Prilenia Plans to Submit Marketing Authorization Application (MAA) in the EU for Pridopidine in Huntington’s Disease
“Pridopidine demonstrates consistent treatment benefits across independent measures that are important to patients and families.
- “Pridopidine demonstrates consistent treatment benefits across independent measures that are important to patients and families.
- The benefits are clearly evident in those with HD who are not taking anti-dopaminergic medications (ADM),” said Dr. Michael R. Hayden, CEO of Prilenia.
- “We appreciate the constructive discussions with European regulators regarding our data for pridopidine.
- The Company will also consider global regulatory submissions for additional countries and regions following the regulatory review process in Europe.