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Albinterferon alfa-2a is a **long-acting recombinant fusion protein drug** consisting of interferon alpha-2a covalently linked to human serum albumin. This design greatly extends its half-life, enabling dosing once every two to four weeks, compared to more frequent administration with conventional interferons or peginterferon. The mechanism of action is typical of type I interferons: albinterferon alfa-2a binds to the interferon alpha/beta receptor (IFNAR1/2) on cells, activating the JAK/STAT pathway, thereby inducing an array of antiviral, antiproliferative, and immunomodulatory genes. It was developed for chronic hepatitis C as an alternative to peginterferon alfa-2a, but global development was discontinued due to safety concerns and business decisions following adverse events in clinical trials[8][2].
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