LivingGLP1
Oral small molecule GLP-1 receptor agonist

HRS-7535 180 mg tablet once daily

HRS7535_PO_180MG_QD

Mechanism
Nonpeptide GLP-1 receptor agonist (orforglipron; danuglipron; lotiglipron; aleniglipron and others)
Trials
1
Participants in these arms
48

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 -2.52 (-13.05 to 8.43)0.42
Overweight or obesity without diabetes (adults)Percent body weight changeweeks 20 to 40 (target week 26)PlaceboMD -6.63 (-12.74 to 0.36)0.57
Overweight or obesity without diabetes (adults)Percent body weight changeweeks 20 to 40 (target week 26)PlaceboMD -5.80 (-12.38 to 1.93)0.42
Overweight or obesity without diabetes (adults)Serious adverse eventslongest follow-upPlaceboHR 2.91 (0.38 to 23.43)0.28
Overweight or obesity without diabetes (adults)Discontinuation due to adverse eventslongest follow-upPlaceboHR 7.24 (0.76 to 82.67)0.21
Overweight or obesity without diabetes (adults)Nausealongest follow-upPlaceboHR 12.56 (4.62 to 43.44)0.09
Overweight or obesity without diabetes (adults)Vomitinglongest follow-upPlaceboHR 11.44 (3.56 to 47.38)0.18
Overweight or obesity without diabetes (adults)Diarrhealongest follow-upPlaceboHR 1.98 (0.64 to 6.64)0.48
Overweight or obesity without diabetes (adults)Constipationlongest follow-upPlaceboHR 1.84 (0.10 to 23.50)0.51
Overweight or obesity without diabetes (adults)Discontinuation due to gastrointestinal adverse eventslongest follow-upPlaceboHR 12.95 (0.80 to 325)0.17

Trials