Obesity

Tirzepatide for the treatment of obesity: Rationale and design of the SURMOUNT clinical development program

Obesity (Silver Spring)Published Rationale and design of a phase 3 clinical development program

Authors' conclusion

The extensive assessment of once-weekly tirzepatide in the global SURMOUNT program will detail the clinical effects of this first-in-class glucose-dependent insulinotropic polypeptide and glucagon-like peptide-1 receptor agonist in chronic weight management.

Study context

Population
Adults with BMI ≥ 27 kg/m² with or without T2D4 trials
Comparison
Once-weekly subcutaneous tirzepatide vs placebo, adjunct to lifestyle intervention
Primary endpoint
Percentage change in body weight
Follow-up
Randomization to end of treatment
Methodological detailsfour randomised controlled trials, global, double-blind, placebo-controlled
  • Four randomised controlled trials
  • Global
  • Double-blind
  • Placebo-controlled

Primary result

As reported in the abstract

Baseline characteristics across trials

Mean age

44.9 to 54.2 years

Female

50.7% to 69.7%

Mean BMI

36.1 to 38.9

Original publication

Tirzepatide for the treatment of obesity: Rationale and design of the SURMOUNT clinical development program. Obesity (Silver Spring). Published 7 December 2022. doi:10.1002/oby.23612

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