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

Retatrutide 0.5 mg subcutaneous once weekly

RETA_SC_0p5MG_QW

Agent
retatrutide
Route
SC
Dose
0.5 mg
Frequency
QW
Dosing
fixed
Mechanism
Triple agonist (retatrutide; efocipegtrutide; UBT251 and others)
Trials
1
Participants in these arms
47

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)Systolic blood pressure changeweeks 36 to 64 (target week 52)PlaceboMD -3.22 (-9.21 to 2.93)0.58
Type 2 diabetes (adults)Systolic blood pressure changeweeks 20 to 36 (target week 26)PlaceboMD -5.31 (-10.93 to 0.23)0.73
Type 2 diabetes (adults)Serious adverse eventslongest follow-upPlaceboHR 1.27 (0.26 to 5.29)0.40
Type 2 diabetes (adults)Nausealongest follow-upPlaceboHR 0.64 (0.11 to 2.49)0.82
Type 2 diabetes (adults)Vomitinglongest follow-upPlaceboHR 0.55 (0.05 to 3.16)0.82
Type 2 diabetes (adults)Constipationlongest follow-upPlaceboHR 1.66 (0.34 to 6.71)0.49

Trials