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. 2021 Dec 2;37(3):513–524. doi: 10.1002/mds.28879

TABLE 1.

Characteristics of participants at baseline

Baseline demographics Placebo (N = 86) 10 mg LY3154207 (N = 86) 30 mg LY3154207 (N = 85) 75 mg LY3154207 (N = 87) Overall (N = 344)
Male, % 81.4 84.9 82.4 82.8 82.8
Age, mean 73.1 72.5 71.9 73.0 72.6
White, % 91.9 94.2 95.3 97.7 94.8
AChEI use, % 44.2 39.5 44.7 41.4 42.4
DLB, % 50.6 38.1 36.6 26.2 37.8*
PDD, % 49.4 61.9 63.4 73.8 62.2*
Concomitant PD therapy use, % 83.7 86.0 83.5 89.7 85.8
LEDD (mg), mean 621.2 610.1 606.9 677.8 629.5

MoCA

Total score, %

Mild 17 , 18 , 19 , 20 , 21 , 22 , 23 68.6 69.8 80.0 69.0 71.8
Moderate 10 , 11 , 12 , 13 , 14 , 15 , 16 31.4 30.2 20.0 31.0 28.2
Clinical characteristics, mean (SD)
CDR‐CoA 28.15 (7.23) 28.84 (7.50) 28.81 (12.15) 28.98 (6.19) 28.70 (8.53)
ADAS‐cog13 27.52 (8.67) 27.77 (11.22) 25.07 (9.42) 26.24 (10.32) 26.65 (9.97)
MDS‐UPDRS
Total 61.77 (24.57) 63.33 (25.19) 64.10 (24.15) 69.44 (23.47) 64.70 (24.41)
Part I 12.45 (6.04) 13.03 (6.32) 13.06 (6.34) 13.00 (4.84) 12.89 (5.89)
Part II 15.92 (9.12) 14.66 (8.39) 15.26 (8.05) 16.78 (7.96) 15.66 (8.39)
Part III 33.14 (14.68) 35.85 (15.72) 35.58 (14.71) 39.35 (15.11) 36.02 (15.16)
ESS 10.88 (5.68) 9.53 (4.82) 9.32 (4.91) 10.17 (5.83) 9.98 (5.35)
MoCA total 18.02 (3.54) 18.19 (3.21) 18.80 (3.00) 17.89 (3.85) 18.22 (3.42)
Modified H&Y 2.53 (0.75) 2.42 (0.67) 2.51 (0.67) 2.56 (0.80) 2.51 (0.72)
*

P < 0.05.

Abbreviations: N, number of participants; AChEI, acetylcholinesterase inhibitor; DLB, dementia with Lewy bodies; PDD, Parkinson's disease dementia; PD, Parkinson disease; LEDD, levodopa equivalent daily dose; MoCA, Montreal Cognitive Assessment; SD, standard deviation; CDR‐CoA, Cognitive Drug Research‐Continuity of Attention composite score; ADAS‐cog13, Alzheimer's Disease Assessment Scale‐Cognitive Subscale 13; MDS‐UPDRS, Movement Disorder Society‐Unified Parkinson Disease Rating Scale; ESS, Epworth Sleepiness Scale; H&Y, Hoehn and Yahr.