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Development of an antisense oligonucleotide therapy for SOD1 Familial ALS

开发 SOD1 家族性 ALS 反义寡核苷酸疗法

基本信息

批准号：
8724083
负责人：
TIMOTHY M. MILLER
金额：
$ 28.85万
依托单位：
WASHINGTON UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2014
资助国家：
美国
起止时间：
2014-09-01 至 2017-08-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8724083
关键词：
Acute Adult Amyotrophic Lateral Sclerosis Animal Model Animals Antisense Oligonucleotide Therapy Antisense Oligonucleotides Antisense Technology Base Pairing Binding Biological Assay Blood - brain barrier anatomy Brain C9ORF72 Cerebrospinal Fluid Cessation of life Clinic Clinical Clinical Trials Data Development Disease Disease Progression Dose Drug Kinetics Enzymes Failure Familial Amyotrophic Lateral Sclerosis Generations Genetic Grant Human In Vitro Inborn Genetic Diseases Inflammatory Intrathecal Injections Knowledge Lead Leukocytes Link Liquid substance Macaca Mediating Messenger RNA Motor Neurons Mus Muscular Atrophy Mutation Nerve Degeneration Neuraxis Neurodegenerative Disorders Nuclear Onset of illness Organ Pharmaceutical Preparations Pharmacologic Substance Pharmacology Phase Probability Proteins Rattus Research Respiratory Muscles Rodent Safety Saline Secondary to Spinal Cord Syndrome Testing Tissues Toxic effect Toxicogenetics Toxicology Transcript Work base cohort effective therapy efficacy testing experience gain of function human study in vivo lateral ventricle mutant neuroprotection next generation nonhuman primate peripheral blood pre-clinical public health relevance ribonuclease H1 safety study superoxide dismutase 1 synthetic nucleic acid

项目摘要

DESCRIPTION (provided by applicant): Mutations in SOD1 cause approximately 2% of amyotrophic lateral sclerosis (ALS), an adult onset neurodegenerative disease characterized by loss of motor neurons resulting in severe weakness, muscle atrophy, and death typically in 3-5 years secondary to failure of respiratory muscles. Animal models and human studies suggest that lowering levels of SOD1 would be protective. We have developed antisense oligonucleotides that lower SOD1 in the brain and spinal cord when delivered to the cerebral spinal fluid. One of these antisense oligonucleotides was tested in a Phase I human clinical trial and demonstrated excellent safety at the low doses tested. However, it is clear from subsequent studies that we need to develop new antisense oligonucleotides for human SOD1. The collaborative work between Timothy Miller, Merit Cudkowicz and Isis Pharmaceuticals outlined in this grant will define a more potent, safer SOD1 antisense oligonucleotide by performing toxicology studies in rodents and non-human primates and by testing efficacy in the SOD1G93A rat studies. The successful completion of these studies will lead to an IND for the new SOD1 antisense oligonucleotide for SOD1-related ALS.

描述（由申请人提供）： SOD 1的突变导致约2%的肌萎缩侧索硬化症（ALS），这是一种成人发病的神经退行性疾病，其特征在于运动神经元的丧失，导致严重的虚弱、肌肉萎缩和死亡，通常在3-5年内继发于呼吸肌衰竭。动物模型和人体研究表明，降低SOD 1水平将具有保护作用。我们已经开发了反义寡核苷酸，当递送到脑脊髓液时，其降低脑和脊髓中的SOD 1。这些反义寡核苷酸之一在I期人类临床试验中进行了测试，并在测试的低剂量下表现出优异的安全性。然而，从随后的研究中可以清楚地看出，我们需要开发新的针对人SOD 1的反义寡核苷酸。Timothy米勒、Merit Cudkowicz和Isis Pharmaceuticals在此次资助中概述的合作工作将通过在啮齿动物和非人类灵长类动物中进行毒理学研究以及通过在SOD 1G 93 A大鼠研究中测试疗效来定义更有效、更安全的SOD 1反义寡核苷酸。这些研究的成功完成将导致新的SOD 1反义寡核苷酸用于SOD 1相关ALS的IND。