A Prospective, Non-Interventional, Observational, Multicenter Study to Investigate Dosage, Effectiveness, and Safety of Perampanel When Used as First Adjunctive Therapy in the Routine Clinical Care of Subjects >=12 Years With Partial Onset Seizures With or Without Secondary Generalization or With Primary Generalized Tonic-Clonic Seizures Associated With Idiopathic Generalized Epilepsy

13/07/2023
23/04/2024
EU PAS number:
EUPAS105866
Study
Finalised
Documents
Study protocol
Study results
Study results
English (384.7 KB - PDF) View document
Study report
Other information