A Phase IV Study to Evaluate Safety, Tolerability and Effectiveness of Rivastigmine Patch 15cm2 in Patients With Severe Dementia of the Alzheimer's Type.

  • STATUS
    Recruiting
  • End date
    Dec 30, 2022
  • participants needed
    102
  • sponsor
    Novartis Pharmaceuticals
Updated on 24 January 2022
dementia
alzheimer's disease
severe dementia
rivastigmine

Summary

This is a multicenter, prospective, phase IV study evaluating safety, tolerability and effectiveness of rivastigmine 27 mg -15 cm2 transdermal patch prescribed in patients with severe dementia of the Alzheimer's type as per discretion of treating physician.

Details
Condition Alzheimer's Disease
Treatment rivastigmine
Clinical Study IdentifierNCT02989402
SponsorNovartis Pharmaceuticals
Last Modified on24 January 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Patients willing to participate in the study by providing written informed consent
Patients diagnosed with severe dementia secondary to Alzheimer's disease (AD) 3 .Patient's prescribed with rivastigmine 27mg -15 cm2 transdermal patch as per discretion of treating physician

Exclusion Criteria

Contraindication as per PI
Patients simultaneously participating in other studies
Use of other investigational drugs within 5 half-lives of enrollment, or within 30 days (for small molecules) /until the expected PD effect has returned to baseline (for biologics)], whichever is longer
History of hypersensitivity to any of the study drugs or to drugs of similar chemical classes
Clear my responses

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Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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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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