Observational {{label}}

Rehabilitation in SOD1 ALS Treated With Tofersen

Please note: All trial information reflects the latest data available from the sponsor on ClinicalTrials.gov and other public databases. However, these sources may occasionally be outdated or inaccurate. For the most current information, we recommend contacting the trial sponsor or sites directly.

Overview

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Approved by FDA
Approved outside USA
Is a supplement

Details

Enrollment Criteria

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The primary objective of this study is to document and describe the effects of a personalized rehabilitation program for patients with SOD1 ALS participating in the tofersen expanded access program. Participants currently receiving tofersen treatment will be referred to outpatient physical and/or occupational therapy. Participants will have an initial assessment performed and an individualized rehabilitation program will be prescribed. Each participant is encouraged to follow the prescribed recommendations that will include scheduled outpatient therapy sessions, functional assessments, and/or a home-based rehabilitation program. Functional assessments will be done at a minimum of every three months.

Inclusion Criteria:
- Confirmed diagnosis of ALS with an SOD1 mutation
- Current enrollment in the tofersen expanded access program
- Age greater than 18 years
- Medically able to participate in outpatient physical therapy and/or home-based
rehabilitation, as determined by the treating health care provider
Exclusion Criteria:
- Any comorbidities or conditions that, in the opinion of the treating healthcare
provider, would unacceptably increase the risk of participation in outpatient physical
therapy and/or home-based rehabilitation

Locations
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Mitsubishi Tanabe Pharma