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Database

Obesity and peptide drug database

Every compound we track, with its main trial result. Tap a column to sort; tap a name for the full profile.

TirzepatideZepbound / Mounjaro · Eli LillyGIP/GLP-1 dual agonistInjection, weeklyFDA approved22.5%726.2%8.8
RetatrutideNo brand yet · Eli LillyGIP/GLP-1/glucagon triple agonistInjection, weeklyPhase 3 complete28.3%8011.3%6.6
CagriSemaNo brand yet · Novo NordiskAmylin + GLP-1 combinationInjection, weeklyUnder FDA review22.7%686.0%5.2
Oral semaglutide 25 mg*Wegovy pill · Novo NordiskGLP-1 receptor agonistOral, dailyFDA approved16.6%646.9%4.6
Semaglutide 2.4 mgWegovy · Novo NordiskGLP-1 receptor agonistInjection, weeklyFDA approved16.9%687.0%4.5
OrforglipronFoundayo · Eli LillyNon-peptide GLP-1 agonistOral, dailyFDA approved12.4%7210.3%3.4
Semaglutide 7.2 mgWegovy HD · Novo NordiskGLP-1 receptor agonistInjection, weeklyFDA approved20.7%72n/r–
Liraglutide 3.0 mgSaxenda · Novo NordiskGLP-1 receptor agonistInjection, dailyFDA approved8.0%569.9%–
MazdutideApproved in China · Innovent / Eli LillyGLP-1/glucagon dual agonistInjection, weeklyApproved in China14.8%48n/r–
SurvodutideNo brand yet · Boehringer Ingelheim / ZealandGLP-1/glucagon dual agonistInjection, weeklyPhase 3 complete16.6%7624.5%–
MariTideMaridebart cafraglutide · AmgenGLP-1 agonist + GIP receptor blocker (antibody)Injection, monthlyIn Phase 320.0%5211.0%–
AmycretinNo brand yet · Novo NordiskAmylin/GLP-1 unimolecular agonistInjection or oral, weeklyIn Phase 322.0%36n/r–
EloralintideNo brand yet · Eli LillyAmylin receptor agonistInjection, weeklyIn Phase 320.1%48n/r–
PetrelintideNo brand yet · Zealand Pharma / RocheAmylin receptor agonistInjection, weeklyPhase 3 starting10.7%421.0%–
VK2735No brand yet · Viking TherapeuticsGIP/GLP-1 dual agonistInjection (oral in development), weeklyIn Phase 314.7%13n/r–

Weight loss: top dose, efficacy estimand where reported. Trials differ in length and population; Phase 2 results are not comparable with Phase 3. n/r = not reported.

* Wegovy pill: small trial with dose reductions. OASIS 4 included 307 adults, only about 205 of them on the pill, against 1,961 in STEP 1 for the injection, so its side-effect rates are less reliable. In addition, 18.6% of participants who completed treatment ended on a lower dose than 25 mg, which probably kept some from stopping and lowered the reported 6.9% discontinuation rate. Its ranking against the injection should be treated as provisional.