In adults with obesity or overweight without diabetes or prior ASCVD, predicted 10-year ASCVD risk changed by -23.5% to -16.4% with tirzepatide versus 12.7% with placebo at week 72.
In plain wordsIn adults with obesity or overweight without diabetes, predicted heart disease risk fell more with tirzepatide than with placebo.
- Peptide
- Tirzepatide
- Outcome
- DecreaseRelative change in predicted 10-year ASCVD risk at week 72
- Study
n = 2,461
- Comparator
- Placebo
- Outcome group
- Cardiovascular events · Cardiovascular
- Studied dose
- 5/10/15 mg · 72 weeksAs given in this study (human).
Source sentences
Relative change in risk from baseline to week 72 was greater for tirzepatide (-23.5% to -16.4%) than placebo (12.7%; P < 0.001).
3 context sentences(design, population, supporting numbers)
In participants without a history of ASCVD (N = 2461), the baseline median risk score was low and did not differ across groups (1.5%-1.6%).
SURMOUNT-1, a phase 3 trial, evaluated the efficacy and safety of tirzepatide in adults with body mass index ≥30 or ≥27 kg/m2 and at least one weight-related complication, excluding diabetes.
Participants were randomly assigned to tirzepatide (5/10/15 mg) or placebo.