LivingGLP1
Long acting GLP-1 receptor agonist (injectable)

Efpeglenatide 6 mg injection every 2 weeks

EFPE_SC_6MG_Q2W

Effects across outcomes

Bayesian random effects estimate against the comparator of each analysis (usually placebo), posterior median and 95% credible interval. Green: clearly better; red: clearly worse.
ConditionOutcomeWindowVersusEffect (95% CrI)SUCRA
Overweight or obesity without diabetes (adults)Systolic blood pressure changeweeks 20 to 40 (target week 26)PlaceboMD -0.04 (-9.47 to 9.54)0.22
Overweight or obesity without diabetes (adults)Percent body weight changeweeks 20 to 40 (target week 26)PlaceboMD -6.19 (-13.27 to 2.36)0.38
Overweight or obesity without diabetes (adults)Weight loss of 5 percent or moreweeks 20 to 40 (target week 26)PlaceboOR 10.41 (1.04 to 45.90)0.48
Overweight or obesity without diabetes (adults)Weight loss of 10 percent or moreweeks 20 to 40 (target week 26)PlaceboOR 5.67 (0.88 to 29.64)0.41
Overweight or obesity without diabetes (adults)Serious adverse eventslongest follow-upPlaceboHR 0.23 (0.00 to 5.66)0.76
Overweight or obesity without diabetes (adults)Discontinuation due to adverse eventslongest follow-upPlaceboHR 1.67 (0.50 to 5.89)0.54
Overweight or obesity without diabetes (adults)Nausealongest follow-upPlaceboHR 2.95 (1.47 to 6.22)0.60
Overweight or obesity without diabetes (adults)Vomitinglongest follow-upPlaceboHR 2.21 (0.77 to 7.16)0.71
Overweight or obesity without diabetes (adults)Diarrhealongest follow-upPlaceboHR 1.30 (0.54 to 3.25)0.66
Overweight or obesity without diabetes (adults)Constipationlongest follow-upPlaceboHR 1.71 (0.52 to 5.70)0.56
Overweight or obesity without diabetes (adults)Discontinuation due to gastrointestinal adverse eventslongest follow-upPlaceboHR 2.29 (0.43 to 13.14)0.48

Trials