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TQ-A3326 is a small molecule antiviral drug developed as a deuterated analog of daclatasvir, specifically designed to inhibit the hepatitis C virus (HCV) NS5A protein. By modifying daclatasvir with deuterium, TQ-A3326 aims to improve pharmacokinetic properties and metabolic stability. The drug has been evaluated in healthy volunteers for its pharmacokinetics, metabolism, and tolerability. Fecal excretion is the predominant route of elimination for TQ-A3326 and its metabolites. Its primary indication is for the treatment of hepatitis C virus infection.
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