BRIVIACT (brivaracetam) by UCB Pharma is epoxide hydrolase inhibitors [moa]. First approved in 2016.
Drug data last refreshed 1h ago · AI intelligence enriched 6d ago
Briviact (brivaracetam) is a small-molecule antiepileptic agent approved by the FDA in 2016 as an adjunctive treatment for partial-onset seizures. It works via selective binding to synaptic vesicle protein 2A (SV2A), distinct from traditional GABAergic mechanisms. The drug is administered intravenously and represents an alternative mechanism in the competitive seizure management landscape.
Post-LOE lifecycle indicates a maturing product with likely smaller commercial teams and focus on lifecycle management rather than growth expansion.
Epoxide Hydrolase Inhibitors
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
A Study to Test the Long-term Safety and Tolerability of Brivaracetam in Study Participants With Childhood Absence Epilepsy or Juvenile Absence Epilepsy
A Study to Assess the Bioequivalence Between Brivaracetam Tablet and Dry Syrup in Healthy Japanese Male Study Participants
A Study to Assess the Bioequivalence Between Brivaracetam Tablet and Dry Syrup in Healthy Male Japanese Study Participants
A Study to Test the Long-term Safety, Tolerability and Efficacy of Brivaracetam in Study Participants 2 to 26 Years of Age With Childhood Absence Epilepsy or Juvenile Absence Epilepsy
A Study to Evaluate the Efficacy, Safety, and Tolerability of Brivaracetam as Monotherapy in Patients 2 to 25 Years of Age With Childhood Absence Epilepsy or Juvenile Absence Epilepsy
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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Working on Briviact offers limited career growth prospects given its post-LOE status and imminent generic entry in 2026. Career trajectories are best suited for professionals seeking stability in a mature product management role or those building LOE transition and lifecycle management expertise.