达福普定缓释改善多发性硬化症患者行走速度的症状。

Core Evidence Pub Date : 2010-01-01 Epub Date: 2010-12-08 DOI:10.2147/CE.S9046
Douglas R Jeffery, Emily Poole Pharr
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引用次数: 8

摘要

Dalfampridine缓释(SR)是一种4-氨基吡啶的缓释制剂,最近被美国食品和药物管理局批准用于改善多发性硬化症(MS)患者的行走。在II期试验中,MS患者的步行速度和下肢肌肉力量增加,但步行速度的增加没有达到统计学意义。一项应答分析显示,大约35%的治疗患者的步行速度有统计学意义和临床意义的增加。当治疗反应组与治疗无反应组比较时,反应组的步行速度显著增加,而无反应组或安慰剂组则没有。这一结果在两个更大的III期试验中得到了重复。使风险-收益比最大化的最佳剂量为10mg,每日两次。较高的剂量与更大的癫痫发作风险相关,但在步行速度或反应者比例方面没有进一步改善。darfampridine SR通过肾脏清除率排出,只进行有限的代谢(
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Dalfampridine sustained-release for symptomatic improvement of walking speed in patients with multiple sclerosis.

Dalfampridine sustained-release (SR) is a time-release formulation of 4-aminopyridine, recently approved by the Food and Drug Administration to improve walking in patients with multiple sclerosis (MS). In Phase II trials, walking speed and lower extremity muscle strength was increased in patients with MS, but the increase in walking speed did not reach statistical significance. A responder analysis revealed that approximately 35% of treated patients had a statistically significant and clinically meaningful increase in walking speed. When treated responders were compared with treated nonresponders, walking speed significantly increased in the responder group, but not in the nonresponder or placebo groups. This result was duplicated in two larger Phase III trials. The optimal dose to maximize the risk-benefit ratio was 10 mg twice daily. Higher doses were associated with a greater risk of seizure, but no further improvement in walking speed or in the proportion of responders. Dalfampridine SR is eliminated by renal clearance and undergoes only limited metabolism (<10%). It is contraindicated in patients with moderate or severe renal insufficiency and in those with a history of seizures or epileptiform activity on electroencephalography. The development of time-released 4-aminopyridine represents a major advance in symptomatic therapy for MS.

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Core Evidence
Core Evidence PHARMACOLOGY & PHARMACY-
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期刊介绍: Core Evidence evaluates the evidence underlying the potential place in therapy of drugs throughout their development lifecycle from preclinical to postlaunch. The focus of each review is to evaluate the case for a new drug or class in outcome terms in specific indications and patient groups The emerging evidence on new drugs is reviewed at key stages of development and evaluated against unmet needs
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