Daclatasvir: The First
of a New Class of Drugs Targeted Against Hepatitis C Virus NS5A
Author(s):
I. Gentile, F. Borgia, N. Coppola, A.R.
Buonomo, G. Castaldo and G. Borgia Pages 1391-1404 (14)
Abstract:
Hepatitis C virus (HCV) infection affects
about 160 million people worldwide. It is treated with pegylatedinterferon
(peg-IFN) and ribavirin, and in the case of patients affected by genotype 1,
also with a protease inhibitor (telaprevir or boceprevir). Despite a good
success rate, IFN-based combinations are contraindicated in several patients
(e.g. decompensated cirrhosis, patients with psychiatric disorders, severe
heart diseases or autoimmune disorders) and are associated with frequent
adverse events that ultimately reduce their use. Numerous oral drugs are in an
advanced phase of clinical development, and in some cases, in IFN-free
combinations. This review focuses on preclinical and clinical data regarding
daclatasvir (BMS-790052), which is a highly selective HCV NS5A replication
complex inhibitor effective against HCV genotypes 1, 2, 3 and 4. In vitro data
show that daclatasvir exerts a very potent antiviral effect against several HCV
genotypes. Its pharmacokinetics is optimal and allows once-a-day oral administration.
Its adverse event profile is good. Clinical data regarding its efficacy in
combination with peg-IFN, ribavirin or other direct antiviral agents are
impressive (rates of sustained virological response range between 60% and 100%
in treatment-naïve patients). The only drawback of this drug appears to be a
relatively low genetic barrier to resistance. In conclusion, daclatasvir,
especially in combinations with other antiviral agents, is a very promising
drug for the treatment of chronic hepatitis C.
Keywords:
Combination therapy, daclatasvir, hepatitis C
virus, Interferon-free, pegylated-interferon, polymerase inhibitors,
resistance, ribavirin.
Affiliation:
Department of Clinical Medicine and Surgery
(Ed. 18) – University of Naples “Federico II”, via S. Pansini, 5 I-80131
Naples, Italy.
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