First clinical post-approval, observational study to assess clinical safety and effectiveness of brivaracetam sustained-release formulation in real-life settings of India: BEAM study

被引:0
作者
Ranganathan, Lakshmi Narasimhan [1 ]
Kulkarni, Girish [2 ]
Kakkad, Ashutosh [2 ]
Korukonda, Krishnaprasad [2 ]
Chouksey, Narendra [2 ]
机构
[1] Inst Neurol, Madras Med Coll, Chennai, Tamil Nadu, India
[2] Torrent Pharmaceut Ltd, Med Affairs, Off Ashram Rd, Ahmadabad, Gujarat, India
来源
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY | 2025年 / 125卷
关键词
Brivaracetam; Focal seizures; Real-world evidence; Sustained-release tablet; Effectiveness; Tolerability; PARTIAL-ONSET SEIZURES; EXTENDED-RELEASE; EFFICACY; EPILEPSY;
D O I
10.1016/j.seizure.2025.01.011
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose: Brivaracetam (BRV) sustained-release (SR) tablets have recently been approved to treat focal seizures in India. SR formulations enhance patient adherence and quality of life (QoL). We assessed safety and effectiveness of BRV-SR for epilepsy management in Indian real-life settings. Methods: A post-approval observational study involving 1989 patients receiving BRV-SR from 181 centres were analysed. Primary endpoints are efficacy variables derived from seizure-related changes, and secondary endpoints include responder rate (>= 50% reduction in focal-onset seizures [FoS]/focal-to-bilateral tonic-clonic seizures [FBTCS] frequency), usage pattern data, clinician's global impression on efficacy index (CGI-EI) and safety variables. Results: Patients' mean age was 42.33 +/- 12.33 years, and 1441 (72.44%) were men. Psychiatric comorbidities included depression (21.97%), sleep disturbance (15.54%), and anxiety (9.60%). The predominant seizure types were FoS (71.44%) and FBTCS (28.56%). BRV-SR 100 mg once-daily was most prescribed dose (57.37%) at baseline and follow-up visits (51.94%). Median seizure frequency decreased from 2 at baseline to 1 at follow-up visit. At follow-up, 72.1% patients were responders, and 63.75% were seizure-free. BRV-SR showed "marked" to "moderate" improvement in 92.99% of patients according to CGI-EI. Subgroup-analysis revealed a positive correlation between BRV-SR use in patients with drug-resistant epilepsy, psychiatric co-morbidities, and behavioural adverse events (AEs) with past anti-seizure medications. AEs were rare, with none reported in 97.39% patients during study period. Conclusion: The BEAM study findings provide first real-world evidence on effectiveness and safety of BRV-SR in Indian real-life settings. Furthermore, BRV-SR is a feasible option for focal epilepsy management with good retention rates and improved QoL.
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收藏
页码:132 / 139
页数:8
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