugs. Nature Rev. Drug Disc. 1, 13-25 (2002).
-
(2002)
Nature Rev. Drug Disc.
, vol.1
, pp. 13-25
-
-
De Clercq, E.1
|