» Articles » PMID: 24094693

Safety and Tolerability of Different Titration Rates of Retigabine (ezogabine) in Patients with Partial-onset Seizures

Overview
Journal Epilepsy Res
Specialty Neurology
Date 2013 Oct 8
PMID 24094693
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

Retigabine (RTG; international nonproprietary name)/ezogabine (EZG; US adopted name) is an antiepileptic drug (AED) that prolongs neuronal voltage-gated potassium-channel KCNQ2-5 (Kv 7.2-7.5) opening. This double-blind study evaluated different RTG/EZG dose-titration rates. Patients (N=73) with partial-onset seizures receiving concomitant AEDs were randomized to one of three titration groups, all of which were initiated at RTG/EZG 300mg/day divided into three equal doses. Fast-, medium-, and slow-titration groups received dose increments of 150mg/day every 2, 4, and 7 days, respectively, achieving the target dose of 1200mg/day after 13, 25, and 43 days, respectively. Safety assessments were performed throughout. Discontinuation rates due to treatment-emergent adverse events (TEAEs) were numerically higher in the fast- (10/23) and medium- (7/22) titration groups than in the slow-titration group (3/23) but statistical significance was achieved only for the high-titration group compared with the low-titration group (p=0.024). Stratified analysis, with concomitant AEDs divided into enzyme inducers (carbamazepine, phenytoin, oxcarbazepine) or noninducers, showed that the risk of discontinuation due primarily to TEAEs was significantly higher in the fast- (p=0.010) but not in the medium-titration group (p=0.078) when compared with the slow-titration group. Overall, the slow-titration rate appeared to be best tolerated and was used in further efficacy and safety studies with RTG/EZG.

Citing Articles

The art and science of drug titration.

Caffrey A, Borrelli E Ther Adv Drug Saf. 2021; 11:2042098620958910.

PMID: 33796256 PMC: 7967860. DOI: 10.1177/2042098620958910.


Impact of antiepileptic-drug treatment burden on health-care-resource utilization and costs.

Rajagopalan K, Candrilli S, Ajmera M Clinicoecon Outcomes Res. 2018; 10:619-627.

PMID: 30425541 PMC: 6201987. DOI: 10.2147/CEOR.S180913.


Practice guideline update summary: Efficacy and tolerability of the new antiepileptic drugs II: Treatment-resistant epilepsy: Report of the American Epilepsy Society and the Guideline Development, Dissemination, and Implementation Subcommittee of....

Kanner A, Ashman E, Gloss D, Harden C, Bourgeois B, Bautista J Epilepsy Curr. 2018; 18(4):269-278.

PMID: 30254528 PMC: 6145395. DOI: 10.5698/1535-7597.18.4.269.


Antiepileptic drugs in development pipeline: A recent update.

Kaur H, Kumar B, Medhi B eNeurologicalSci. 2018; 4:42-51.

PMID: 29430548 PMC: 5803110. DOI: 10.1016/j.ensci.2016.06.003.


Tolerability of new antiepileptic drugs: a network meta-analysis.

Zaccara G, Giovannelli F, Giorgi F, Franco V, Gasparini S, Benedetto U Eur J Clin Pharmacol. 2017; 73(7):811-817.

PMID: 28378057 DOI: 10.1007/s00228-017-2245-z.