Voydeya (danicopan) has been approved in the European Union (EU) as an add-on to ravulizumab or eculizumab for the treatment of adult patients with paroxysmal nocturnal haemoglobinuria (PNH) who have residual haemolytic anaemia.1 Voydeya is a first-in-class, oral, Factor D inhibitor developed as an add-on to standard-of-care Ultomiris (ravulizumab) or Soliris (eculizumab) to address the needs of the approximately 10-20% of patients with PNH who experience clinically significant extravascular haemolysis (EVH) while treated with a C5 inhibitor.2,3
Lights, camera, Alexion! Fresh off an FDA approval for Ultomiris in NMOSD, AstraZeneca’s rare disease unit has put out a film sharing patient stories.
LOUISVILLE, Ky., April 08, 2024 (GLOBE NEWSWIRE) -- Onco360®, the nation's leading independent Specialty Pharmacy, has been selected as a national pharmacy partner by Alexion Pharmaceuticals for...
FDA clears AZ’s new PNH therapy Voydeya
FDA expands AZ`s Ultomiris to NMOSD after prior rejection
ULTOMIRIS approved in the US for the treatment of adults with NMOSD
Voydeya recommended for approval in the EU by CHMP
Alexion Pharma`s Biologic Ultomiris (ravulizumab) Receives Approval in the U.S.
PIII trial data showed danicopan as add-on to ULTOMIRIS sustained improvements
The FDA has denied AstraZeneca’s supplemental application for its C5 complement inhibitor Ultomiris (ravulizumab-cwvz), seeking approval for the treatment of adults with neuromyelitis optica spectrum disorder, the company announced Wednesday.