Drug class
Hepatitis C Nucleos(t)ide Analog NS5B Polymerase Inhibitors
Hepatitis C nucleos(t)ide analog NS5B polymerase inhibitors are a therapeutic class of direct-acting antiviral agents utilized primarily for the management and cure of chronic hepatitis C virus infection. Read more about Hepatitis C Nucleos(t)ide Analog NS5B Polymerase Inhibitors
6 drugs in this class 2 manufacturers
Drugs in Hepatitis C Nucleos(t)ide Analog NS5B Polymerase Inhibitors
HARVONI (ledipasvir/sofosbuvir)
EPCLUSA (sofosbuvir/velpatasvir)
VOSEVI (sofosbuvir/velpatasvir/voxilaprevir)
LEDIPASVIR-SOFOSBUVIR (ledipasvir/sofosbuvir)
SOFOSBUVIR-VELPATASVIR (sofosbuvir/velpatasvir)
Hepatitis C nucleos(t)ide analog NS5B polymerase inhibitors are a therapeutic class of direct-acting antiviral agents utilized primarily for the management and cure of chronic hepatitis C virus infection.
Administered as prodrugs, these agents are intracellularly converted into pharmacologically active triphosphate forms that mimic natural nucleotides and bind directly to the conserved catalytic active site of the viral RNA-dependent RNA polymerase.
By competing with physiological substrates, they induce premature viral RNA chain termination, thereby halting viral replication.
Because their target site is highly conserved across viral genotypes, members of this class typically display pangenotypic antiviral activity and a high genetic barrier to resistance.
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nih.gov
Hepatitis C nucleos(t)ide analog NS5B polymerase inhibitors are a therapeutic class of direct-acting antiviral agents utilized primarily for the management and cure of chronic hepatitis C virus infection
-
nih.gov
Hepatitis C nucleos(t)ide analog NS5B polymerase inhibitors are a therapeutic class of direct-acting antiviral agents utilized primarily for the management and cure of chronic hepatitis C virus infection Administered as prodrugs, these agents are intracellularly converted into pharmacologically active triphosphate forms that mimic natural nucleotides and bind directly to the conserved catalytic active site of the viral RNA-dependent RNA polymerase By competing with physiological substrates, they...
-
nih.gov
Administered as prodrugs, these agents are intracellularly converted into pharmacologically active triphosphate forms that mimic natural nucleotides and bind directly to the conserved catalytic active site of the viral RNA-dependent RNA polymerase Because their target site is highly conserved across viral genotypes, members of this class typically display pangenotypic antiviral activity and a high genetic barrier to resistance
-
nih.gov
Administered as prodrugs, these agents are intracellularly converted into pharmacologically active triphosphate forms that mimic natural nucleotides and bind directly to the conserved catalytic active site of the viral RNA-dependent RNA polymerase By competing with physiological substrates, they induce premature viral RNA chain termination, thereby halting viral replication
-
nih.gov
Because their target site is highly conserved across viral genotypes, members of this class typically display pangenotypic antiviral activity and a high genetic barrier to resistance
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