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

Retatrutide 8 mg subcutaneous once weekly

RETA_SC_8MG_QW

Agent
retatrutide
Route
SC
Dose
8 mg
Frequency
QW
Dosing
fixed
Mechanism
Triple agonist (retatrutide; efocipegtrutide; UBT251 and others)
Trials
0
Participants in these arms
0

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 1.19 (0.25 to 4.90)0.43
Type 2 diabetes (adults)Nausealongest follow-upPlaceboHR 6.63 (2.87 to 16.29)0.18
Type 2 diabetes (adults)Vomitinglongest follow-upPlaceboHR 3.56 (1.05 to 12.10)0.41
Type 2 diabetes (adults)Constipationlongest follow-upPlaceboHR 2.74 (0.73 to 10.11)0.32
Overweight or obesity without diabetes (adults)Percent body weight changeweeks 20 to 40 (target week 26)PlaceboMD -15.47 (-20.43 to -7.77)0.94
Overweight or obesity without diabetes (adults)Percent body weight changeweeks 40 to 104 (target week 68)PlaceboMD -19.69 (-25.53 to -8.93)0.78
Overweight or obesity without diabetes (adults)Serious adverse eventslongest follow-upPlaceboHR 0.97 (0.19 to 4.90)0.55
Overweight or obesity without diabetes (adults)Nausealongest follow-upPlaceboHR 3.73 (1.71 to 8.67)0.47
Overweight or obesity without diabetes (adults)Vomitinglongest follow-upPlaceboHR 6.05 (1.66 to 28.57)0.37
Overweight or obesity without diabetes (adults)Diarrhealongest follow-upPlaceboHR 1.80 (0.71 to 4.85)0.52
Overweight or obesity without diabetes (adults)Constipationlongest follow-upPlaceboHR 2.95 (0.79 to 12.98)0.36

Trials