Ultomiris approved in Europe to treat rare neuromuscular disorder
Developed by UK pharma major AstraZeneca (LSE: AZN), Ultomiris (ravulizumab) has been approved in Europe for a new indication.
The monoclonal antibody has been approved as an add-on to standard therapy for the treatment of adults with generalized myasthenia gravis (gMG) who are anti-acetylcholine receptor antibody-positive.
Last year, Ultomiris was approved in the European Union for expanded use to include children—with a body weight of 10kg or above—and adolescents with paroxysmal nocturnal hemoglobinuria, and prior to that also for adults.
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