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BioWorld - Saturday, July 6, 2024
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» Genentech’s Piasky cleared for paroxysmal nocturnal hemoglobinuria
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Genentech’s Piasky cleared for paroxysmal nocturnal hemoglobinuria
June 24, 2024
By
Karen Carey
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Roche Holding AG’s Genentech Inc. unit received U.S. FDA approval on June 20 of Piasky (crovalimab) to treat adults and children 13 and older with paroxysmal nocturnal hemoglobinuria and a body weight of at least 40 kg (88 pounds).
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