An Open-Label Study of ML-007C-MA in Adults With Alzheimer's Disease Psychosis

Recruiting Phase 2 Interventional Study
Psychosis Associated With Alzheimer's Disease
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About This Trial

ML-007C-MA-222 is a 52-week, flexible-dose, open-label extension study designed to evaluate the long-term safety, tolerability, and effectiveness of ML007C-MA in participants with ADP who have completed the antecedent study (ie, Study ML-007C-MA-221).

Trial Locations
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Eligibility Criteria
Inclusion Criteria 1. Willing and able to provide written informed consent, or, if deemed lacking in the capacity to provide informed consent, the following requirements for consent must be met: 1. The participant's LAR must provide written informed consent. AND 2. The participant will provi…
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+1 650 839 4380

ML-007C-MA-ADP@maplightrx.com

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