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Table 2 Summary of study population for all entered patients

From: A double-blind, placebo-controlled comparator study of LY2140023 monohydrate in patients with schizophrenia

Analysis Population

PBO n (%) a

LY40 n (%) a

LY80 n (%) a

RIS n (%) a

Total n (%) a

Randomized Patients

N = 295

N = 293

N = 282

N = 143

N = 1013

Completed

171 (58.0)

143 (48.8)

129 (45.7)

96 (67.1)

539 (53.2)

ITT Patients in the Overall Population

295 (100.0)

292 (99.7)

280 (99.3)

142 (99.3)

1009 (99.6)

Completed

171 (58.0)

143 (48.8)

129 (45.7)

96 (67.1)

539 (53.2)

Efficacy-Evaluable ITT Patients in the Overall Population

267 (90.5)

267 (91.1)

253 (89.7)

132 (92.3)

919 (90.7)

Completed

154 (52.2)

136 (46.4)

116 (41.1)

90 (62.9)

496 (49.0)

ITT Patients in the Predefined Subpopulation

211 (71.5)

210 (71.7)

195 (69.1)

98 (68.5)

714 (70.5)

Completed

120 (40.7)

107 (36.5)

83 (29.4)

65 (45.5)

375 (37.0)

Efficacy-Evaluable ITT Patients in the Predefined Subpopulation

195 (66.1)

189 (64.5)

176 (62.4)

93 (65.0)

653 (64.5)

Completed

111 (37.6)

101 (34.5)

73 (25.9)

61 (42.7)

346 (34.2)

  1. aPercentages were calculated based on all randomized patients per group.
  2. Abbreviations: ITT intent-to-treat, N/n number of patients.
  3. Groups: PBO = placebo; LY40 = LY2140023 monohydrate 40 mg; LY80 = LY2140023 monohydrate 80 mg; RIS = risperidone.