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Maraviroc for Previously Treated Patients with R5 HIV-1 Infection
by
Nadler, Jeffrey
, Lalezari, Jacob
, Felstead, Steve
, Karlsson, Anders
, Montana, John B
, Sullivan, John
, Mayer, Howard
, Clotet, Bonaventura
, van der Ryst, Elna
, DeJesus, Edwin
, Wohlfeiler, Michael
, McHale, Mary
, Clumeck, Nathan
, Horban, Andrzej
, Ridgway, Caroline
, Goodrich, James
, Gulick, Roy M
, Dunne, Michael W
in
Adult
/ Aged
/ Anti-Retroviral Agents - adverse effects
/ Anti-Retroviral Agents - therapeutic use
/ Anti-Retroviral Agents/adverse effects/therapeutic use
/ Antiretroviral drugs
/ Biological and medical sciences
/ CCR5 Receptor Antagonists
/ CD4 Lymphocyte Count
/ Cyclohexanes - adverse effects
/ Cyclohexanes - therapeutic use
/ Cyclohexanes/adverse effects/therapeutic use
/ Double-Blind Method
/ Drug resistance
/ Drug Resistance, Viral
/ Drug therapy
/ Drug Therapy, Combination
/ Female
/ General aspects
/ HIV
/ HIV Fusion Inhibitors - adverse effects
/ HIV Fusion Inhibitors - therapeutic use
/ HIV Fusion Inhibitors/adverse effects/therapeutic use
/ HIV Infections - drug therapy
/ HIV Infections - virology
/ HIV Infections/drug therapy/virology
/ HIV-1 - chemistry
/ HIV-1 - genetics
/ HIV-1/chemistry/genetics
/ Human health sciences
/ Human immunodeficiency virus
/ Human viral diseases
/ Humans
/ Immunologie & maladie infectieuse
/ Immunology & infectious disease
/ Infectious diseases
/ Male
/ Maraviroc
/ Medical sciences
/ Middle Aged
/ Receptors, CCR5/antagonists & inhibitors
/ RNA, Viral - blood
/ Sciences de la santé humaine
/ Treatment Failure
/ Triazoles - adverse effects
/ Triazoles - therapeutic use
/ Triazoles/adverse effects/therapeutic use
/ Viral diseases
/ Viral diseases of the lymphoid tissue and the blood. Aids
/ Viral Load
2008
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Maraviroc for Previously Treated Patients with R5 HIV-1 Infection
by
Nadler, Jeffrey
, Lalezari, Jacob
, Felstead, Steve
, Karlsson, Anders
, Montana, John B
, Sullivan, John
, Mayer, Howard
, Clotet, Bonaventura
, van der Ryst, Elna
, DeJesus, Edwin
, Wohlfeiler, Michael
, McHale, Mary
, Clumeck, Nathan
, Horban, Andrzej
, Ridgway, Caroline
, Goodrich, James
, Gulick, Roy M
, Dunne, Michael W
in
Adult
/ Aged
/ Anti-Retroviral Agents - adverse effects
/ Anti-Retroviral Agents - therapeutic use
/ Anti-Retroviral Agents/adverse effects/therapeutic use
/ Antiretroviral drugs
/ Biological and medical sciences
/ CCR5 Receptor Antagonists
/ CD4 Lymphocyte Count
/ Cyclohexanes - adverse effects
/ Cyclohexanes - therapeutic use
/ Cyclohexanes/adverse effects/therapeutic use
/ Double-Blind Method
/ Drug resistance
/ Drug Resistance, Viral
/ Drug therapy
/ Drug Therapy, Combination
/ Female
/ General aspects
/ HIV
/ HIV Fusion Inhibitors - adverse effects
/ HIV Fusion Inhibitors - therapeutic use
/ HIV Fusion Inhibitors/adverse effects/therapeutic use
/ HIV Infections - drug therapy
/ HIV Infections - virology
/ HIV Infections/drug therapy/virology
/ HIV-1 - chemistry
/ HIV-1 - genetics
/ HIV-1/chemistry/genetics
/ Human health sciences
/ Human immunodeficiency virus
/ Human viral diseases
/ Humans
/ Immunologie & maladie infectieuse
/ Immunology & infectious disease
/ Infectious diseases
/ Male
/ Maraviroc
/ Medical sciences
/ Middle Aged
/ Receptors, CCR5/antagonists & inhibitors
/ RNA, Viral - blood
/ Sciences de la santé humaine
/ Treatment Failure
/ Triazoles - adverse effects
/ Triazoles - therapeutic use
/ Triazoles/adverse effects/therapeutic use
/ Viral diseases
/ Viral diseases of the lymphoid tissue and the blood. Aids
/ Viral Load
2008
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Maraviroc for Previously Treated Patients with R5 HIV-1 Infection
by
Nadler, Jeffrey
, Lalezari, Jacob
, Felstead, Steve
, Karlsson, Anders
, Montana, John B
, Sullivan, John
, Mayer, Howard
, Clotet, Bonaventura
, van der Ryst, Elna
, DeJesus, Edwin
, Wohlfeiler, Michael
, McHale, Mary
, Clumeck, Nathan
, Horban, Andrzej
, Ridgway, Caroline
, Goodrich, James
, Gulick, Roy M
, Dunne, Michael W
in
Adult
/ Aged
/ Anti-Retroviral Agents - adverse effects
/ Anti-Retroviral Agents - therapeutic use
/ Anti-Retroviral Agents/adverse effects/therapeutic use
/ Antiretroviral drugs
/ Biological and medical sciences
/ CCR5 Receptor Antagonists
/ CD4 Lymphocyte Count
/ Cyclohexanes - adverse effects
/ Cyclohexanes - therapeutic use
/ Cyclohexanes/adverse effects/therapeutic use
/ Double-Blind Method
/ Drug resistance
/ Drug Resistance, Viral
/ Drug therapy
/ Drug Therapy, Combination
/ Female
/ General aspects
/ HIV
/ HIV Fusion Inhibitors - adverse effects
/ HIV Fusion Inhibitors - therapeutic use
/ HIV Fusion Inhibitors/adverse effects/therapeutic use
/ HIV Infections - drug therapy
/ HIV Infections - virology
/ HIV Infections/drug therapy/virology
/ HIV-1 - chemistry
/ HIV-1 - genetics
/ HIV-1/chemistry/genetics
/ Human health sciences
/ Human immunodeficiency virus
/ Human viral diseases
/ Humans
/ Immunologie & maladie infectieuse
/ Immunology & infectious disease
/ Infectious diseases
/ Male
/ Maraviroc
/ Medical sciences
/ Middle Aged
/ Receptors, CCR5/antagonists & inhibitors
/ RNA, Viral - blood
/ Sciences de la santé humaine
/ Treatment Failure
/ Triazoles - adverse effects
/ Triazoles - therapeutic use
/ Triazoles/adverse effects/therapeutic use
/ Viral diseases
/ Viral diseases of the lymphoid tissue and the blood. Aids
/ Viral Load
2008
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Maraviroc for Previously Treated Patients with R5 HIV-1 Infection
Journal Article
Maraviroc for Previously Treated Patients with R5 HIV-1 Infection
2008
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Overview
The CCR5 coreceptor may be a therapeutic target to block HIV infection. HIV-1–infected patients who had received previous antiretroviral treatment were enrolled in one of two phase 3, placebo-controlled, double-blind international studies of treatment with maraviroc (a CCR5 antagonist). Maraviroc significantly lowered the HIV-1 viral load and increased the CD4 cell count at 48 weeks.
The CCR5 coreceptor may be a therapeutic target to block HIV infection. In two studies, maraviroc (a CCR5 antagonist) significantly lowered the HIV-1 viral load and increased the CD4 cell count at 48 weeks.
For the past decade, treatment of human immunodeficiency virus type 1 (HIV-1) has consisted of a multiple-drug regimen targeting one or more of three HIV-1 proteins: reverse transcriptase, protease, and the glycoprotein envelope subunit gp41.
1
Although these antiretroviral combinations are successful in suppressing viral replication and delaying disease progression, drug resistance and toxic effects may occur.
2
–
4
There is therefore a need for better-tolerated, convenient antiretroviral agents with reduced toxicity and activity against multidrug-resistant viruses.
Agents with novel mechanisms of action provide options for patients with drug-resistant virus.
4
CC chemokine receptor 5 (CCR5) is an attractive therapeutic target, since people . . .
Publisher
Massachusetts Medical Society
Subject
/ Aged
/ Anti-Retroviral Agents - adverse effects
/ Anti-Retroviral Agents - therapeutic use
/ Anti-Retroviral Agents/adverse effects/therapeutic use
/ Biological and medical sciences
/ Cyclohexanes - adverse effects
/ Cyclohexanes - therapeutic use
/ Cyclohexanes/adverse effects/therapeutic use
/ Female
/ HIV
/ HIV Fusion Inhibitors - adverse effects
/ HIV Fusion Inhibitors - therapeutic use
/ HIV Fusion Inhibitors/adverse effects/therapeutic use
/ HIV Infections - drug therapy
/ HIV Infections/drug therapy/virology
/ Human immunodeficiency virus
/ Humans
/ Immunologie & maladie infectieuse
/ Immunology & infectious disease
/ Male
/ Receptors, CCR5/antagonists & inhibitors
/ Sciences de la santé humaine
/ Triazoles/adverse effects/therapeutic use
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