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Odalasvir is an investigational, orally administered, second-generation small molecule inhibitor of the hepatitis C virus (HCV) nonstructural protein 5A (NS5A). NS5A is a multifunctional viral protein essential for HCV replication and plays a role in interferon resistance. By inhibiting NS5A, odalasvir disrupts viral replication and can help overcome treatment failure associated with interferon-based therapies. Odalasvir was developed by Achillion Pharmaceuticals and has been studied primarily for the treatment of chronic hepatitis C infection, including in combination regimens with other direct acting antivirals such as adafosbuvir (AL-335) and simeprevir. Clinical development reached phase II trials but was subsequently discontinued[1][3][7].
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