
Current Studies
BIIB067 When Initiated in Clinically Presymptomatic Adults With a Confirmed Superoxide Dismutase 1 Mutation
This study first aims to evaluate the efficacy of BIIB067 when initiated in presymptomatic adult carriers of a superoxide dismutase 1 (SOD1) mutation with elevated neurofilament (NF). It also aims are to evaluate the safety and tolerability of BIIB067 and to evaluate the effect of BIIB067 on pharmacodynamics (PD)/treatment response biomarkers when initiated prior to versus at the time of emergence of clinically manifest amyotrophic lateral sclerosis (ALS).
Key inclusion criteria
Aged 18 years or older at the time of enrollment
Participants should have a protocol-defined rapidly progressive SOD1 mutation
Participants with plasma NfL level less than the protocol-defined threshold
Participants who are clinically presymptomatic for ALS
Key exclusion criteria
History or positive test result at screening for human immunodeficiency virus (HIV)
Current hepatitis C infection. Participants with positive HCV antibody and undetectable HCV Ribonucleic Acid (RNA) are eligible to participate in the study
Current hepatitis B infection. Participants with immunity to hepatitis B from previous natural infection or vaccination are eligible to participate in the study
History of systemic hypersensitivity reaction to tofersen, the excipients contained in the formulation, and if appropriate, any diagnostic agents to be administered during the study
History of confounding neuromuscular or neurological disorder that is expected to have a progressive course during the study, and/or is expected to be associated with elevations in NF
Presence of risk for increased or uncontrolled bleeding and/or risk of bleeding that if not managed optimally could place a participant at an increased risk for intraoperative or postoperative bleeding
Significant cognitive impairment, clinical dementia, or unstable psychiatric illness, including psychosis, suicidal ideation, suicide attempt, or untreated major depression ≤ 90 days of screening
Treatment with riluzole and/or edaravone. If the participant has been on riluzole and/or edaravone, the medication(s) must be discontinued for at least 5 half-lives prior to screening.
Use of off-label treatments for ALS
Treatment with another investigational drug, biological agent, or device within 1 month or 5 half-lives of study agent, whichever is longer. Specifically, no prior treatment with small interfering RNA, stem cell therapy, or gene therapy is allowed
Anticipated need, in the opinion of the Investigator, for administration of any antiplatelet or anticoagulant medication that cannot be safely continued or held for an LP procedure, if necessary, according to local or institutional guidelines and/or Investigator determination
Current enrollment or a plan to enroll in any interventional clinical study in which an investigational treatment, biological agent, device, or approved therapy for investigational use. Participation in a noninterventional study focused on ALS natural history may be allowed
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Multiple sclerosis (MS) is a disease entity with several distinct clinical phenotypes where progression can be gradual and subtle. As a result, the clinical tools designed to help clinicians monitor overall disease progression may not be sensitive enough to detect early changes in cognitive status before these changes become more disabling. MS is also characterized by subtle anomalous eye movements and a growing body of evidence has suggested that these impairments could be related to both disease severity and cognition.