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Rasagiline Rescue in Alzheimer's Disease Clinical Trial

A 24-week, Three-site, Randomized, Double Blind, Placebo Controlled, Parallel Group, Proof-of-concept Study to Evaluate Rasagiline in the Regional Brain Metabolism on FDG PET in Patients With Mild to Moderate Alzheimer's Disease

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02359552
Acronym
R2
Enrollment
50
Registered
2015-02-10
Start date
2015-05-31
Completion date
2019-01-04
Last updated
2020-11-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer's Disease

Brief summary

This is a Phase II, randomized, double blind, placebo controlled, parallel group, proof of concept three-site study, to evaluate the effect of Rasagiline in the regional brain metabolism on 18F-2-fluoro-2-deoxy-D-glucose fluorodeoxyglucose (FDG-PET).

Detailed description

The study consists of two phases: a 24 week double blind placebo controlled treatment period and a 4 week follow up period. Patients will be randomized in a 1: 1 ratio at baseline to receive either Rasagiline or matching placebo The study drug will be given as 0.5 mg dose once daily for the 4 weeks, then increases to 1 mg daily for the next 20 weeks. A total of 50 subjects will be enrolled: 25 will receive Rasagiline and 25 will receive matching placebo for the 24-week treatment period. Primary objective is to determine if exposure to 1 mg of Rasagiline daily is associated with improved regional brain metabolism in the treatment group compared to the placebo group in Alzheimer's Disease patients

Interventions

DRUGRasagiline
DRUGPlacebo

Sponsors

The Cleveland Clinic
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
50 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Males or females 50 to 90 of age inclusive. * Diagnosis of probable AD (NINCDS-ADRDA criteria) * Positive fluoro-deoxyglucose PET (\[18F\]-FDG PET) scan compatible with AD as determined by the ADM Diagnostics LLC (ADMdx) Criteria at screening * Mini Mental Status Exam = 12 - 22 (inclusive) * Must have a study partner who is able and willing to comply with all required study procedures. * Have at least eight years of education and should have previously (in pre-AD condition) been capable of reading, writing, and communicating effectively with others in English. * If receiving therapy with a cholinesterase inhibitor and/or memantine, the dose of these agents has been stable for at least 3 months prior to screening

Exclusion criteria

* Any non-AD neurological disease * MRI findings indication of a non-AD diagnosis * Screening laboratory studies that are 1.5 times above or below the highest and lowest range of normal for each test respectively * History of melanoma; history of malignancy within the past five years with the exception of basal cell or squamous cell cancer, in-situ cervical cancer, or localized prostate cancer

Design outcomes

Primary

MeasureTime frameDescription
Change in Regional Glucose Metabolism Between Week 24 and Baseline as Measured by 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography (FDG-PET).24 weeksThe primary outcome measure is the change from baseline to week 24 in FDG-PET as measured by Standard Uptake Units Regional (SUVR) in several pre-specified brain regions including the medial temporal, lateral temporal, posterior cingulate - precuneus, inferior parietal, middle frontal, anterior cingulate, and striatum. The SUVR change was calculated by subtracting the value at 24 weeks from baseline values. Negative values indicate increased hypometabolism (i.e. worsening of cell function).

Secondary

MeasureTime frameDescription
Change in MMSE (Mini Mental Status Examination) ScoreMean change in scores from baseline to week 24Measure Description: The MMSE (Mini Mental Status Examination) is a brief, frequently used screening instrument for AD drug studies. The MMSE evaluates orientation, memory, attention, concentration, naming, repetition, comprehension, and ability to create a sentence and to copy two overlapping pentagons. A lower score indicates more cognitive impairment. The highest score is 30, range is between 0 (severe impairment) and 30 (cognitively normal). We calculated the change in scores by subtracting week 24 score from baseline. A negative score indicates clinical worsening.
Change in ADCS-ADL (Alzheimer's Disease Cooperative Study-Activities of Daily Living) ScoreMean change in scores from baseline to week 24Measure Description: The ADCS-ADL (Alzheimer's Disease Cooperative Study-Activities of Daily Living) is an activities-of-daily-living inventory developed by the ADCS to assess functional performance in participants with AD. Using a structured interview format, study partners are queried as to whether participants attempted each item in the inventory during the past 4 weeks and their level of performance. The ADCS-ADL provides a total score from 0-78, with a lower score indicating greater severity. We calculated change by subtracting scores on week 24 test from the baseline score. A negative score indicates worsening ability to complete ADLs.
Change in NPI (Neuropsychiatric Inventory) ScoreMean change in scores from baseline to week 24Measure Description: The behavioral outcome measure for this trial is the NPI (Neuropsychiatric Inventory). The NPI evaluates both the frequency and severity of 10 neuropsychiatric disturbances. Frequency assessments range from 1 (occasionally, less than once per week) to 4 (very frequently, once or more per day or continuously) as well as severity (1=mild, 2=moderate, 3=severe). The overall score is calculated by summing the severity and frequency of the subscale measures. The range of scores is 0-40. A score of 0 indicates no behavioral impairment and a score of 40 indicates severe behavioral impairment. We calculated change by subtracting Week 24 scores from baseline scores. A positive change indicates behavioral worsening.
Change in ADAS-Cog 11 (Alzheimer's Disease Assessment Scale - Cognitive 11) ScoreMean change in scores from baseline to week 24The ADAS-Cog 11 (Alzheimer's Disease Assessment Scale - Cognitive 11) is a psychometric instrument that evaluates memory, attention, reasoning, language, orientation, and praxis. A higher score indicates more impairment. Scores from the original portion of the test range from 0 (best) to 70 (worse). We used total ADAS-Cog 11 scores, which is a sum of individual subscales. We calculated the change by subtracting the ADAS Cog score at week 24 from baseline score. A positive change indicates cognitive worsening.
Change in COWAT (Controlled Oral Word Association Test) ScoreMean change in scores from baseline to week 24Measure Description: Study participants are instructed, I want to see how many words you can say beginning with a certain letter in one minute. The study participant's responses are recorded on the worksheet. Study participants are then given an additional one minute for each of two different letters using similar instructions. The score is the total number of acceptable words for the three trials combined. A higher score represents better performance. Responses are then judged for their acceptability (example for the use of proper nouns, numbers, repetitions and stem word with a different ending). The score is the total number of acceptable words for the three trials combined. A higher score represents better performance. We calculated change by subtracting week 24 scores from baseline scores. A negative score indicates worse performance.
Change in QoL-AD (Quality of Life - Alzheimer's Disease) ScoreThis assessment will be performed at the Baseline and Week 24 visits.Measure Description: The QoL-AD (Quality of Life - Alzheimer's Disease) is a commonly used 13 item QoL scale that assesses items specific to QoL in patients with cognitive impairment. It is administered to the research partner with answers for the patient. Points are assigned to each item as follows: poor = 1, fair = 2, good = 3, excellent = 4.The total score is the sum of all 13 items. The range of score is from 0-52. We calculated the change by subtracting the scores on week 24 score from baseline. A negative value indicates worsening quality of life.
Change in Digit SpanMean change in scores from baseline to week 24Measure Description: The Digit Span consists of repetition of increasing long strings of digits presented at 1 per second as read by the examiner and repeated by the subject.The score is the maximum number of digits the patient can repeat until they fail twice in a row. The reverse digit span is identical to the forward digit span except that the patient repeats the presented digits in reverse order. The score is the maximum number of digits the patient can repeat in reverse order until they fail twice in a row. Each correct response is worth one point with a maximum total score of 28. A higher score is better. We calculated change by subtracting week 24 score from baseline score. A negative score indicates worse performance over the course of study.

Countries

United States

Participant flow

Recruitment details

Patients were recruited based on physician referral from three Cleveland Clinic sites between May 2015 and January 2018

Pre-assignment details

Of 96 screened participants, 50 met inclusion criteria and were enrolled and randomized to treatment.

Participants by arm

ArmCount
Placebo
Subjects will be randomized in 1:1 ratio to receive Rasagiline or the matching placebo 24-week double blind treatment. Subjects will take one 0.5 mg Rasagiline tablet or the matching placebo once a day on Baseline (Day 1) through Week 4. The dose will be titrated up to one 1 mg tablet or the matching placebo once a day starting on Week 5 until the Week 28 (end of treatment visit). Placebo
25
Rasagiline
Subjects will be randomized in 1:1 ratio to receive Rasagiline or the matching placebo 24-week double blind treatment. Subjects will take one 0.5 mg Rasagiline tablet or the matching placebo once a day on Baseline (Day 1) through Week 4. The dose will be titrated up to one 1 mg tablet or the matching placebo once a day starting on Week 5 until the Week 28 (end of treatment visit). Rasagiline
25
Total50

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyLost to Follow-up34

Baseline characteristics

CharacteristicRasagilinePlaceboTotal
Age, Continuous74.72 years
STANDARD_DEVIATION 7.35
73.44 years
STANDARD_DEVIATION 7.12
74.08 years
STANDARD_DEVIATION 7.19
Alzheimer's Disease Assessment Scale - Cognitive 11 score23.2 units on a scale
STANDARD_DEVIATION 6
27.96 units on a scale
STANDARD_DEVIATION 10.53
25.58 units on a scale
STANDARD_DEVIATION 8.81
Alzheimer's Disease Cooperative Study - Activities of Daily Living (ADCS-ADL) score61.88 units on a scale
STANDARD_DEVIATION 8.44
58.2 units on a scale
STANDARD_DEVIATION 11.1
60 units on a scale
STANDARD_DEVIATION 9.96
Controlled Oral Word Association Test (cowat) score26.72 units on a scale
STANDARD_DEVIATION 12.6
21.16 units on a scale
STANDARD_DEVIATION 13.16
23.94 units on a scale
STANDARD_DEVIATION 13.06
digit span13.08 units on a scale
STANDARD_DEVIATION 2.75
11.76 units on a scale
STANDARD_DEVIATION 3.23
12.42 units on a scale
STANDARD_DEVIATION 3.04
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants0 Participants0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
25 Participants25 Participants50 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Mini Mental Status Examination (MMSE)21.24 units on a scale
STANDARD_DEVIATION 3.54
19.04 units on a scale
STANDARD_DEVIATION 4.61
20.14 units on a scale
STANDARD_DEVIATION 4.21
Neuropsychiatric Inventory (NPI) score7.62 units on a scale
STANDARD_DEVIATION 7.61
8.28 units on a scale
STANDARD_DEVIATION 8.97
7.96 units on a scale
STANDARD_DEVIATION 8.25
Quality of Life - Alzheimer's Disease (QoL-AD)36.73 units on a scale
STANDARD_DEVIATION 5.35
39.58 units on a scale
STANDARD_DEVIATION 5.24
38.22 units on a scale
STANDARD_DEVIATION 5.43
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
1 Participants0 Participants1 Participants
Race (NIH/OMB)
Black or African American
0 Participants1 Participants1 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
24 Participants24 Participants48 Participants
Region of Enrollment
United States
25 participants25 participants50 participants
Sex: Female, Male
Female
14 Participants11 Participants25 Participants
Sex: Female, Male
Male
11 Participants14 Participants25 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 250 / 25
other
Total, other adverse events
15 / 2516 / 25
serious
Total, serious adverse events
4 / 251 / 25

Outcome results

Primary

Change in Regional Glucose Metabolism Between Week 24 and Baseline as Measured by 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography (FDG-PET).

The primary outcome measure is the change from baseline to week 24 in FDG-PET as measured by Standard Uptake Units Regional (SUVR) in several pre-specified brain regions including the medial temporal, lateral temporal, posterior cingulate - precuneus, inferior parietal, middle frontal, anterior cingulate, and striatum. The SUVR change was calculated by subtracting the value at 24 weeks from baseline values. Negative values indicate increased hypometabolism (i.e. worsening of cell function).

Time frame: 24 weeks

ArmMeasureGroupValue (MEAN)Dispersion
PlaceboChange in Regional Glucose Metabolism Between Week 24 and Baseline as Measured by 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography (FDG-PET).Middle Frontal-0.032 SUVRStandard Deviation 0.03
PlaceboChange in Regional Glucose Metabolism Between Week 24 and Baseline as Measured by 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography (FDG-PET).Anterior Cingulate-0.020 SUVRStandard Deviation 0.021
PlaceboChange in Regional Glucose Metabolism Between Week 24 and Baseline as Measured by 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography (FDG-PET).Superior Frontal-0.016 SUVRStandard Deviation 0.022
PlaceboChange in Regional Glucose Metabolism Between Week 24 and Baseline as Measured by 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography (FDG-PET).Striatum-0.024 SUVRStandard Deviation 0.029
PlaceboChange in Regional Glucose Metabolism Between Week 24 and Baseline as Measured by 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography (FDG-PET).Medial Temporal-0.015 SUVRStandard Deviation 0.034
PlaceboChange in Regional Glucose Metabolism Between Week 24 and Baseline as Measured by 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography (FDG-PET).Lateral Temporal-0.020 SUVRStandard Deviation 0.029
PlaceboChange in Regional Glucose Metabolism Between Week 24 and Baseline as Measured by 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography (FDG-PET).Post Cingulate - Precuneus-0.017 SUVRStandard Deviation 0.023
PlaceboChange in Regional Glucose Metabolism Between Week 24 and Baseline as Measured by 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography (FDG-PET).Inferior Parietal-0.025 SUVRStandard Deviation 0.029
RasagilineChange in Regional Glucose Metabolism Between Week 24 and Baseline as Measured by 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography (FDG-PET).Inferior Parietal-0.018 SUVRStandard Deviation 0.022
RasagilineChange in Regional Glucose Metabolism Between Week 24 and Baseline as Measured by 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography (FDG-PET).Middle Frontal-0.011 SUVRStandard Deviation 0.03
RasagilineChange in Regional Glucose Metabolism Between Week 24 and Baseline as Measured by 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography (FDG-PET).Medial Temporal-0.010 SUVRStandard Deviation 0.034
RasagilineChange in Regional Glucose Metabolism Between Week 24 and Baseline as Measured by 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography (FDG-PET).Anterior Cingulate-0.003 SUVRStandard Deviation 0.026
RasagilineChange in Regional Glucose Metabolism Between Week 24 and Baseline as Measured by 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography (FDG-PET).Post Cingulate - Precuneus-0.016 SUVRStandard Deviation 0.018
RasagilineChange in Regional Glucose Metabolism Between Week 24 and Baseline as Measured by 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography (FDG-PET).Superior Frontal-0.003 SUVRStandard Deviation 0.018
RasagilineChange in Regional Glucose Metabolism Between Week 24 and Baseline as Measured by 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography (FDG-PET).Lateral Temporal-0.016 SUVRStandard Deviation 0.024
RasagilineChange in Regional Glucose Metabolism Between Week 24 and Baseline as Measured by 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography (FDG-PET).Striatum-0.002 SUVRStandard Deviation 0.028
Secondary

Change in ADAS-Cog 11 (Alzheimer's Disease Assessment Scale - Cognitive 11) Score

The ADAS-Cog 11 (Alzheimer's Disease Assessment Scale - Cognitive 11) is a psychometric instrument that evaluates memory, attention, reasoning, language, orientation, and praxis. A higher score indicates more impairment. Scores from the original portion of the test range from 0 (best) to 70 (worse). We used total ADAS-Cog 11 scores, which is a sum of individual subscales. We calculated the change by subtracting the ADAS Cog score at week 24 from baseline score. A positive change indicates cognitive worsening.

Time frame: Mean change in scores from baseline to week 24

ArmMeasureValue (MEAN)Dispersion
PlaceboChange in ADAS-Cog 11 (Alzheimer's Disease Assessment Scale - Cognitive 11) Score2.76 score on a scaleStandard Deviation 4.3
RasagilineChange in ADAS-Cog 11 (Alzheimer's Disease Assessment Scale - Cognitive 11) Score1.81 score on a scaleStandard Deviation 4.43
Secondary

Change in ADCS-ADL (Alzheimer's Disease Cooperative Study-Activities of Daily Living) Score

Measure Description: The ADCS-ADL (Alzheimer's Disease Cooperative Study-Activities of Daily Living) is an activities-of-daily-living inventory developed by the ADCS to assess functional performance in participants with AD. Using a structured interview format, study partners are queried as to whether participants attempted each item in the inventory during the past 4 weeks and their level of performance. The ADCS-ADL provides a total score from 0-78, with a lower score indicating greater severity. We calculated change by subtracting scores on week 24 test from the baseline score. A negative score indicates worsening ability to complete ADLs.

Time frame: Mean change in scores from baseline to week 24

ArmMeasureValue (MEAN)Dispersion
PlaceboChange in ADCS-ADL (Alzheimer's Disease Cooperative Study-Activities of Daily Living) Score-3.23 score on a scaleStandard Deviation 6.71
RasagilineChange in ADCS-ADL (Alzheimer's Disease Cooperative Study-Activities of Daily Living) Score-3.75 score on a scaleStandard Deviation 7.27
Secondary

Change in COWAT (Controlled Oral Word Association Test) Score

Measure Description: Study participants are instructed, I want to see how many words you can say beginning with a certain letter in one minute. The study participant's responses are recorded on the worksheet. Study participants are then given an additional one minute for each of two different letters using similar instructions. The score is the total number of acceptable words for the three trials combined. A higher score represents better performance. Responses are then judged for their acceptability (example for the use of proper nouns, numbers, repetitions and stem word with a different ending). The score is the total number of acceptable words for the three trials combined. A higher score represents better performance. We calculated change by subtracting week 24 scores from baseline scores. A negative score indicates worse performance.

Time frame: Mean change in scores from baseline to week 24

ArmMeasureValue (MEAN)Dispersion
PlaceboChange in COWAT (Controlled Oral Word Association Test) Score-1.09 score on a scaleStandard Deviation 6.31
RasagilineChange in COWAT (Controlled Oral Word Association Test) Score0.62 score on a scaleStandard Deviation 5.55
Secondary

Change in Digit Span

Measure Description: The Digit Span consists of repetition of increasing long strings of digits presented at 1 per second as read by the examiner and repeated by the subject.The score is the maximum number of digits the patient can repeat until they fail twice in a row. The reverse digit span is identical to the forward digit span except that the patient repeats the presented digits in reverse order. The score is the maximum number of digits the patient can repeat in reverse order until they fail twice in a row. Each correct response is worth one point with a maximum total score of 28. A higher score is better. We calculated change by subtracting week 24 score from baseline score. A negative score indicates worse performance over the course of study.

Time frame: Mean change in scores from baseline to week 24

ArmMeasureValue (MEAN)Dispersion
PlaceboChange in Digit Span-1.18 score on a scaleStandard Deviation 1.92
RasagilineChange in Digit Span-0.29 score on a scaleStandard Deviation 3.08
Secondary

Change in MMSE (Mini Mental Status Examination) Score

Measure Description: The MMSE (Mini Mental Status Examination) is a brief, frequently used screening instrument for AD drug studies. The MMSE evaluates orientation, memory, attention, concentration, naming, repetition, comprehension, and ability to create a sentence and to copy two overlapping pentagons. A lower score indicates more cognitive impairment. The highest score is 30, range is between 0 (severe impairment) and 30 (cognitively normal). We calculated the change in scores by subtracting week 24 score from baseline. A negative score indicates clinical worsening.

Time frame: Mean change in scores from baseline to week 24

ArmMeasureValue (MEAN)Dispersion
PlaceboChange in MMSE (Mini Mental Status Examination) Score-1.14 score on a scaleStandard Deviation 2.27
RasagilineChange in MMSE (Mini Mental Status Examination) Score-0.65 score on a scaleStandard Deviation 2.48
Secondary

Change in NPI (Neuropsychiatric Inventory) Score

Measure Description: The behavioral outcome measure for this trial is the NPI (Neuropsychiatric Inventory). The NPI evaluates both the frequency and severity of 10 neuropsychiatric disturbances. Frequency assessments range from 1 (occasionally, less than once per week) to 4 (very frequently, once or more per day or continuously) as well as severity (1=mild, 2=moderate, 3=severe). The overall score is calculated by summing the severity and frequency of the subscale measures. The range of scores is 0-40. A score of 0 indicates no behavioral impairment and a score of 40 indicates severe behavioral impairment. We calculated change by subtracting Week 24 scores from baseline scores. A positive change indicates behavioral worsening.

Time frame: Mean change in scores from baseline to week 24

ArmMeasureValue (MEAN)Dispersion
PlaceboChange in NPI (Neuropsychiatric Inventory) Score2 score on a scaleStandard Deviation 7.18
RasagilineChange in NPI (Neuropsychiatric Inventory) Score0.2 score on a scaleStandard Deviation 6.79
Secondary

Change in QoL-AD (Quality of Life - Alzheimer's Disease) Score

Measure Description: The QoL-AD (Quality of Life - Alzheimer's Disease) is a commonly used 13 item QoL scale that assesses items specific to QoL in patients with cognitive impairment. It is administered to the research partner with answers for the patient. Points are assigned to each item as follows: poor = 1, fair = 2, good = 3, excellent = 4.The total score is the sum of all 13 items. The range of score is from 0-52. We calculated the change by subtracting the scores on week 24 score from baseline. A negative value indicates worsening quality of life.

Time frame: This assessment will be performed at the Baseline and Week 24 visits.

ArmMeasureValue (MEAN)Dispersion
PlaceboChange in QoL-AD (Quality of Life - Alzheimer's Disease) Score-1.95 score on a scaleStandard Deviation 3.28
RasagilineChange in QoL-AD (Quality of Life - Alzheimer's Disease) Score1.11 score on a scaleStandard Deviation 3.77

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026