In REWIND patients taking metformin at baseline, dulaglutide had a primary cardiovascular outcome hazard ratio of 0.92 versus placebo.
In plain wordsIn patients taking metformin at baseline, the cardiovascular outcome hazard ratio for dulaglutide versus placebo was 0.92.
- Peptide
- Dulaglutide (Trulicity)
- Outcome
- Direction not reportedPrimary CV composite with baseline metformin
- Study
n = 8,037
- Comparator
- Placebo
- Analysis
- Primary
- Outcome group
- Cardiovascular events · Cardiovascular
- Studied dose
- 1.5 mg weekly · subcutaneousAs given in this study (human).
Measurements
- Hazard ratio
- 0.92 ratio
- baseline metformin
- CI lower
- 0.81 ratio
- baseline metformin
- CI upper
- 1.05 ratio
- baseline metformin
Source sentences
There was no significant difference in the effect of dulaglutide on the primary outcome in patients with vs. without metformin at baseline [HR 0.92 (CI 0.81-1.05) vs. 0.78 (CI 0.61-0.99); interaction P = 0.18].
3 context sentences(design, population, supporting numbers)
Patients in REWIND (n = 9901; women: 46.3%; mean age: 66.2 years) had type 2 diabetes and either a previous CV event (31%) or high CV risk (69%).
They were randomized (1:1) to sc. dulaglutide (1.5 mg/weekly) or placebo in addition to standard of care.
The primary outcome was the first of a composite of nonfatal myocardial infarction, nonfatal stroke, and death from cardiovascular or unknown causes.