Severe Alzheimer/Dementia Study -DUS44 Clinical Trial Information

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Severe Alzheimer/Dementia Study -DUS44

The purpose of this 24 week, prospective, randomized, parallel-group, double-blind, multi-center study is to compare the effects of two different doses of a Novartis investigational drug in people with severe dementia/Alzheimers. An "investigational drug" is a drug that is being clinically tested and is not approved for sale or use in the United States by the Food and Drug Administration (FDA), for the indication in which it is being studied.
Trial phase: Phase 4
Participation Duration: The participant will be required to visit the doctor’s office 6 times over about 28 weeks.
Protocol Number: CENA713DUS44

The next step is to see if you (or the participant) meet the basic criteria required for participation in this clinical trial. Please fill out the questionnaire below to see if you (or the participant) may be suitable for the clinical trial. Your answers to these questions are not retained by this system. You must answer the questions below for yourself, or, you must be the legally authorized representative of the potential participant in order to answer the questions on their behalf. If you (or the participant) do not meet the preliminary qualifications, you may search for other clinical trials of interest or sign up to the Mailing List.

Answers to all questions are required to determine if you meet the preliminary qualifications for the study.

1) Participation in a clinical trial will require travel to a study center where the clinical trial is being conducted. How far would you (or the participant) be willing to travel to a study center to participate in this clinical trial? Please note that participation in these clinical trials may require a number of visits to the study center and travel expenses may not be covered.

25 miles 50 miles 100 miles 150 miles Unlimited

2) Please enter your residential postal zip code.

3) Are you (or the participant) at least 50 years of age?
Yes
No

4) Have you (or the participant) been diagnosed with severe Alzheimer’s disease dementia?
Yes
No

5) Will you (or the participant) be able to visit the study center for each appointment? Please note that visits to nursing centers or outside facilities are not available.
Yes
No

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