(Reuters) - Apellis Pharmaceuticals Inc said on Tuesday its experimental drug for a blood disorder showed greater improvement in patients' hemoglobin levels than market leader Alexion Pharmaceuticals ...
With a patent challenge for blockbuster Soliris underway, Alexion is working hard to expand the reach of its successor drug Ultomiris. With one carry-over indication already in the bag, Ultomiris just ...
Alexion Pharmaceuticals said it has won an orphan-drug designation from the U.S. Food and Drug Administration for its commercial drug Soliris. Orphan drug designations are meant to incentivize ...
Please provide your email address to receive an email when new articles are posted on . The U.S. Food and Drug Administration has granted an orphan drug designation to Alexion Pharmaceuticals' Soliris ...
FDA Grants Orphan Drug Designation to Soliris(R) (eculizumab) for Prevention of Delayed Graft Function (DGF) in Renal Transplant Patients Alexion Pharmaceuticals (Nasdaq:ALXN) today announced that the ...
EMA committee separately recommended approval of drug for same indication in Europe. FDA approved Alexion Pharmaceuticals’ Soliris™ (eculizumab) for the treatment of pediatric and adult patients with ...
Leerink Swann analyst Howard Liang reaffirmed an "outperform" rating for Cheshire-based Alexion Pharmaceuticals Inc. today, citing the future revenue potential for its key drug Soliris. Soliris, ...
Alexion announced that the FDA has granted Orphan Drug designation to Soliris (eculizumab), a first-in-class terminal complement inhibitor for the prevention of delayed graft function (DGF) in renal ...
CHESHIRE, Conn.--(BUSINESS WIRE)-- Alexion Pharmaceuticals, Inc. (NAS: ALXN) today announced that Soliris ® (eculizumab), the company's first-in-class terminal complement inhibitor, has been granted ...
(CBS) The FDA has approved the drug Soliris (eculizumab) for the treatment of a rare and potentially deadly blood disease known as atypical hemolytic uremic syndrome (aHUS). There are no other ...
Alexion announced that Soliris (eculizumab), a first-in-class terminal complement inhibitor, has been granted an Orphan Drug designation by the FDA for the treatment of neuromyelitis optica (NMO), a ...