LivingGLP1
GIP; GLP-1 and glucagon receptor tri-agonist

Retatrutide 4 mg subcutaneous once weekly

RETA_SC_4MG_QW

Agent
retatrutide
Route
SC
Dose
4 mg
Frequency
QW
Dosing
fixed
Mechanism
Triple agonist (retatrutide; efocipegtrutide; UBT251 and others)
Trials
1
Participants in these arms
33

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
Type 2 diabetes (adults)Serious adverse eventslongest follow-upPlaceboHR 1.27 (0.25 to 5.17)0.41
Type 2 diabetes (adults)Nausealongest follow-upPlaceboHR 2.94 (1.03 to 7.94)0.46
Type 2 diabetes (adults)Vomitinglongest follow-upPlaceboHR 0.55 (0.04 to 3.39)0.82
Type 2 diabetes (adults)Constipationlongest follow-upPlaceboHR 3.57 (1.00 to 12.20)0.23
Overweight or obesity without diabetes (adults)Percent body weight changeweeks 20 to 40 (target week 26)PlaceboMD -10.94 (-16.13 to -3.29)0.79
Overweight or obesity without diabetes (adults)Percent body weight changeweeks 40 to 104 (target week 68)PlaceboMD -13.96 (-20.16 to -3.82)0.49
Overweight or obesity without diabetes (adults)Serious adverse eventslongest follow-upPlaceboHR 0.67 (0.10 to 3.71)0.64
Overweight or obesity without diabetes (adults)Nausealongest follow-upPlaceboHR 2.38 (1.06 to 5.70)0.68
Overweight or obesity without diabetes (adults)Vomitinglongest follow-upPlaceboHR 4.47 (1.15 to 21.20)0.48
Overweight or obesity without diabetes (adults)Diarrhealongest follow-upPlaceboHR 1.02 (0.35 to 2.95)0.74
Overweight or obesity without diabetes (adults)Constipationlongest follow-upPlaceboHR 2.70 (0.70 to 11.83)0.39

Trials