Lynch David R, Chin Melanie P, Boesch Sylvia, Delatycki Martin B, Giunti Paola, Goldsberry Angie, Hoyle J Chad, Mariotti Caterina, Mathews Katherine D, Nachbauer Wolfgang, O'Grady Megan, Perlman Susan, Subramony S H, Wilmot George, Zesiewicz Theresa, Meyer Colin J
Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Reata Pharmaceuticals, Dallas, Texas, USA.
Mov Disord. 2023 Feb;38(2):313-320. doi: 10.1002/mds.29286. Epub 2022 Nov 29.
MOXIe was a two-part study evaluating the safety and efficacy of omaveloxolone in patients with Friedreich's ataxia, a rare, progressive neurological disease with no proven therapy. MOXIe part 2, a randomized double-blind placebo-controlled trial, showed omaveloxolone significantly improved modified Friedreich's Ataxia Rating Scale (mFARS) scores relative to placebo. Patients who completed part 1 or 2 were eligible to receive omaveloxolone in an open-label extension study.
The delayed-start study compared mFARS scores at the end of MOXIe part 2 with those at 72 weeks in the open-label extension period (up to 144 weeks) for patients initially randomized to omaveloxolone versus those initially randomized to placebo.
We performed a noninferiority test to compare the difference between treatment groups (placebo to omaveloxolone versus omaveloxolone to omaveloxolone) using a single mixed model repeated measures (MMRM) model. In addition, slopes of the change in mFARS scores were compared between both groups in the open-label extension.
The noninferiority testing demonstrated that the difference in mFARS between omaveloxolone and placebo observed at the end of placebo-controlled MOXIe part 2 (-2.17 ± 1.09 points) was preserved after 72 weeks in the extension (-2.91 ± 1.44 points). In addition, patients previously randomized to omaveloxolone in MOXIe part 2 continued to show no worsening in mFARS relative to their extension baseline through 144 weeks.
These results support the positive results of MOXIe part 2 and indicate a persistent benefit of omaveloxolone treatment on disease course in Friedreich's ataxia. © 2022 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
MOXIe研究分为两个部分,旨在评估奥伐洛酮对弗里德赖希共济失调患者的安全性和有效性。弗里德赖希共济失调是一种罕见的进行性神经疾病,尚无经证实有效的治疗方法。MOXIe研究的第二部分是一项随机双盲安慰剂对照试验,结果显示,与安慰剂相比,奥伐洛酮显著改善了改良弗里德赖希共济失调评定量表(mFARS)评分。完成第一部分或第二部分研究的患者有资格在一项开放标签扩展研究中接受奥伐洛酮治疗。
这项延迟启动研究比较了最初随机分配接受奥伐洛酮治疗的患者与最初随机分配接受安慰剂治疗的患者在MOXIe研究第二部分结束时与开放标签延长期(长达144周)72周时的mFARS评分。
我们使用单一混合模型重复测量(MMRM)模型进行非劣效性检验,以比较治疗组之间的差异(安慰剂组与奥伐洛酮组对比奥伐洛酮组与奥伐洛酮组)。此外,在开放标签延长期比较了两组mFARS评分变化的斜率。
非劣效性检验表明,在安慰剂对照的MOXIe研究第二部分结束时观察到的奥伐洛酮与安慰剂之间的mFARS差异(-2.17±1.09分)在延长期72周后得以保持(-2.91±1.44分)。此外,在MOXIe研究第二部分中先前随机分配接受奥伐洛酮治疗的患者在长达144周的时间里相对于其延长期基线,mFARS评分持续显示无恶化。
这些结果支持了MOXIe研究第二部分的阳性结果,并表明奥伐洛酮治疗对弗里德赖希共济失调病程具有持续益处。©2022作者。《运动障碍》由Wiley Periodicals LLC代表国际帕金森和运动障碍协会出版。