A randomized, double-blind, placebo-controlled trial of DaxibotulinumtoxinA for Injection for the treatment of upper limb spasticity in adults after stroke or traumatic brain injury.

IF 2.2 4区 医学 Q1 REHABILITATION PM&R Pub Date : 2024-10-01 DOI:10.1002/pmrj.13258
Atul T Patel, Michael C Munin, Ziyad Ayyoub, Gerard E Francisco, Rashid Kazerooni, Todd M Gross
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Abstract

Background: Intramuscular injection of botulinum toxin type A is a first-line pharmacotherapy for adults with upper limb spasticity (ULS). However, reemergence of symptoms within 12 weeks of treatment is common and longer-lasting treatments are needed.

Objective: To evaluate the efficacy and safety of three doses of DaxibotulinumtoxinA for Injection (DAXI) for treatment of ULS in adults with stroke or traumatic brain injury.

Intervention: Intramuscular injections of placebo (N = 24), DAXI 250 U (N = 22), DAXI 375 U (N = 19), or DAXI 500 U (N = 18) to the suprahypertonic muscle (SMG) and other muscle groups.

Design: Randomized, double-blind, placebo-controlled study.

Setting: Twenty-six study centers across the United States.

Participants: Eighty-three adult patients with ULS were randomly assigned to each treatment group and followed for up to 36 weeks.

Outcome measures: Co-primary endpoints were the Modified Ashworth Scale (MAS) score change from baseline in the designated SMG and Physician Global Impression of Change (PGIC) at Week 6.

Results: The mean changes from baseline in MAS score for the designated SMG for placebo and the DAXI 250 U, 375 U, and 500 U groups were -0.6, -0.9, -0.9, and -1.8, respectively, at Week 4 and -0.8, -0.9, -1.0, and -1.5, respectively, at Week 6. Statistically significant improvement in MAS score compared with placebo was reported only for the 500 U dose (Week 4: p < .001; Week 6: p = .049). Significant improvements in PGIC ratings compared with placebo were reported for DAXI 375 U (p = .015) and DAXI 500 U (p = .009) at Week 4 but not for any DAXI doses at Week 6. All DAXI doses were well tolerated with no trend toward more adverse events with increased dose.

Conclusion: Results from this Phase 2 study indicate that DAXI 500 U is effective and well tolerated for treatment of adults with ULS.

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注射用达希布妥毒素A治疗中风或脑外伤后成人上肢痉挛的随机、双盲、安慰剂对照试验。
背景:肌肉注射A型肉毒毒素是治疗成人上肢痉挛(ULS)的一线药物疗法。然而,治疗后 12 周内症状再次出现的情况很常见,因此需要更持久的治疗:目的:评估三种剂量的注射用达希布妥毒素 A(DAXI)治疗中风或脑外伤成人上肢痉挛的疗效和安全性:安慰剂(24 例)、DAXI 250 U(22 例)、DAXI 375 U(19 例)或 DAXI 500 U(18 例)肌肉注射到腱上肌(SMG)和其他肌群:随机、双盲、安慰剂对照研究:地点:全美 26 个研究中心:83名成年 ULS 患者被随机分配到每个治疗组,并接受长达 36 周的随访:共同主要终点是第6周时指定SMG的改良阿什沃斯量表(MAS)评分与基线相比的变化以及医生对变化的总体印象(PGIC):安慰剂组和DAXI 250 U、375 U和500 U组指定SMG的MAS评分与基线相比的平均变化分别为:第4周-0.6、-0.9、-0.9和-1.8;第6周-0.8、-0.9、-1.0和-1.5。与安慰剂相比,仅 500 U 剂量的 MAS 评分有统计学意义的改善(第 4 周:p 结论:与安慰剂相比,500 U 剂量的 MAS 评分有统计学意义的改善(第 6 周:p):这项 2 期研究的结果表明,DAXI 500 U 对成人 ULS 患者的治疗有效且耐受性良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
PM&R
PM&R REHABILITATION-SPORT SCIENCES
CiteScore
4.30
自引率
4.80%
发文量
187
审稿时长
4-8 weeks
期刊介绍: Topics covered include acute and chronic musculoskeletal disorders and pain, neurologic conditions involving the central and peripheral nervous systems, rehabilitation of impairments associated with disabilities in adults and children, and neurophysiology and electrodiagnosis. PM&R emphasizes principles of injury, function, and rehabilitation, and is designed to be relevant to practitioners and researchers in a variety of medical and surgical specialties and rehabilitation disciplines including allied health.
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