LivingGLP1
GIP and GLP-1 receptor co-agonist

Tirzepatide subcutaneous once weekly, maximum tolerated dose: 10 or 15 mg

TIRZ_SC_MTD_QW

Agent
tirzepatide
Route
SC
Frequency
QW
Dosing
maximum tolerated
Mechanism
Dual incretin agonist (tirzepatide and others)
Trials
2
Participants in these arms
662

For example SURMOUNT-5. Sensitivity analysis assigns the arm to 15 mg. A different permitted dose set is a different node.

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 40 to 104 (target week 68)PlaceboMD -9.01 (-19.87 to 2.82)0.91
Overweight or obesity without diabetes (adults)Percent body weight changeweeks 40 to 104 (target week 68)PlaceboMD -23.57 (-29.15 to -12.76)0.93
Overweight or obesity without diabetes (adults)Percent body weight changeweeks 40 to 104 (target week 68)PlaceboMD -20.61 (-25.15 to -15.27)0.99
Overweight or obesity without diabetes (adults)SF-36 physical component summary changeweeks 20 to 130 (target week 52)PlaceboMD 3.93 (-4.38 to 12.06)0.78
Overweight or obesity without diabetes (adults)Serious adverse eventslongest follow-upPlaceboHR 1.20 (0.49 to 2.96)0.49
Overweight or obesity without diabetes (adults)Discontinuation due to adverse eventslongest follow-upPlaceboHR 5.13 (2.10 to 13.78)0.24
Overweight or obesity without diabetes (adults)Nausealongest follow-upPlaceboHR 3.28 (2.11 to 5.14)0.55
Overweight or obesity without diabetes (adults)Vomitinglongest follow-upPlaceboHR 11.19 (4.42 to 32.26)0.18
Overweight or obesity without diabetes (adults)Diarrhealongest follow-upPlaceboHR 3.66 (1.96 to 6.93)0.22
Overweight or obesity without diabetes (adults)Constipationlongest follow-upPlaceboHR 3.40 (1.53 to 7.45)0.28

Trials