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ABSTRACT: Aims
This analysis aimed to assess the influence of selected baseline factors on tirzepatide treatment response in Japanese patients with obesity disease.Materials and methods
This was a prespecified subgroup analysis of the SURMOUNT-J trial. Japanese adults with obesity disease, excluding diabetes, were randomised 1:1:1 to receive once-weekly subcutaneous tirzepatide 10 mg, tirzepatide 15 mg, or placebo. Key safety and efficacy outcomes at week 72 were analysed by baseline characteristics, including sex, age (<65, ≥65 years), and body mass index (BMI; <35 kg/m2, ≥35 kg/m2). Post hoc analyses were conducted to examine cardiometabolic parameters by subgroup.Results
Overall, 225 participants were examined (tirzepatide 10 mg: n = 73; tirzepatide 1
SUBMITTER: Yokote K
PROVIDER: S-EPMC12803658 | biostudies-literature | 2026 Feb
REPOSITORIES: biostudies-literature