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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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8 Plus, these drugs improve blood sugar control, which helps to reduce fatigue caused by post-meal spikes and crashes, especially in those with insulin resistance or diabetes

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