Safety and tolerability of adjunctive brivaracetam in epilepsy: In-depth pooled analysis

Abstract

Objective: The objective of this analysis was to provide a comprehensive analysis of safety data for adjunctive brivaracetam (BRV), an antiepileptic drug (AED) of the racetam class, for treatment of focal seizures in patients with epilepsy.

Methods: Data were pooled from two phase II, placebo-controlled, double-blind, dose-ranging trials (N01114 [ClinicalTrials.gov: NCT00175929], N01193 [NCT00175825]) and three phase III, placebo-controlled, double-blind, 12-week trials (N01252 [NCT00490035], N01253 [NCT00464269], and N01358 [NCT01261325]) in patients aged ≥16 years with focal seizures, as well as a phase III, placebo-controlled, double-blind, 16-week trial in patients aged ≥16 years with focal or generalized epilepsy (N01254 [NCT00504881]). Data are presented for the approved therapeutic dose range of 50-200 mg/day. Data for BRV administered intravenously (25-150 mg doses) were pooled separately from one phase III trial (N01258 NCT01405508]) and two clinical pharmacology trials (N01256 [Part B] [UCB Pharma, data on file]; EP0007 [NCT01796899]). Adverse events (AEs) of interest were summarized in relevant categories.

Results: The safety pool comprised 1957 patients: 1271 receiving adjunctive BRV and 686 receiving placebo. Overall, the incidence of treatment-emergent adverse events (TEAEs) was 66.9% with BRV versus 62.8% with placebo. The most frequently reported TEAEs with BRV (≥5% of patients) versus placebo were somnolence (13.3% vs. 7.9%), headache (10.5% vs. 11.5%), dizziness (10.0% vs. 7.0%), and fatigue (8.2% vs. 4.2%). Incidence of psychiatric disorder-related TEAEs was 11.3% with BRV versus 8.2% with placebo. Behavioral disorder-related TEAE incidence was low (4.0% with BRV vs. 2.5% with placebo). Irritability was reported in 2.7% of BRV-treated patients vs. 1.5% of patients receiving placebo; anger, aggression, and agitation were each reported by ≤1% of patients receiving BRV. Treatment-emergent adverse events potentially associated with psychosis were psychotic disorder (three patients on BRV vs. two patients on placebo), auditory hallucination, illusion, visual hallucination (one patient each on BRV), epileptic psychosis, and hallucination (one patient each on placebo). No additional safety concerns were identified in patients with intravenous (IV) BRV administration (n = 104).

Conclusions: These safety data for adjunctive BRV support its acceptable safety and tolerability profile.

Keywords: Adjunctive; Antiepileptic drug; Brivaracetam; Epilepsy; Safety; Tolerability.

Conflict of interest statement

Declaration of competing interest Christian Brandt reports personal compensation from Actelion/Idorsia, Arvelle, Desitin, Eisai, GW Pharmaceuticals, Novartis, Pfizer, SKS, UCB Pharma, and USL Pharma for serving on a scientific advisory board, for speaking activities, or congress travel. Pavel Klein reports being a consultant for Alliance, Eisai, Lundbeck, SK Life Science, Sunovion, and UCB Pharma; being on the speakers bureau for Eisai, Sunovion, and UCB Pharma; and receiving grant support from Eisai and Lundbeck. Vincent Badalamenti is a former employee of UCB Pharma. Teresa Gasalla and John Whitesides are employees of UCB Pharma.

Copyright © 2019. Published by Elsevier Inc.