Catalyst Pharmaceuticals Inc. on Thursday said the U.S. Food and Drug Administration approved the expanded use of its Firdapse treatment for Lambert-Eaton myasthenic syndrome to include children.
The Coral Gables, Fla., biopharmaceutical company said the drug is now available for patients ages 6 through 17 with the rare condition, in which the immune system attacks the neuromuscular junctions.
In 2018, the FDA approved Firdapse for adults with Lambert-Eaton myasthenic syndrome.
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