Interventional {{label}}

Treatment Continuation Study for Patients With ALS/MND Who Completed Study CMD-2019-001

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 However, these sources may occasionally be outdated or inaccurate.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

Intervention or Drug Name

Sponsor

Trial Status

Phase

Randomization

Trial Duration

Route of Administration

Genetic Target

Repurposed Drugs

Approved by FDA

Approved outside USA

Is a supplement

Details

Enrollment Criteria

Time since symptom onset

Vital Capacity (FVC or SVC)

Approved Medications

Registry Listing

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Purpose

Provides up to six months treatment with CuATSM for subjects who have successfully completed study CMD-2019-001

What participation looks like

Provides up to six months treatment with CuATSM for subjects who have successffulyl completed study CMD-2019-001. [This allows subjects randomized to placebo on study CMD-2019-001 to receive up to six months treatment with CuATSM and provides an up to an additional six months treatment with CuATSM for subjects randomized to CuATSM on study CMD-2019-001]

Eligibility criteria

Inclusion Criteria:
- signed informed consent prior to initiation of any study-specific procedures and
treatment
- documented completion of protocol-specified assessments following completion of 24
weeks treatment on study CMD-2019-002
- Investigator considers patient has been tolerating treatment on study CMD-2019-001 and
may benefit from continued treatment with CuATSM
Exclusion Criteria:
- not dependent on mechanical ventilation

Locations

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Location Contact: {{location.Contact.Name}} {{location.Contact.Name}} Phone: {{location.Contact.Phone}}

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