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EFPIA companies in kind contribution. IMPORTANT SAFETY INFORMATION FOR ABRYSVOABRYSVO is a Phase 3, prospective, randomized, multicenter, open-label, parallel group comparative study conducted with 422 hospitalized adult patients across 81 locations in 9 countries. No patient treated with ATM-AVI experienced a treatment-related SAE. Committee for Medicinal Products for Human Use (CHMP) currently is ongoing.

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