Table 3

Summary of TEAE occurring in ≥5% of patients across the non-inferiority and extension studies (safety analysis set)

EventLansoprazole 15 mg (n=210)Vonoprazan 10 mg (n=218)Vonoprazan 20 mg (n=212)Statistical test
Events, nPatients, n (%)Events, nPatients, n (%)Events, nPatients, n (%)
Summary of AEsΧ2 test
 Any AE634185
(88.1)
758184
(84.4)
731175
(82.5)
p=0.2673
 Drug-related AE4440
(19.0)
5238
(17.4)
5137
(17.5)
p=0.8839
 Leading to study discontinuation1716
(7.6)
99
(4.1)
3227
(12.7)
p=0.0046
 Any serious AE*2018
(8.6)
2218
(8.3)
3630
(14.2)
p=0.0796
 Serious drug-related AE†00
(0)
22
(0.9)
22
(0.9)
p=0.3740
 Special interest AE‡22
(1.0)
55
(2.3)
43
(1.4)
p=0.5232
 Drug-related special interest AE11
(0.5)
22
(0.9)
00
(0)
p=0.3792
TEAEs reported in ≥5% of patients in any treatment group by preferred term, n (%)
 Nasopharyngitis61 (29.0)70 (32.1)59 (27.8)
 Fall18 (8.6)22 (10.1)18 (8.5)
 Contusion20 (9.5)17 (7.8)14 (6.6)
 Diarrhoea14 (6.7)11 (5.0)15 (7.1)
 Upper respiratory tract inflammation7 (3.3)12 (5.5)14 (6.6)
 Seasonal allergy8 (3.8)8 (3.7)15 (7.1)
 Eczema12 (5.7)10 (4.6)8 (3.8)
 Elevated blood creatine phosphokinase11 (5.2)9 (4.1)7 (3.3)
 Constipation5 (2.4)15 (6.9)7 (3.3)
 Back pain6 (2.9)7 (3.2)13 (6.1)
 Contact dermatitis6 (2.9)8 (3.7)12 (5.7)
 Stomatitis7 (3.3)11 (5.0)4 (1.9)
 Dental caries11 (5.2)6 (2.8)4 (1.9)
  • *Serious AE.

  • †Serious drug-related AE: putamen haemorrhage.

  • ‡Special interest AE: liver function test abnormal.

  • AE, adverse event; TEAE, treatment-emergent AE.