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타깃 · 모달리티 · 임상 근거 · 비임상 맥락으로 최대 5개 프로그램을 나란히 비교합니다. · 다음 갱신 D-6 · 마지막 9월 2일

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API CSV32행 · 2개 프로그램

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항목
AntibodyCurated CoreFDAApproved
tirzepatide (Mounjaro / Zepbound, Mounjaro, Zepbound, LY3298176)
Eli Lilly·GLP-1 / GIP receptor
269 trials·t½ 5 h
AntibodyCurated CoreFDAApproved
semaglutide (Ozempic / Wegovy, GLP-1, Wegovy, NN9535)
Novo Nordisk·GLP-1 receptor
410 trials·t½ 168 days
Overview
Program
Mounjaro / Zepbound (tirzepatide)Ozempic / Wegovy (semaglutide)
Overview
Company
Eli LillyNovo Nordisk
Overview
Modality
ANTIBODYANTIBODY
Overview
Target
GLP-1 / GIP receptorGLP-1 receptor
Overview
Indication
Type 2 diabetes, chronic weight managementType 2 diabetes, chronic weight management, CV risk reduction (T2D)
Overview
Phase
APPROVEDAPPROVED
Overview
Status
APPROVEDAPPROVED
Overview
Content status
Curated CoreCurated Core
Overview
Data Confidence
Data Confidence · HighData Confidence · High
Overview
Development Signal
Development Signal · EstablishedDevelopment Signal · Established
Overview
Approval status
FDA approvedFDA approved
Positioning
Key differentiator
Dual incretin mechanism vs GLP-1-only agonistsWeekly SC (Ozempic/Wegovy) and oral form (Rybelsus)
Positioning
Known limitation
GI side effects during titration; individualized dose escalation required.GI intolerance leading to discontinuation; plateau after dose titration
Positioning
Development positioning
GLP-1 class anchor vs tirzepatide dual agonist
MoA
Mechanism
Tirzepatide is a 39-amino-acid peptide activating both GIP and GLP-1 receptors, enhancing insulin secretion, reducing glucagon, slowing gastric emptying, and promoting weight loss via combined incretin effects.Semaglutide activates GLP-1 receptors on pancreatic beta cells (glucose-dependent insulin secretion), suppresses glucagon, slows gastric emptying, and reduces appetite via central pathways.
MoA
Biomarker
HbA1c, body weight, lipids.HbA1c, body weight, SELECT CV outcomes in obesity with CVD.
PK/PD
Half-life
5 h168 days
PK/PD
Species
Mouse, HbA1c ↓2.0%+Rat, HbA1c ↓1.5–1.8%, weight ↓~15% at 68 wk (STEP-1)
PK/PD
Animal (cat.)
MouseRat
PK/PD
Experiment
pharmacokineticPK
Toxicology
Species
Mouse, RatNHP, Mouse, Rat
Toxicology
Animal (cat.)
NHP
Toxicology
Major finding
GI events (nausea, diarrhea) most common; gallbladder disease; thyroid C-cell rodent findings.Thyroid C-cell tumors in rodents (class warning); GI AEs in clinic
Toxicology
CRS
N/AN/A
Clinical
Safety signal
GI events (nausea, diarrhea) most common; gallbladder disease; thyroid C-cell rodent findings.Thyroid C-cell tumors in rodents (class warning); GI AEs in clinic
Clinical
Selected reported efficacy
Weight 1.01%
Clinical
Weight %
weight loss is essential but difficult
Clinical
Result source
ClinicalTrials.gov NCT03480022
Clinical
Program phase
APPROVEDAPPROVED
Clinical
Trial activity
No active/completed countsNo active/completed counts
Clinical
Trial ref
NCT03480022
Preclinical
Animal (cat.)
MouseMouse