European approval for Voydeya adds to AstraZeneca's lead in PNH
A first-in-class treatment for paroxysmal nocturnal hemoglobinuria (PNH), Voydeya (danicopan), has been granted marketing authorization in Europe.
The therapy is approved as an add-on to AstraZeneca’s (LSE: AZN) other options, Ultomiris (ravulizumab) or Soliris (eculizumab), for the treatment of adults with PNH, a rare, chronic, progressive and potentially life-threatening blood disorder.
The treatment represents an important new option for a subset of patients with PNH who experience anemia despite treatment with a C5 blocker.
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