Catalyst Pharma files lawsuit against USFDA challenging approval of Ruzurgi
Ruzurgi was approved last month for treating Lambert-Eaton myasthenic syndrome that affects about one in 100,000 people in the United States.
U.S: Catalyst Pharmaceuticals Inc said on Wednesday it has filed a lawsuit against the U.S. Food and Drug Administration, challenging the recent approval of Jacobus Pharmaceutical Co's drug, Ruzurgi, for a rare neuromuscular disease.
Ruzurgi was approved last month for treating Lambert-Eaton myasthenic syndrome that affects about one in 100,000 people in the United States.
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Catalyst PharmaCatalyst PharmaceuticalsJacobus PharmaLambert Eaton Myasthenic Syndromelawsuitrare neuromuscular diseaseRuzurgiUnited StatesUSFDA
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