EC approval for Ontozry : vimarsana.com

EC approval for Ontozry


EC approval for Ontozry
Angelini Pharma has announced European Commission (EC) approval for anti-seizure drug Ontozry (cenobamate).
The move allows doctors to prescribe the drug for the adjunctive treatment of focal-onset seizures with or without secondary generalisation in adults who have not been adequately controlled despite a history of treatment with at least two anti-epileptic medicines.
The EC marketing authorisation is valid in all European Union (EU) member states plus Iceland, Norway and Liechtenstein; the UK's Medicines and Healthcare Regulatory Agency (MHRA) is currently reviewing the submission for the drug via the reliance route*.
People with epilepsy whose seizures are poorly controlled have “higher morbidity and mortality rates and often experience comorbid illnesses, social stigmatisation and an impaired quality of life,” the company notes, highlighting the existing unmet need for such patients.

Related Keywords

Norway , Iceland , Liechtenstein , United Kingdom , Angelini Pharma , Agnese Cattaneo , Pierluigi Antonelli , European Commission Decision Reliance Procedure , European Union , European Commission , European Medicine Agency , Healthcare Regulatory Agency , Seizure , Epilepsy , Ontozry , Cenobamate , Angelini , நோர்வே , ஐஸ்லாந்து , லிக்டந்ஸ்டைந் , ஒன்றுபட்டது கிஂக்டம் , ஏஞ்சலினி பார்மா , ஐரோப்பிய தரகு முடிவு நம்பகத்தன்மை ப்ரொஸீஜர் , ஐரோப்பிய தொழிற்சங்கம் , ஐரோப்பிய தரகு , வலிப்பு , கால் கை வலிப்பு , ஏஞ்சலினி ,

© 2025 Vimarsana