Prilenia to Present Latest Research from its Pridopidine Programs for Huntington Disease and ALS at AAN 2024
Prilenia Plans to Submit MAA in the EU for Pridopidine in Huntington’s Disease
Aural Analytics Speech Technology Signaled Slowing of Decline in ALS Patients’ Speech and Bulbar Function in Platform Trial Evaluating Pridopidine
Prilenia Therapeutics’ amyotrophic lateral sclerosis (ALS) therapy did not improve disease severity, but the biotech is pointing to “positive trends” from an exploratory analysis, suggesting that some patients' experienced a slower decline.
NAARDEN, The Netherlands--(BUSINESS WIRE)--Prilenia Therapeutics B.V., a clinical stage biotech company focused on developing novel treatments for neurodegenerative and neurodevelopmental disorders, today announced the completion of participant enrollment in the pridopidine arm of the HEALEY ALS Platform Trial. The trial is led by the Sean M. Healey & AMG Center for ALS at Massachusetts General Hospital and is designed to evaluate the safety and efficacy of multiple drug candidates in people with Amyotrophic Lateral Sclerosis (ALS).
NAARDEN, Netherlands--(BUSINESS WIRE)--Prilenia Therapeutics B.V., a clinical stage biotech company focused on developing novel treatments for neurodegenerative and neurodevelopmental disorders, today announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation to pridopidine for development as a potential treatment for Huntington’s Disease (HD).
NAARDEN, The Netherlands--(BUSINESS WIRE)--Prilenia Therapeutics B.V., a clinical stage biotech company focused on developing novel treatments for neurodegenerative and neurodevelopmental disorders, today announces the enrollment of the first participant for treatment with pridopidine in the pivotal HEALEY ALS Platform Trial.