Trial Outcomes & Findings for K0706 for Patients Diagnosed With Dementia With Lewy Bodies (NCT NCT03996460)
NCT ID: NCT03996460
Last Updated: 2026-06-08
Results Overview
The investigators will determine safety and tolerability by using the occurrence of adverse events (AEs) of interest, including myelosuppression, urinary, pancreatic and hepatic disorders, gastrointestinal (GI), kidney disorders, Corrected QT-interval (QTc)prolongation as per SPARC Ltd Investigator Brochure (IB).
TERMINATED
PHASE2
29 participants
12 weeks
2026-06-08
Participant Flow
Participant milestones
| Measure |
Placebo Powder
Placebo: Ten (10) patients in group 1 received the sachet of matching placebo (equivalent to a capsule of placebo "sugar pill") orally daily for 12 weeks (90 days) without food.
|
192 mg Powder of K0706
192 mg powder of K0706: Ten (10) patients in group 2 received the sachet of 192 mg powder of K0706 (equivalent to 96 mg capsule of K0706) orally for 12 weeks (90 days) without food.
|
384 mg Powder of K0706
384 mg powder of K0706: Nine (9) patients in group 3 received the 384 mg powder of K0706 (equivalent to 192 capsule of K0706) orally daily for 12 weeks (90 days) without food.
|
|---|---|---|---|
|
Overall Study
STARTED
|
10
|
10
|
9
|
|
Overall Study
COMPLETED
|
8
|
10
|
4
|
|
Overall Study
NOT COMPLETED
|
2
|
0
|
5
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
K0706 for Patients Diagnosed With Dementia With Lewy Bodies
Baseline characteristics by cohort
| Measure |
Placebo Powder
n=10 Participants
Placebo: Ten (10) patients in group 1 received the sachet of matching placebo (equivalent to a capsule of placebo "sugar pill") orally daily for 12 weeks (90 days) without food.
|
192 mg Powder of K0706
n=10 Participants
192 mg powder of K0706: Ten (10) patients in group 2 received the sachet of 192 mg powder of K0706 (equivalent to 96 mg capsule of K0706) orally for 12 weeks (90 days) without food.
|
384 mg Powder of K0706
n=9 Participants
384 mg powder of K0706: Nine (9) patients in group 3 received the 384 mg powder of K0706 (equivalent to 192 capsule of K0706) orally daily for 12 weeks (90 days) without food.
|
Total
n=29 Participants
Total of all reporting groups
|
|---|---|---|---|---|
|
Age, Categorical
<=18 years
|
0 Participants
n=9 Participants
|
0 Participants
n=27 Participants
|
0 Participants
n=267 Participants
|
0 Participants
n=265 Participants
|
|
Age, Categorical
Between 18 and 65 years
|
0 Participants
n=9 Participants
|
0 Participants
n=27 Participants
|
0 Participants
n=267 Participants
|
0 Participants
n=265 Participants
|
|
Age, Categorical
>=65 years
|
10 Participants
n=9 Participants
|
10 Participants
n=27 Participants
|
9 Participants
n=267 Participants
|
29 Participants
n=265 Participants
|
|
Age, Continuous
|
73 years
STANDARD_DEVIATION 6 • n=9 Participants
|
76 years
STANDARD_DEVIATION 6 • n=27 Participants
|
80 years
STANDARD_DEVIATION 6 • n=267 Participants
|
77 years
STANDARD_DEVIATION 6 • n=265 Participants
|
|
Sex: Female, Male
Female
|
9 Participants
n=9 Participants
|
9 Participants
n=27 Participants
|
7 Participants
n=267 Participants
|
25 Participants
n=265 Participants
|
|
Sex: Female, Male
Male
|
1 Participants
n=9 Participants
|
1 Participants
n=27 Participants
|
2 Participants
n=267 Participants
|
4 Participants
n=265 Participants
|
|
Race (NIH/OMB)
American Indian or Alaska Native
|
0 Participants
n=9 Participants
|
0 Participants
n=27 Participants
|
0 Participants
n=267 Participants
|
0 Participants
n=265 Participants
|
|
Race (NIH/OMB)
Asian
|
1 Participants
n=9 Participants
|
0 Participants
n=27 Participants
|
1 Participants
n=267 Participants
|
2 Participants
n=265 Participants
|
|
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
|
0 Participants
n=9 Participants
|
0 Participants
n=27 Participants
|
0 Participants
n=267 Participants
|
0 Participants
n=265 Participants
|
|
Race (NIH/OMB)
Black or African American
|
0 Participants
n=9 Participants
|
1 Participants
n=27 Participants
|
0 Participants
n=267 Participants
|
1 Participants
n=265 Participants
|
|
Race (NIH/OMB)
White
|
9 Participants
n=9 Participants
|
8 Participants
n=27 Participants
|
8 Participants
n=267 Participants
|
25 Participants
n=265 Participants
|
|
Race (NIH/OMB)
More than one race
|
0 Participants
n=9 Participants
|
0 Participants
n=27 Participants
|
0 Participants
n=267 Participants
|
0 Participants
n=265 Participants
|
|
Race (NIH/OMB)
Unknown or Not Reported
|
0 Participants
n=9 Participants
|
1 Participants
n=27 Participants
|
0 Participants
n=267 Participants
|
1 Participants
n=265 Participants
|
|
Region of Enrollment
United States
|
10 participants
n=9 Participants
|
10 participants
n=27 Participants
|
9 participants
n=267 Participants
|
29 participants
n=265 Participants
|
PRIMARY outcome
Timeframe: 12 weeksThe investigators will determine safety and tolerability by using the occurrence of adverse events (AEs) of interest, including myelosuppression, urinary, pancreatic and hepatic disorders, gastrointestinal (GI), kidney disorders, Corrected QT-interval (QTc)prolongation as per SPARC Ltd Investigator Brochure (IB).
Outcome measures
| Measure |
Placebo Powder
n=8 Participants
Placebo: Ten (10) patients in group 1 received the sachet of matching placebo (equivalent to a capsule of placebo "sugar pill") orally daily for 12 weeks (90 days) without food.
|
192 mg Powder of K0706
n=10 Participants
192 mg powder of K0706: Ten (10) patients in group 2 received the sachet of 192 mg powder of K0706 (equivalent to 96 mg capsule of K0706) orally for 12 weeks (90 days) without food.
|
384 mg Powder of K0706
n=4 Participants
384 mg powder of K0706: Nine (9) patients in group 3 received the 384 mg powder of K0706 (equivalent to 192 capsule of K0706) orally daily for 12 weeks (90 days) without food.
|
|---|---|---|---|
|
Evidence of Treatment-emergent Adverse Effects (Safety and Tolerability)
|
56 events
|
19 events
|
6 events
|
SECONDARY outcome
Timeframe: Baseline, End of Treatment (EOT), and the change between baseline and EOTPopulation: The mean difference within groups at baseline and end of treatment.
DLB related plasma biomarkers, including alpha-synuclein, HVA, DOPAC were measured at Baseline and 12 weeks.
Outcome measures
| Measure |
Placebo Powder
n=7 Participants
Placebo: Ten (10) patients in group 1 received the sachet of matching placebo (equivalent to a capsule of placebo "sugar pill") orally daily for 12 weeks (90 days) without food.
|
192 mg Powder of K0706
n=8 Participants
192 mg powder of K0706: Ten (10) patients in group 2 received the sachet of 192 mg powder of K0706 (equivalent to 96 mg capsule of K0706) orally for 12 weeks (90 days) without food.
|
384 mg Powder of K0706
n=4 Participants
384 mg powder of K0706: Nine (9) patients in group 3 received the 384 mg powder of K0706 (equivalent to 192 capsule of K0706) orally daily for 12 weeks (90 days) without food.
|
|---|---|---|---|
|
Measurement of Plasma Biomarkers in DLB Patients
alpha-synuclein (EOT)
|
7161.74 pg/ml
Standard Deviation 4145.22
|
7699.78 pg/ml
Standard Deviation 3927.16
|
6907.39 pg/ml
Standard Deviation 2376.65
|
|
Measurement of Plasma Biomarkers in DLB Patients
Homovanillic-acid (HVA) (Baseline)
|
13.46 pg/ml
Standard Deviation 0.25
|
13.39 pg/ml
Standard Deviation 0.23
|
13.47 pg/ml
Standard Deviation 0.16
|
|
Measurement of Plasma Biomarkers in DLB Patients
Homovanillic-acid (HVA) (EOT)
|
13.22 pg/ml
Standard Deviation 0.29
|
13.00 pg/ml
Standard Deviation 0.39
|
12.98 pg/ml
Standard Deviation 0.33
|
|
Measurement of Plasma Biomarkers in DLB Patients
Dopamine (Baseline)
|
6.03 pg/ml
Standard Deviation 0.04
|
6.04 pg/ml
Standard Deviation 0.05
|
6.00 pg/ml
Standard Deviation 0.05
|
|
Measurement of Plasma Biomarkers in DLB Patients
Dopamine (EOT)
|
6.00 pg/ml
Standard Deviation 0.02
|
6.03 pg/ml
Standard Deviation 0.05
|
5.99 pg/ml
Standard Deviation 0.05
|
|
Measurement of Plasma Biomarkers in DLB Patients
alpha-synuclein (Baseline)
|
9264.84 pg/ml
Standard Deviation 4284.17
|
7776.96 pg/ml
Standard Deviation 2309.02
|
14907.39 pg/ml
Standard Deviation 5543.71
|
|
Measurement of Plasma Biomarkers in DLB Patients
Dopamine
|
-0.03 pg/ml
Standard Deviation 0.05
|
-0.01 pg/ml
Standard Deviation 0.02
|
-0.01 pg/ml
Standard Deviation 0.03
|
|
Measurement of Plasma Biomarkers in DLB Patients
alpha-synuclein
|
-2103.11 pg/ml
Standard Deviation 6444.20
|
-77.17 pg/ml
Standard Deviation 5298.33
|
-8000.00 pg/ml
Standard Deviation 6083.35
|
|
Measurement of Plasma Biomarkers in DLB Patients
Homovanillic-acid (HVA)
|
-0.25 pg/ml
Standard Deviation 0.30
|
-0.39 pg/ml
Standard Deviation 0.43
|
-0.49 pg/ml
Standard Deviation 0.39
|
SECONDARY outcome
Timeframe: Baseline, End of Treatment (EOT) (12 weeks), and the change between baseline and EOTPopulation: The mean difference within groups at baseline and end of treatment.
Concentration of DLB related CSF biomarkers, including HVA, DOPAC, Abeta40/42, total tau, ptau231/181 and total and oligomeric alpha-synuclein were measured at Baseline and 12 weeks.
Outcome measures
| Measure |
Placebo Powder
n=7 Participants
Placebo: Ten (10) patients in group 1 received the sachet of matching placebo (equivalent to a capsule of placebo "sugar pill") orally daily for 12 weeks (90 days) without food.
|
192 mg Powder of K0706
n=8 Participants
192 mg powder of K0706: Ten (10) patients in group 2 received the sachet of 192 mg powder of K0706 (equivalent to 96 mg capsule of K0706) orally for 12 weeks (90 days) without food.
|
384 mg Powder of K0706
n=4 Participants
384 mg powder of K0706: Nine (9) patients in group 3 received the 384 mg powder of K0706 (equivalent to 192 capsule of K0706) orally daily for 12 weeks (90 days) without food.
|
|---|---|---|---|
|
Measurement of Biomarker Concentration in CSF
beta-amyloid(42) (AB42)
|
3.98 pg/ml
Standard Deviation 82.27
|
-9.27 pg/ml
Standard Deviation 55.54
|
-44.73 pg/ml
Standard Deviation 105.14
|
|
Measurement of Biomarker Concentration in CSF
Total (t) Tau
|
-9.53 pg/ml
Standard Deviation 20.03
|
-13.58 pg/ml
Standard Deviation 25.73
|
-1.83 pg/ml
Standard Deviation 44.77
|
|
Measurement of Biomarker Concentration in CSF
Phospho(p)-Tau(181)
|
-6.53 pg/ml
Standard Deviation 20.98
|
-12.55 pg/ml
Standard Deviation 18.99
|
-8.03 pg/ml
Standard Deviation 32.57
|
|
Measurement of Biomarker Concentration in CSF
alpha-synuclein (Baseline)
|
1105.83 pg/ml
Standard Deviation 698.59
|
2349.49 pg/ml
Standard Deviation 2433.62
|
1245.92 pg/ml
Standard Deviation 400.63
|
|
Measurement of Biomarker Concentration in CSF
alpha-synuclein (EOT)
|
1053.94 pg/ml
Standard Deviation 279.94
|
1115.31 pg/ml
Standard Deviation 367.17
|
1272.96 pg/ml
Standard Deviation 727.13
|
|
Measurement of Biomarker Concentration in CSF
beta-amyloid(40) (AB40) (Baseline)
|
1776.29 pg/ml
Standard Deviation 397.93
|
1715.75 pg/ml
Standard Deviation 386.01
|
2271.50 pg/ml
Standard Deviation 890.37
|
|
Measurement of Biomarker Concentration in CSF
alpha-synuclein
|
-51.90 pg/ml
Standard Deviation 640.60
|
-1234.18 pg/ml
Standard Deviation 2344.69
|
27.04 pg/ml
Standard Deviation 365.25
|
|
Measurement of Biomarker Concentration in CSF
beta-amyloid(40) (AB40)
|
85.86 pg/ml
Standard Deviation 386.12
|
140.75 pg/ml
Standard Deviation 372.09
|
-46.25 pg/ml
Standard Deviation 384.96
|
|
Measurement of Biomarker Concentration in CSF
beta-amyloid(40) (AB40) (EOT)
|
1862.14 pg/ml
Standard Deviation 632.15
|
1856.50 pg/ml
Standard Deviation 564.18
|
2225.25 pg/ml
Standard Deviation 803.96
|
|
Measurement of Biomarker Concentration in CSF
beta-amyloid(42) (AB42) (Baseline)
|
317.66 pg/ml
Standard Deviation 95.93
|
284.29 pg/ml
Standard Deviation 52.86
|
388.20 pg/ml
Standard Deviation 143.68
|
|
Measurement of Biomarker Concentration in CSF
beta-amyloid(42) (AB42) (EOT)
|
321.64 pg/ml
Standard Deviation 127.08
|
275.02 pg/ml
Standard Deviation 78.42
|
343.48 pg/ml
Standard Deviation 139.22
|
|
Measurement of Biomarker Concentration in CSF
Total (t) Tau (Baseline)
|
148.65 pg/ml
Standard Deviation 48.87
|
169.13 pg/ml
Standard Deviation 59.31
|
180.93 pg/ml
Standard Deviation 54.67
|
|
Measurement of Biomarker Concentration in CSF
Total (t) Tau (EOT)
|
139.12 pg/ml
Standard Deviation 56.50
|
155.55 pg/ml
Standard Deviation 66.76
|
179.10 pg/ml
Standard Deviation 84.47
|
|
Measurement of Biomarker Concentration in CSF
Phospho(p)-Tau(181) (Baseline)
|
82.82 pg/ml
Standard Deviation 46.62
|
106.43 pg/ml
Standard Deviation 66.67
|
101.78 pg/ml
Standard Deviation 23.51
|
|
Measurement of Biomarker Concentration in CSF
Phospho(p)-Tau(181) (EOT)
|
76.29 pg/ml
Standard Deviation 35.26
|
93.88 pg/ml
Standard Deviation 59.71
|
93.75 pg/ml
Standard Deviation 46.29
|
SECONDARY outcome
Timeframe: Baseline, End of Treatment (EOT), and the change between baseline and EOTPopulation: The mean difference within groups at baseline and end of treatment.
Ratio of HVA to Dopamine, and Dopamine to HVA in the plasma at Baseline, and 12 weeks The ratio of HVA to DA is a biochemical marker used to measure dopamine turnover, reflecting the rate at which dopamine is synthesized, released, and subsequently broken down in the central nervous system. High Ratio: Indicates rapid metabolism/degradation of dopamine. Low Ratio: May suggest lower turnover or reduced activity in dopaminergic pathways. HVA/DOPAC Ratio (Optimal): 0.1 - 1.8.; a ratio above 1.8 suggests accelerated turnover, typically seen in Parkinson's Disease
Outcome measures
| Measure |
Placebo Powder
n=7 Participants
Placebo: Ten (10) patients in group 1 received the sachet of matching placebo (equivalent to a capsule of placebo "sugar pill") orally daily for 12 weeks (90 days) without food.
|
192 mg Powder of K0706
n=8 Participants
192 mg powder of K0706: Ten (10) patients in group 2 received the sachet of 192 mg powder of K0706 (equivalent to 96 mg capsule of K0706) orally for 12 weeks (90 days) without food.
|
384 mg Powder of K0706
n=4 Participants
384 mg powder of K0706: Nine (9) patients in group 3 received the 384 mg powder of K0706 (equivalent to 192 capsule of K0706) orally daily for 12 weeks (90 days) without food.
|
|---|---|---|---|
|
Measurement of Plasma Biomarkers in DLB Patients
HVA/Dopamine
|
-0.03 ratio
Standard Deviation 0.06
|
-0.06 ratio
Standard Deviation 0.07
|
-0.08 ratio
Standard Deviation 0.07
|
|
Measurement of Plasma Biomarkers in DLB Patients
HVA/Dopamine (Baseline)
|
2.23 ratio
Standard Deviation 0.04
|
2.22 ratio
Standard Deviation 0.04
|
2.25 ratio
Standard Deviation 0.03
|
|
Measurement of Plasma Biomarkers in DLB Patients
HVA/Dopamine (EOT)
|
2.20 ratio
Standard Deviation 0.05
|
2.16 ratio
Standard Deviation 0.07
|
2.17 ratio
Standard Deviation 0.06
|
SECONDARY outcome
Timeframe: Baseline, End of Treatment (EOT) (12 weeks), and the change between baseline and EOTPopulation: The mean difference within groups at baseline and end of treatment.
Ratio of DLB related CSF biomarkers, including Abeta42 to Abeta40, phospho-Tau(181) to Abeta42, and phospho-tau181 to Total Tau at Baseline and 12 weeks. Ab42/Ab40 ratio is a biomarker used to assess Alzheimer's disease (AD) risk. A lower ratio indicates a higher likelihood of amyloid plaque accumulation in the brain and AD pathology. The ptau(181)/Ab42 ratio is a clinical biomarker used to identify AD pathology by measuring the balance between tau protein phosphorylation and amyloid-beta accumulation. Higher ratio values typically indicate a higher likelihood of amyloid and tau pathology in the brain. P-tau181 and its ratio to total tau (t-tau) or other amyloid markers are effective indicators of AD pathology. Reference Range/Ratio: A 95% reference interval for the p-tau181/t-tau ratio has been reported as 0.38-6.34, with higher values indicating a higher likelihood of AD pathology.
Outcome measures
| Measure |
Placebo Powder
n=7 Participants
Placebo: Ten (10) patients in group 1 received the sachet of matching placebo (equivalent to a capsule of placebo "sugar pill") orally daily for 12 weeks (90 days) without food.
|
192 mg Powder of K0706
n=8 Participants
192 mg powder of K0706: Ten (10) patients in group 2 received the sachet of 192 mg powder of K0706 (equivalent to 96 mg capsule of K0706) orally for 12 weeks (90 days) without food.
|
384 mg Powder of K0706
n=4 Participants
384 mg powder of K0706: Nine (9) patients in group 3 received the 384 mg powder of K0706 (equivalent to 192 capsule of K0706) orally daily for 12 weeks (90 days) without food.
|
|---|---|---|---|
|
Measurement of CSF Biomarkers in DLB Patients
AB42/AB40
|
-0.14 ratio
Standard Deviation 0.08
|
-0.01 ratio
Standard Deviation 0.03
|
-0.03 ratio
Standard Deviation 0.04
|
|
Measurement of CSF Biomarkers in DLB Patients
p-Tau(181)/AB42
|
-0.03 ratio
Standard Deviation 0.10
|
-0.04 ratio
Standard Deviation 0.06
|
-0.10 ratio
Standard Deviation 0.11
|
|
Measurement of CSF Biomarkers in DLB Patients
pTau(181)/tTau
|
0.03 ratio
Standard Deviation 0.23
|
-0.02 ratio
Standard Deviation 0.19
|
-0.15 ratio
Standard Deviation 0.24
|
|
Measurement of CSF Biomarkers in DLB Patients
AB42/AB40 (Baseline)
|
0.32 ratio
Standard Deviation 0.13
|
0.17 ratio
Standard Deviation 0.04
|
0.17 ratio
Standard Deviation 0.04
|
|
Measurement of CSF Biomarkers in DLB Patients
AB42/AB40 (EOT)
|
0.18 ratio
Standard Deviation 0.07
|
0.16 ratio
Standard Deviation 0.15
|
0.14 ratio
Standard Deviation 0.06
|
|
Measurement of CSF Biomarkers in DLB Patients
p-Tau(181)/AB42 (Baseline)
|
0.32 ratio
Standard Deviation 0.26
|
0.41 ratio
Standard Deviation 0.28
|
0.28 ratio
Standard Deviation 0.05
|
|
Measurement of CSF Biomarkers in DLB Patients
p-Tau(181)/AB42 (EOT)
|
0.29 ratio
Standard Deviation 0.18
|
0.37 ratio
Standard Deviation 0.23
|
0.18 ratio
Standard Deviation 0.09
|
|
Measurement of CSF Biomarkers in DLB Patients
pTau(181)/tTau (Baseline)
|
0.53 ratio
Standard Deviation 0.21
|
0.60 ratio
Standard Deviation 0.28
|
0.57 ratio
Standard Deviation 0.05
|
|
Measurement of CSF Biomarkers in DLB Patients
pTau(181)/tTau (EOT)
|
0.56 ratio
Standard Deviation 0.14
|
0.58 ratio
Standard Deviation 0.19
|
0.42 ratio
Standard Deviation 0.21
|
OTHER_PRE_SPECIFIED outcome
Timeframe: Baseline, 12 weeks (EOT), and change between Baseline and End of Treatment (EOT)Population: Median and Interquartile Range (IQR) are robust, non-parametric statistics used to describe central tendency and dispersion when outliers are present. The median represents the 50th percentile, while the IQR measures the spread of the middle 50% of the data. The number shown is the median value, not the mean value.
The MoCA is designed as a rapid screening instrument for mild cognitive dysfunction. It assesses different cognitive domains, including attention and concentration, executive functions, memory, language, visuo-constructional skills, conceptual thinking, calculations and orientation. Scores range between 0 and 30 where 30 is the highest score and 0 is the lowest score.
Outcome measures
| Measure |
Placebo Powder
n=7 Participants
Placebo: Ten (10) patients in group 1 received the sachet of matching placebo (equivalent to a capsule of placebo "sugar pill") orally daily for 12 weeks (90 days) without food.
|
192 mg Powder of K0706
n=10 Participants
192 mg powder of K0706: Ten (10) patients in group 2 received the sachet of 192 mg powder of K0706 (equivalent to 96 mg capsule of K0706) orally for 12 weeks (90 days) without food.
|
384 mg Powder of K0706
n=4 Participants
384 mg powder of K0706: Nine (9) patients in group 3 received the 384 mg powder of K0706 (equivalent to 192 capsule of K0706) orally daily for 12 weeks (90 days) without food.
|
|---|---|---|---|
|
Measurement of the Effects of K0706 on Cognition Using the Montreal Cognitive Assessment (MoCA) at Baseline and 12 Weeks
MOCA (Baseline)
|
24 score on a scale
Interval 21.5 to 25.5
|
23.5 score on a scale
Interval 20.5 to 27.75
|
26 score on a scale
Interval 24.0 to 27.0
|
|
Measurement of the Effects of K0706 on Cognition Using the Montreal Cognitive Assessment (MoCA) at Baseline and 12 Weeks
MOCA
|
-1 score on a scale
Interval -1.5 to 0.5
|
-1 score on a scale
Interval -2.0 to 0.75
|
0 score on a scale
Interval -1.5 to 0.25
|
|
Measurement of the Effects of K0706 on Cognition Using the Montreal Cognitive Assessment (MoCA) at Baseline and 12 Weeks
MOCA(EOT)
|
24 score on a scale
Interval 20.0 to 25.5
|
23 score on a scale
Interval 19.25 to 27.5
|
27 score on a scale
Interval 22.25 to 28.5
|
OTHER_PRE_SPECIFIED outcome
Timeframe: 12 weeksPopulation: Median and Interquartile Range (IQR) are robust, non-parametric statistics used to describe central tendency and dispersion when outliers are present. The median represents the 50th percentile, while the IQR measures the spread of the middle 50% of the data. The number shown is the median value, not the mean value.
The Trail Making Test (TMT) is a neuropsychological test of visual attention and task switching. It consists of two parts in which the subject is instructed to connect a set of 25 dots as quickly as possible while still maintaining accuracy. The test can provide information about visual search speed, scanning, speed of processing, mental flexibility, as well as executive functioning. The time to complete the test is measured in seconds. Lower times indicate better executive function, while higher scores suggest impairment.
Outcome measures
| Measure |
Placebo Powder
n=7 Participants
Placebo: Ten (10) patients in group 1 received the sachet of matching placebo (equivalent to a capsule of placebo "sugar pill") orally daily for 12 weeks (90 days) without food.
|
192 mg Powder of K0706
n=10 Participants
192 mg powder of K0706: Ten (10) patients in group 2 received the sachet of 192 mg powder of K0706 (equivalent to 96 mg capsule of K0706) orally for 12 weeks (90 days) without food.
|
384 mg Powder of K0706
n=4 Participants
384 mg powder of K0706: Nine (9) patients in group 3 received the 384 mg powder of K0706 (equivalent to 192 capsule of K0706) orally daily for 12 weeks (90 days) without food.
|
|---|---|---|---|
|
Measurement of the Effects of K0706 on Cognition Using the Trail Making Test (TMT)
TMT
|
-60 seconds
Interval -93.0 to -4.0
|
0 seconds
Interval -36.0 to 4.0
|
15.50 seconds
Interval 8.25 to 20.0
|
|
Measurement of the Effects of K0706 on Cognition Using the Trail Making Test (TMT)
TMT (Baseline)
|
300 seconds
Interval 275.0 to 330.0
|
300 seconds
Interval 163.0 to 300.0
|
80 seconds
Interval 80.0 to 212.0
|
|
Measurement of the Effects of K0706 on Cognition Using the Trail Making Test (TMT)
TMT (EOT)
|
290 seconds
Interval 212.0 to 300.0
|
220.5 seconds
Interval 141.75 to 300.0
|
161.5 seconds
Interval 98.5 to 242.25
|
OTHER_PRE_SPECIFIED outcome
Timeframe: 12 weeksPopulation: Median and Interquartile Range (IQR) are robust, non-parametric statistics used to describe central tendency and dispersion when outliers are present. The median represents the 50th percentile, while the IQR measures the spread of the middle 50% of the data. The number shown is the median value, not the mean value.
The 14-item Alzheimer's Disease Assessment Scale-Cognitive subscale (ADAS-Cog14) measures cognitive impairment, with higher scores (0-90) indicating greater disability.
Outcome measures
| Measure |
Placebo Powder
n=7 Participants
Placebo: Ten (10) patients in group 1 received the sachet of matching placebo (equivalent to a capsule of placebo "sugar pill") orally daily for 12 weeks (90 days) without food.
|
192 mg Powder of K0706
n=10 Participants
192 mg powder of K0706: Ten (10) patients in group 2 received the sachet of 192 mg powder of K0706 (equivalent to 96 mg capsule of K0706) orally for 12 weeks (90 days) without food.
|
384 mg Powder of K0706
n=4 Participants
384 mg powder of K0706: Nine (9) patients in group 3 received the 384 mg powder of K0706 (equivalent to 192 capsule of K0706) orally daily for 12 weeks (90 days) without food.
|
|---|---|---|---|
|
Measure the Effects of NIlotinib on Cognition Using the Alzheimer's Disease Assessment Scale - Cognitive (ADAS-cog14).
ADAS-cog
|
-1 score on a scale
Interval -2.17 to 5.67
|
-1.34 score on a scale
Interval -4.58 to 1.67
|
-0.50 score on a scale
Interval -2.25 to 0.92
|
|
Measure the Effects of NIlotinib on Cognition Using the Alzheimer's Disease Assessment Scale - Cognitive (ADAS-cog14).
ADAS-cog (Baseline)
|
22.33 score on a scale
Interval 19.67 to 31.0
|
24 score on a scale
Interval 17.16 to 41.17
|
24.33 score on a scale
Interval 24.0 to 30.0
|
|
Measure the Effects of NIlotinib on Cognition Using the Alzheimer's Disease Assessment Scale - Cognitive (ADAS-cog14).
ADAS-cog (EOT)
|
20.33 score on a scale
Interval 19.66 to 30.34
|
20.66 score on a scale
Interval 17.33 to 35.67
|
21 score on a scale
Interval 15.5 to 30.25
|
OTHER_PRE_SPECIFIED outcome
Timeframe: 12 weeksPopulation: Median and Interquartile Range (IQR) are robust, non-parametric statistics used to describe central tendency and dispersion when outliers are present. The median represents the 50th percentile, while the IQR measures the spread of the middle 50% of the data. The number shown is the median value, not the mean value.
ADCS-ADL is an activity of daily living inventory to assess functional performance. Using a structured interview format, study partners are queried as to whether participants attempted each item in the inventory during the prior 4 weeks and their level of performance. The ADCS-ADL includes some items from traditional basic ADL tests as well as instrumental (complex) activities of daily living. It is a 23 item scale that provide a total score from 0-78 with a lower score indicating greater severity; 0 is the minimum score and 78 is the maximum score.
Outcome measures
| Measure |
Placebo Powder
n=7 Participants
Placebo: Ten (10) patients in group 1 received the sachet of matching placebo (equivalent to a capsule of placebo "sugar pill") orally daily for 12 weeks (90 days) without food.
|
192 mg Powder of K0706
n=10 Participants
192 mg powder of K0706: Ten (10) patients in group 2 received the sachet of 192 mg powder of K0706 (equivalent to 96 mg capsule of K0706) orally for 12 weeks (90 days) without food.
|
384 mg Powder of K0706
n=4 Participants
384 mg powder of K0706: Nine (9) patients in group 3 received the 384 mg powder of K0706 (equivalent to 192 capsule of K0706) orally daily for 12 weeks (90 days) without food.
|
|---|---|---|---|
|
Measuring the Effects of K0706 on Behavior Using the Alzheimer's Disease Cooperative Study-Activity of Daily Living Scale.
ADCS-ADL
|
0 score on a scale
Interval -1.5 to 2.0
|
0 score on a scale
Interval -6.25 to 3.0
|
-1.50 score on a scale
Interval -5.0 to 0.25
|
|
Measuring the Effects of K0706 on Behavior Using the Alzheimer's Disease Cooperative Study-Activity of Daily Living Scale.
ADCS-ADL (Baseline)
|
66 score on a scale
Interval 63.5 to 71.0
|
66 score on a scale
Interval 57.0 to 70.75
|
66 score on a scale
Interval 61.0 to 72.0
|
|
Measuring the Effects of K0706 on Behavior Using the Alzheimer's Disease Cooperative Study-Activity of Daily Living Scale.
ADCS-ADL (EOT)
|
71 score on a scale
Interval 62.0 to 72.5
|
67 score on a scale
Interval 57.75 to 72.25
|
69.5 score on a scale
Interval 62.0 to 73.5
|
OTHER_PRE_SPECIFIED outcome
Timeframe: 12 weeksPopulation: Median and Interquartile Range (IQR) are robust, non-parametric statistics used to describe central tendency and dispersion when outliers are present. The median represents the 50th percentile, while the IQR measures the spread of the middle 50% of the data. The number shown is the median value, not the mean value.
UPDRS-I-III is used to follow the longitudinal course of Parkinson's disease. The UPDRS is made up of these sections: Part I: evaluation of mentation, behavior, and mood. Part II: self-evaluation of the activities of daily life (ADLs) Part III: clinician-scored monitored motor evaluation. Part IV: complications of therapy. Part V: Hoehn and Yahr staging of severity of Parkinson's disease. The minimum possible score on the UPDRS is 0, which indicates no disability or no symptoms of Parkinson's disease. The scale, used to assess severity, typically ranges from 0 to 199 (total) (199 being the maximum) or 0 to 108 (motor section, Part III) (108 being maximum). Higher scores on the Unified Parkinson's Disease Rating Scale (UPDRS) Parts I-III indicate increased severity of disease, greater disability, and more significant impairment, while lower scores signify better function.
Outcome measures
| Measure |
Placebo Powder
n=7 Participants
Placebo: Ten (10) patients in group 1 received the sachet of matching placebo (equivalent to a capsule of placebo "sugar pill") orally daily for 12 weeks (90 days) without food.
|
192 mg Powder of K0706
n=10 Participants
192 mg powder of K0706: Ten (10) patients in group 2 received the sachet of 192 mg powder of K0706 (equivalent to 96 mg capsule of K0706) orally for 12 weeks (90 days) without food.
|
384 mg Powder of K0706
n=4 Participants
384 mg powder of K0706: Nine (9) patients in group 3 received the 384 mg powder of K0706 (equivalent to 192 capsule of K0706) orally daily for 12 weeks (90 days) without food.
|
|---|---|---|---|
|
Measuring the Effects of K0706 on Motor Function by Using the Unified Parkinson's Disease Rating Scale (UPDRS)-I-III.
UPDRS-I-III
|
5 score on a scale
Interval -1.0 to 9.5
|
1 score on a scale
Interval -1.5 to 3.0
|
5 score on a scale
Interval -1.5 to 11.25
|
|
Measuring the Effects of K0706 on Motor Function by Using the Unified Parkinson's Disease Rating Scale (UPDRS)-I-III.
UPDRS-I-III (Baseline)
|
42 score on a scale
Interval 35.5 to 52.5
|
42 score on a scale
Interval 38.5 to 49.25
|
37 score on a scale
Interval 36.0 to 39.0
|
|
Measuring the Effects of K0706 on Motor Function by Using the Unified Parkinson's Disease Rating Scale (UPDRS)-I-III.
UPDRS-I-III (EOT)
|
54 score on a scale
Interval 34.5 to 63.5
|
45 score on a scale
Interval 37.25 to 49.25
|
45.5 score on a scale
Interval 41.25 to 47.25
|
OTHER_PRE_SPECIFIED outcome
Timeframe: 12 weeksPopulation: Median and Interquartile Range (IQR) are robust, non-parametric statistics used to describe central tendency and dispersion when outliers are present. The median represents the 50th percentile, while the IQR measures the spread of the middle 50% of the data. The number shown is the median value, not the mean value.
Timed Up and Go (TUG) is an assessment of mobility, balance, walking ability, and fall risk. It measures the time that a person takes to rise from a chair, walk three meters, turn around, walk back to the chair, and sit down. This assessment is measured in seconds. A score of less than 10 seconds is normal, 14-20 seconds indicates a high fall risk or frailty, and over 30 seconds suggests significant mobility impairment.
Outcome measures
| Measure |
Placebo Powder
n=7 Participants
Placebo: Ten (10) patients in group 1 received the sachet of matching placebo (equivalent to a capsule of placebo "sugar pill") orally daily for 12 weeks (90 days) without food.
|
192 mg Powder of K0706
n=10 Participants
192 mg powder of K0706: Ten (10) patients in group 2 received the sachet of 192 mg powder of K0706 (equivalent to 96 mg capsule of K0706) orally for 12 weeks (90 days) without food.
|
384 mg Powder of K0706
n=3 Participants
384 mg powder of K0706: Nine (9) patients in group 3 received the 384 mg powder of K0706 (equivalent to 192 capsule of K0706) orally daily for 12 weeks (90 days) without food.
|
|---|---|---|---|
|
Measuring the Effects of K0706 on Motor Function by Using the Timed-Up-And-Go (TUG).
TUG
|
-1 seconds
Interval -1.5 to 0.5
|
-1.5 seconds
Interval -2.75 to 1.25
|
-1 seconds
Interval -1.0 to 2.0
|
|
Measuring the Effects of K0706 on Motor Function by Using the Timed-Up-And-Go (TUG).
TUG (Baseline)
|
11 seconds
Interval 10.0 to 15.0
|
13 seconds
Interval 10.5 to 15.75
|
12.5 seconds
Interval 11.75 to 13.25
|
|
Measuring the Effects of K0706 on Motor Function by Using the Timed-Up-And-Go (TUG).
TUG (EOT)
|
11 seconds
Interval 11.0 to 13.5
|
12 seconds
Interval 11.0 to 14.5
|
13.5 seconds
Interval 12.25 to 14.75
|
Adverse Events
Placebo Powder
192 mg Powder of K0706
384 mg Powder of K0706
Serious adverse events
| Measure |
Placebo Powder
n=10 participants at risk
Placebo: Ten (10) patients in group 1 received the sachet of matching placebo (equivalent to a capsule of placebo "sugar pill") orally daily for 12 weeks (90 days) without food.
|
192 mg Powder of K0706
n=10 participants at risk
192 mg powder of K0706: Ten (10) patients in group 2 received the sachet of 192 mg powder of K0706 (equivalent to 96 mg capsule of K0706) orally for 12 weeks (90 days) without food.
|
384 mg Powder of K0706
n=9 participants at risk
384 mg powder of K0706: Nine (9) patients in group 3 received the 384 mg powder of K0706 (equivalent to 192 capsule of K0706) orally daily for 12 weeks (90 days) without food.
|
|---|---|---|---|
|
Cardiac disorders
congestive heart failure and aspiration pneumonia
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
11.1%
1/9 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
Other adverse events
| Measure |
Placebo Powder
n=10 participants at risk
Placebo: Ten (10) patients in group 1 received the sachet of matching placebo (equivalent to a capsule of placebo "sugar pill") orally daily for 12 weeks (90 days) without food.
|
192 mg Powder of K0706
n=10 participants at risk
192 mg powder of K0706: Ten (10) patients in group 2 received the sachet of 192 mg powder of K0706 (equivalent to 96 mg capsule of K0706) orally for 12 weeks (90 days) without food.
|
384 mg Powder of K0706
n=9 participants at risk
384 mg powder of K0706: Nine (9) patients in group 3 received the 384 mg powder of K0706 (equivalent to 192 capsule of K0706) orally daily for 12 weeks (90 days) without food.
|
|---|---|---|---|
|
General disorders
Pain
|
20.0%
2/10 • Number of events 2 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
20.0%
2/10 • Number of events 2 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Gastrointestinal disorders
Diarrhea
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Gastrointestinal disorders
Gastritis
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
General disorders
Nausea/Vomiting
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
11.1%
1/9 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Blood and lymphatic system disorders
Elevated amylase
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Blood and lymphatic system disorders
Hypophosphatemia
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Blood and lymphatic system disorders
Anemia
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
11.1%
1/9 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Blood and lymphatic system disorders
Leukopenia
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
General disorders
COVID-19
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
11.1%
1/9 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
General disorders
Changes in Gait
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Eye disorders
Cataract
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
General disorders
Swelling
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Psychiatric disorders
Hallucinations
|
20.0%
2/10 • Number of events 3 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Psychiatric disorders
Anxiety
|
20.0%
2/10 • Number of events 2 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Renal and urinary disorders
Urinary tract infection
|
10.0%
1/10 • Number of events 2 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Blood and lymphatic system disorders
Elevated lipase
|
10.0%
1/10 • Number of events 2 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
General disorders
Falls
|
40.0%
4/10 • Number of events 28 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
50.0%
5/10 • Number of events 6 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Skin and subcutaneous tissue disorders
Lesions
|
20.0%
2/10 • Number of events 2 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
20.0%
2/10 • Number of events 3 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Injury, poisoning and procedural complications
Fracture
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Nervous system disorders
Alertness
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Nervous system disorders
Insomnia
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Nervous system disorders
Confusion
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Nervous system disorders
Lethargy
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
11.1%
1/9 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Nervous system disorders
Sciatica
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Psychiatric disorders
Paranoia
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Respiratory, thoracic and mediastinal disorders
Upper respiratory infections
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
11.1%
1/9 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Respiratory, thoracic and mediastinal disorders
Asthma
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Respiratory, thoracic and mediastinal disorders
Episodic cardiopulmonary exertion
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Skin and subcutaneous tissue disorders
Skin tags
|
10.0%
1/10 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/9 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
|
Skin and subcutaneous tissue disorders
Cellulitis
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
0.00%
0/10 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
11.1%
1/9 • Number of events 1 • Adverse events were recorded over the course of sixteen weeks for each participant.
|
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place