作者
Leonard H. van den Berg,Jeffrey D. Rothstein,Pamela J. Shaw,Suma Babu,Michael Benatar,Robert C. Bucelli,Angela Genge,Jonathan D. Glass,Orla Hardiman,Vincenzo Libri,Theodore Mobach,Björn Oskarsson,Gary L. Pattee,John Ravits,Christopher E. Shaw,Markus Weber,Lorne Zinman,Paymaan Jafar‐Nejad,Frank Rigo,Luan Lin,Toby A. Ferguson,Anthony L. Gotter,Danielle Graham,Michael Monine,Jennifer Inra,Susie Sinks,Satish A. Eraly,Steve Garafalo,Stephanie Fradette
摘要
Hexanucleotide repeat expansion of C9orf72 is a common genetic cause of amyotrophic lateral sclerosis (ALS). No C9orf72-targeted treatments are available. BIIB078 is an investigational antisense oligonucleotide targeting C9orf72 sense RNA. We aimed to assess the safety, tolerability, and pharmacokinetics of BIIB078 in participants with C9orf72-associated ALS.