Table 1

Baseline characteristics and subject disposition of subjects with onset of nausea/vomiting from baseline to week 12 and at any time from baseline to end of treatment (yes/no) in the SUSTAIN 3, 7 and 10 trials

TreatmentSemaglutide 0.5 mg (SUSTAIN 7)Semaglutide 1.0 mg (pooled)Exenatide ER 2.0 mg (SUSTAIN 3)Dulaglutide 0.75 mg (SUSTAIN 7)Dulaglutide 1.5 mg (SUSTAIN 7)Liraglutide 1.2 mg (SUSTAIN 10)
N (total)301994405299299287
Nausea/vomiting Yes/NoYNYNYNYNYNYN
Baseline to week 12
N7123021378150355372626323654233
Race, n (%)
 Asian15 (21.1)35 (15.2)13 (6.1)38 (4.9)1 (2.0)5 (1.4)7 (18.9)41 (15.6)11 (17.5)44 (18.6)0 (0.0)3 (1.3)
 Black or African American3 (4.2)14 (6.1)11 (5.2)37 (4.7)2 (4.0)28 (7.9)0 (0.0)17 (6.5)2 (3.2)16 (6.8)0 (0.0)1 (0.4)
 White53 (74.6)180 (78.3)179 (84.0)669 (85.7)44 (88.0)294 (82.8)30 (81.1)202 (77.1)48 (76.2)172 (72.9)49 (90.7)219 (94.0)
 Other0 (0.0)1 (0.4)10 (4.7)37 (4.7)3 (6.0)28 (7.9)0 (0.0)2 (0.8)2 (3.2)4 (1.7)5 (9.3)10 (4.3)
Ethnic group, n (%)
 Hispanic or Latino8 (11.3)21 (9.1)25 (11.7)107 (13.7)11 (22.0)95 (26.8)4 (10.8)27 (10.3)11 (17.5)32 (13.6)1 (1.9)2 (0.9)
 Not Hispanic or Latino63 (88.7)209 (90.9)185 (86.9)661 (84.6)39 (78.0)260 (73.2)33 (89.2)235 (89.7)52 (82.5)204 (86.4)48 (88.9)221 (94.8)
 Other0 (0.0)0 (0.0)3 (1.4)13 (1.7)0 (0.0)0 (0.0)0 (0.0)0 (0.0)0 (0.0)0 (0.0)5 (9.3)10 (4.3)
Baseline HbA1c, %8.3 (1.0)8.3 (1.0)8.2 (0.9)8.3 (0.9)8.4 (1.1)8.3 (0.9)8.2 (0.9)8.2 (0.9)8.2 (0.8)8.2 (0.9)8.2 (1.0)8.3 (1.0)
Baseline BMI, kg/m232.5 (7.2)34.0 (7.1)33.1 (6.3)34.0 (7.0)32.7 (6.2)33.7 (6.2)35.3 (6.5)33.4 (6.9)32.3 (6.9)33.3 (6.5)33.0 (7.8)33.8 (6.8)
Baseline BW, kg92.1 (28.4)97.7 (22.9)92.4 (19.4)97.1 (22.0)90.2 (16.7)96.1 (20.9)98.7 (22.9)95.2 (23.0)89.7 (21.9)94.4 (21.7)93.3 (25.2)98.1 (20.8)
Exposure time, years0.7 (0.3)0.8 (0.2)0.7 (0.3)0.9 (0.3)1.0 (0.4)1.0 (0.3)0.8 (0.1)0.8 (0.1)0.7 (0.3)0.8 (0.2)0.6 (0.2)0.6 (0.1)
Duration of diabetes, years7.4 (5.9)7.8 (5.9)8.8 (6.5)8.7 (5.9)9.6 (7.2)9.4 (6.6)7.0 (5.2)7.0 (5.5)7.1 (5.4)7.8 (5.7)8.2 (5.0)9.1 (5.8)
Onset of rescue, n (%)0 (0.0)3 (1.3)3 (1.4)36 (4.6)3 (6.0)45 (12.7)2 (5.4)12 (4.6)0 (0.0)7 (3.0)1 (1.9)11 (4.7)
Discontinued treatment, n (%)21 (29.6)26 (11.3)61 (28.6)111 (14.2)12 (24.0)73 (20.6)3 (8.1)24 (9.2)15 (23.8)21 (8.9)10 (18.5)16 (6.9)
Withdrawal from trial, n (%)5 (7.0)17 (7.4)17 (8.0)37 (4.7)6 (12.0)30 (8.5)1 (2.7)12 (4.6)3 (4.8)12 (5.1)2 (3.7)3 (1.3)
Lost to follow-up, n (%)3 (4.2)6 (2.6)9 (4.2)13 (1.7)2 (4.0)8 (2.3)0 (0.0)8 (3.1)1 (1.6)7 (3.0)1 (1.9)2 (0.9)
At any time from baseline to EOT
N7622524574957348482516923057230
Race, n (%)
 Asian16 (21.1)34 (15.1)14 (5.7)37 (4.9)1 (1.8)5 (1.4)8 (16.7)40 (15.9)12 (17.4)43 (18.7)0 (0.0)3 (1.3)
 Black or African American4 (5.3)13 (5.8)13 (5.3)35 (4.7)2 (3.5)28 (8.0)1 (2.1)16 (6.4)4 (5.8)14 (6.1)0 (0.0)1 (0.4)
 White56 (73.7)177 (78.7)207 (84.5)641 (85.6)51 (89.5)287 (82.5)39 (81.3)193 (76.9)51 (73.9)169 (73.5)51 (89.5)217 (94.3)
 Other0 (0.0)1 (0.4)11 (4.5)36 (4.8)3 (5.3)28 (8.0)0 (0.0)2 (0.8)2 (2.9)4 (1.7)6 (10.5)9 (3.9)
Ethnic group, n (%)
 Hispanic or Latino8 (10.5)21 (9.3)26 (10.6)106 (14.2)11 (19.3)95 (27.3)4 (8.3)27 (10.8)11 (15.9)32 (13.9)1 (1.8)2 (0.9)
 Not Hispanic or Latino68 (89.5)204 (90.7)216 (88.2)630 (84.1)46 (80.7)253 (72.7)44 (91.7)224 (89.2)58 (84.1)198 (86.1)50 (87.7)219 (95.2)
 Other0 (0.0)0 (0.0)3 (1.2)13 (1.7)0 (0.0)0 (0.0)0 (0.0)0 (0.0)0 (0.0)0 (0.0)6 (10.5)9 (3.9)
Baseline HbA1c, %8.3 (1.0)8.3 (1.0)8.2 (0.9)8.3 (0.9)8.4 (1.1)8.3 (0.9)8.1 (0.9)8.2 (0.9)8.1 (0.8)8.2 (0.9)8.2 (1.0)8.3 (1.0)
Baseline BMI, kg/m232.9 (7.6)33.9 (6.9)33.4 (6.7)33.9 (6.9)33.0 (6.4)33.7 (6.2)34.6 (6.7)33.5 (6.9)32.3 (6.8)33.3 (6.5)33.4 (8.0)33.7 (6.7)
Baseline BW, kg92.8 (28.2)97.6 (22.9)93.4 (20.4)97.0 (21.9)91.0 (16.1)96.1 (21.0)97.3 (24.0)95.3 (22.8)89.8 (21.3)94.5 (21.9)94.0 (25.2)98.0 (20.7)
Exposure time, years0.7 (0.3)0.8 (0.2)0.8 (0.3)0.9 (0.3)1.0 (0.4)1.0 (0.3)0.8 (0.1)0.8 (0.1)0.7 (0.3)0.8 (0.2)0.6 (0.2)0.6 (0.1)
Duration of diabetes, years7.3 (5.8)7.9 (6.0)8.9 (6.5)8.6 (5.8)9.5 (7.1)9.4 (6.7)7.1 (5.4)7.0 (5.5)7.4 (5.8)7.7 (5.6)8.6 (5.2)9.0 (5.8)
Onset of rescue, n (%)0 (0.0)3 (1.3)3 (1.2)36 (4.8)3 (5.3)45 (12.9)2 (4.2)12 (4.8)0 (0.0)7 (3.0)1 (1.8)11 (4.8)
Discontinued treatment, n (%)21 (27.6)26 (11.6)67 (27.3)105 (14.0)13 (22.8)72 (20.7)5 (10.4)22 (8.8)15 (21.7)21 (9.1)10 (17.5)16 (7.0)
Withdrawal from trial, n (%)5 (6.6)17 (7.6)19 (7.8)35 (4.7)6 (10.5)30 (8.6)2 (4.2)11 (4.4)3 (4.3)12 (5.2)2 (3.5)3 (1.3)
Lost to follow-up, n (%)3 (3.9)6 (2.7)9 (3.7)13 (1.7)2 (3.5)8 (2.3)1 (2.1)7 (2.8)1 (1.4)7 (3.0)1 (1.8)2 (0.9)
  • Data are mean (standard deviation) unless otherwise specified. Only subjects with non-missing subgroup information were selected.

  • AE, adverse event; BMI, body mass index; BW, body weight; EOT, end of treatment; exenatide ER, exenatide extended release; GI, gastrointestinal; HbA1c, glycated hemoglobin.