Safety and biomarker effects of solanezumab in patients with?Alzheimer¡¯s disease

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• 作者：Martin Farlow ; Steven E. Arnold ; Christopher H. van Dyck ; Paul S. Aisen ; B. Joy Snider ; Anton P. Porsteinsson ; Stuart Friedrich ; Robert A. Dean ; Celedon Gonzales ; Gopalan Sethuraman ; Ronald B. DeMattos ; Richard Mohs ; Steven M. Paul ; Eric R. Siemers
• 关键词：Alzheimer&rsquo ; s disease ; ¦Â-amyloid ; Cerebrospinal fluid immunotherapy ; A¦Â monoclonal antibody ; Solanezumab ; LY2062430
• 刊名：Alzheimer's Dementia
• 出版年：2012
• 出版时间：July, 2012
• 年：2012
• 卷：8
• 期：4
• 页码：261-271
• 全文大小：570 K

文摘

Objectives

To assess the safety, tolerability, pharmacokinetics, and pharmacodynamics of 12 weekly infusions of solanezumab, an anti-¦Â-amyloid (A¦Â) antibody, in patients with mild-to-moderate Alzheimer¡¯s disease. Cognitive measures were also obtained.

Methods

In this phase 2, randomized, double-blind, placebo-controlled clinical trial, 52 patients with Alzheimer¡¯s disease received placebo or antibody (100 mg every 4 weeks, 100 mg weekly, 400 mg every 4 weeks, or 400 mg weekly) for 12 weeks. Safety and biomarker evaluations continued until 1 year after randomization. Both magnetic resonance imaging and cerebrospinal fluid (CSF) examinations were conducted at baseline and after the active treatment period. The A¦Â concentrations were measured in plasma and CSF, and the Alzheimer¡¯s Disease Assessment Scale-cognitive portion was administered.

Results

Clinical laboratory values, CSF cell counts, and magnetic resonance imaging scans were unchanged by treatment, and no adverse events could be clearly related to antibody administration. Total (bound to antibody and unbound) A¦Â_1-40 and A¦Â_1-42 in plasma increased in a dose-dependent manner. Antibody treatment similarly increased total A¦Â_1-40 and A¦Â_1-42 in CSF. For patients taking 400 mg weekly, antibody treatment decreased unbound A¦Â_1-40 in CSF (P < .01), but increased unbound A¦Â_1-42 in CSF in a dose-dependent manner. The Alzheimer¡¯s Disease Assessment Scale-cognitive portion was unchanged after the 12-week antibody administration.

Conclusions

Antibody administration was well tolerated with doses up to 400 mg weekly. The dose-dependent increase in unbound CSF A¦Â_1-42 suggests that this antibody may shift A¦Â equilibria sufficiently to mobilize A¦Â_1-42 from amyloid plaques.