Safety and Efficacy of Piromelatine in Mild Alzheimer's Disease Patients (ReCOGNITION)
Status: | Active, not recruiting |
---|---|
Conditions: | Alzheimer Disease |
Therapuetic Areas: | Neurology |
Healthy: | No |
Age Range: | 60 - 85 |
Updated: | 3/23/2019 |
Start Date: | November 2015 |
End Date: | April 2019 |
Randomized, Double-blind, Parallel-group, Placebo-controlled, Dose Ranging Study of Piromelatine in Patients With Mild Dementia Due to Alzheimer's Disease
This study is a Phase 2, randomized, placebo controlled, dose ranging study of piromelatine
(5, 20, and 50 mg daily for 6 months) versus placebo to determine an effective dose based on
efficacy (cognitive performance), safety and tolerability in patients with mild dementia due
to AD.
(5, 20, and 50 mg daily for 6 months) versus placebo to determine an effective dose based on
efficacy (cognitive performance), safety and tolerability in patients with mild dementia due
to AD.
Inclusion Criteria:
- Patient and caregiver are willing to take part in the entire study
- Signed informed consent from the patient and the caregiver
- Patient has a clearly documented history either in medical records or from an
informant of cognitive decline over at least 6 months
- Patient has mild probable AD as consistent with criteria established by the NIA-AA
- CT/MRI scan with finding consisted with probable AD obtained during the last 12 months
before Screening
- Patient has an MMSE score of 21-26 (inclusive) at Screening
- Patient has a Clinical Dementia Rating Global Score (CDR-GS) of 0.5-1 (mild dementia)
at Screening
- Patients receiving prescribed drugs for treatment of AD including acetyl
cholinesterase inhibitors [eg, donepezil, galantamine, rivastigmine] should be on a
stable dose for at least 3 months before Screening
- Patient has a negative drug screen (benzodiazepines or opiates) at Screening
- Female patients must have had last natural menstruation ≥ 24 months before Screening,
OR be surgically sterile
- Male patients must agree to use of effective contraception if female partner is of
childbearing potential, OR be surgically sterile
Exclusion Criteria:
- Patient has an alternative cause for dementia other than AD as determined by CT or MRI
scan
- Patient has evidence of any clinically significant neurodegenerative disease
- Patient has been diagnosed with the following Axis I disorders (DSM V criteria)
- Patient has a history of uncontrolled or untreated cardiovascular, endocrine,
gastrointestinal, respiratory, or rheumatologic disorders within the past 5 years
- Patient has severe pain that is likely to interfere with sleep
- Continuous use of benzodiazepines or other sedative-hypnotics during the 2 weeks
before Screening
- Use of any kind of melatonin/melatonin agonist during the 2 weeks before Screening
- Patient has known or suspected hypersensitivity to exogenous melatonin or melatonin
receptor agonists
- Patients with an irregular lifestyle or life pattern (eg, shift workers, patients
likely to be jet lagged).
We found this trial at
56
sites
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1720 2nd Ave S
Birmingham, Alabama 35233
Birmingham, Alabama 35233
(205) 934-4011
Phone: 205-934-1821
University of Alabama at Birmingham The University of Alabama at Birmingham (UAB) traces its roots...
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Ohio State University The Ohio State University’s main Columbus campus is one of America’s largest...
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