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Table 4 Summary of participants with worsening any time postdose on individual domains of the Neuropsychiatric Inventory

From: Further analyses of the safety of verubecestat in the phase 3 EPOCH trial of mild-to-moderate Alzheimer’s disease

Domain

12 mg, n/m (%)

40 mg, n/m (%)

Placebo, n/m (%)

Delusions

135/633 (21.3)

124/632 (19.6)

153/639 (23.9)

Hallucinations

84/633 (13.3)

89/632 (14.1)

79/639 (12.4)

Agitation/aggression

245/633 (38.7)

258/632 (40.8)

259/639 (40.5)

Depression/dysphoria

278/633 (43.9)

333/632 (52.7)

256/639 (40.1)

Anxiety

269/633 (42.5)

270/632 (42.7)

250/639 (39.1)

Elation/euphoria

66/633 (10.4)

60/632 (9.5)

62/639 (9.7)

Apathy/indifference

294/633 (46.4)

297/632 (47.0)

306/639 (47.9)

Disinhibition

159/633 (25.1)

155/632 (24.5)

128/639 (20.0)

Irritability/lability

244/633 (38.5)

284/632 (44.9)

244/639 (38.2)

Aberrant motor behavior

177/633 (28.0)

188/632 (29.7)

198/639 (31.0)

Sleep and nighttime behavior disorders

191/633 (30.2)

225/632 (35.6)

182/639 (28.5)

Appetite and eating changes

252/632 (39.9)

255/631 (40.4)

225/639 (35.2)

  1. Worsening was determined by comparing the postdose score to the baseline score
  2. n/m = number of participants with the given item present at that time point/number of participants measured at that time point