Arimoclomol at dosages up to 300 mg/day is well tolerated and safe in amyotrophic lateral sclerosis

被引:81
作者
Cudkowicz, Merit E. [1 ]
Shefner, Jeremy M. [2 ]
Simpson, Elizabeth [1 ]
Grasso, Daniela [1 ]
Yu, Hong [1 ]
Zhang, Hui [3 ]
Shui, Amy [3 ]
Schoenfeld, David [3 ]
Brown, Robert H. [4 ]
Wieland, Scott [5 ]
Barber, Jack R. [5 ]
机构
[1] Massachusetts Gen Hosp, Neurol Clin Trials Unit, Charlestown, MA 02129 USA
[2] SUNY Upstate Med Univ, Syracuse, NY USA
[3] Massachusetts Gen Hosp, Dept Biostat, Boston, MA 02114 USA
[4] Massachusetts Gen Hosp, Day Lab, Charlestown, MA 02129 USA
[5] CytRx Corp, Los Angeles, CA USA
关键词
amyotrophic lateral sclerosis; arimoclomol; clinical trial; protein aggregation;
D O I
10.1002/mus.21059
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Arimoclomol is an investigational drug for amyotrophic lateral sclerosis (ALS) that amplifies heat shock protein gene expression during cell stress. The objectives of the present study were to assess the safety, tolerability, and pharmacokinetics of arimoclomol in ALS. Eighty-four participants with ALS received arimoclomol at one of three oral doses (25, 50, or 100 ring three times daily) or placebo. The primary outcome measure was safety and tolerability. A subset of 44 participants provided serum and cerebrospinal fluid (CSF) samples for pharmacokinetic analysis. Participants who completed 12 weeks of treatment could enroll in a 6-month open-label study. Arimoclomol at doses up to 300 mg/day was well tolerated and safe. Arimoclomol resulted in dose-linear pharmacologic exposures and the half-life did not change with continued treatment. Arimoclomol CSF levels increased with dose. Arimoclomol was shown to be safe, and it crosses the blood-brain barrier. Serum pharmacokinetic profiles support dosing of three times per day. An efficacy study in ALS is planned.
引用
收藏
页码:837 / 844
页数:8
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