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Sofosbuvir + ledipasvir and sofosbuvir + daclatasvir are two potent oral, small-molecule, direct-acting antiviral (DAA) combination regimens used for the treatment of chronic hepatitis C virus (HCV) infection. Sofosbuvir is a pangenotypic nucleotide analog inhibitor of the HCV NS5B RNA-dependent RNA polymerase, which is essential for viral replication. Ledipasvir and daclatasvir are both inhibitors of the HCV NS5A protein, a multifunctional protein involved in viral RNA replication and the assembly of HCV virions. The sofosbuvir/ledipasvir combination is marketed as a fixed-dose single tablet (Harvoni, developed by Gilead Sciences), while sofosbuvir/daclatasvir involves the co-administration of two separate drugs (Sovaldi and Daklinza, developed by Gilead and Bristol Myers Squibb, respectively). These regimens have revolutionized HCV treatment, offering high cure rates (SVR12 >90%) with a favorable safety profile and a typical treatment duration of 12 weeks. In Egypt, these DAAs have been central to the national campaign to eliminate HCV, particularly targeting genotype 4, which is predominant in the region.
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