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Sanofis results from the Phase 2 study showed that efdoralprin alfa, a recombinant human alpha-1 antitrypsin (AAT)-Fc fusion protein therapy met all primary and key secondary endpoints when dosed every 3 weeks or 4 weeks in adults with alpha-1 antitrypsin deficiency (AATD) emphysema (a rare disease), offering a more convenient and potentially more effective option

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2016, Article ID 4389410, 14 pages, 2016

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