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Novartis announced FDA approval for Fabhalta

Novartis announced FDA approval for Fabhalta
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Vinod pullarkatDrug administrationDepartment of hematologyClinical professorHematopoietic cell transplantation

Novartis Fabhalta approved by FDA as first oral monotherapy for rare blood disease PNH

Novartis Fabhalta approved by FDA as first oral monotherapy for rare blood disease PNH
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Novarti cosentyxVinod pullarkatNovarti fabhaltaDrug administration

FDA Approves Iptacopan for the Treatment of Paroxysmal Nocturnal Hemoglobinuria in Adult Patients

During clinical trials, individuals treated with iptacopan had increased hemoglobin levels and did not need to receive blood transfusions.

Vinod pullarkatVictor bult

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

FDA Approves Oral Factor B Inhibitor for Paroxysmal Nocturnal Hemoglobinuria

Iptacopan tops C5 Inhibitors for sustained hemoglobin levels, eliminating need for transfusion

United statesVinod pullarkat

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