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AstraZeneca's Voydeya granted EC approval to treat rare blood disease PNH

AstraZeneca's Voydeya granted EC approval to treat rare blood disease PNH
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Facit
Lancashire
United-kingdom
Marc-dunoyer
European-commission
European-medicines-agency
Drug-administration

AstraZeneca (AZN) Announces Voydeya Approval in EU as add-on to ravulizumab or eculizumab

AstraZeneca (AZN) Announces Voydeya Approval in EU as add-on to ravulizumab or eculizumab
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Committee-for-medicinal-products-human
University-of-ulm
Drug-administration
European-medicines-agency
European-union
European-commission
Institute-of-transfusion-medicine
Medicinal-products

FDA Approves Danicopan With C5 Inhibitor Therapy to Treat EVH in Adults With Paroxysmal Nocturnal Hemoglobinuria

Positive phase 3 trial results showed that danicopan was more effective than placebo when treating extravascular hemolysis in paroxysmal nocturnal hemoglobinuria.

United-states
Japan
Bart-scott
Marc-dunoyer
Division-of-hematology
University-of-washington-medical-center
Alexion-pharmaceuticals-inc
Astrazeneca
Add-on-therapy
Paroxysmal-nocturnal-hemoglobinuria
Alexion-pharmaceuticals
Washington-medical-center

AstraZeneca: FDA approves Voydeya to treat HPN -April 02, 2024 at 04:49 am EDT

AstraZeneca announces that Voydeya has been approved in the U.S. as an adjunctive therapy to Ultomiris or Soliris in the treatment of extravascular hemolysis in adults with paroxysmal nocturnal.

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