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Europe Approves Paroxysmal Nocturnal Hemoglobinuria Drug

The factor D inhibitor danicopan has been approved for use in Europe for patients with paroxysmal nocturnal hemoglobinuria with residual hemolytic anemia on standard therapy.

European unionEuropean medicines agencyEuropean commissionDrug administrationPriority medicinesMedicinal productsHuman useParoxysmal nocturnal hemoglobinuriaNh paroxysmal nocturnal hemoglobinuriaParoxysmal nocturnal haemoglobinuriaParoxysmal nocturnal hemoglobinuria pnhHemolytic anemia haemolytic anaemiaAnemia anaemiaBiologic therapyGenomics genomic medicineOrphan drugs

FDA OKs Danicopan for Extravascular Hemolysis in PNH

A tablet has been approved for a common complication during treatment for a rare blood disorder.

Drug administrationRisk evaluationMitigation strategyPatient safetyBlood transfusionBlood clotBiliary diseaseAllbladder diseaseParoxysmal nocturnal hemoglobinuriaNh paroxysmal nocturnal hemoglobinuriaParoxysmal nocturnal haemoglobinuriaParoxysmal nocturnal hemoglobinuria pnhCovid 19019 novel coronavirus019 ncovUhan coronavirus

FDA OKs Iptacopan to Treat Paroxysmal Nocturnal Hemoglobinuria

This marks the first oral monotherapy approved for the rare blood disorder.

United statesVinod pullarkatDrug administrationCity of hope cancer centerHope cancer centerRisk evaluationMitigation strategyParoxysmal nocturnal hemoglobinuriaNh paroxysmal nocturnal hemoglobinuriaParoxysmal nocturnal haemoglobinuriaPrimary immunodeficiencyPrimary immunodeficienciesNt specialtyEad and neck surgery ent specialityCovid 19019 novel coronavirus

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