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

  • End date
    Dec 30, 2021
  • participants needed
  • sponsor
    Collaborative Medicinal Development Pty Limited
Updated on 24 January 2021


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


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]

Condition Myelopathy, Amyotrophic Lateral Sclerosis, Amyotrophic Lateral Sclerosis (ALS), Spinal Cord Disorders, lou gehrig's disease
Treatment Cu(II)ATSM
Clinical Study IdentifierNCT04313166
SponsorCollaborative Medicinal Development Pty Limited
Last Modified on24 January 2021


Yes No Not Sure

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
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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