← 홈

프로그램 비교

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

현재 선택: 2 · 차세대 보드에서 열림

프로그램 상세에서 관심 등록 후 2개 이상 모으면 여기서 한 번에 비교할 수 있습니다.

API CSV32행 · 2개 프로그램

표가 넓으면 좌우로 스크롤하세요. 핵심 비교 모드에서는 중요 항목만 표시됩니다.

항목
AntibodyCurated CoreFDAApproved
semaglutide (Ozempic / Wegovy, GLP-1, Wegovy, NN9535)
Novo Nordisk·GLP-1 receptor
410 trials·t½ 168 days
AntibodyCurated CoreFDAApproved
tirzepatide (Mounjaro / Zepbound, Mounjaro, Zepbound, LY3298176)
Eli Lilly·GLP-1 / GIP receptor
269 trials·t½ 5 h
Overview
Program
Ozempic / Wegovy (semaglutide)Mounjaro / Zepbound (tirzepatide)
Overview
Company
Novo NordiskEli Lilly
Overview
Modality
ANTIBODYANTIBODY
Overview
Target
GLP-1 receptorGLP-1 / GIP receptor
Overview
Indication
Type 2 diabetes, chronic weight management, CV risk reduction (T2D)Type 2 diabetes, chronic weight management
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
Weekly SC (Ozempic/Wegovy) and oral form (Rybelsus)Dual incretin mechanism vs GLP-1-only agonists
Positioning
Known limitation
GI intolerance leading to discontinuation; plateau after dose titrationGI side effects during titration; individualized dose escalation required.
Positioning
Development positioning
GLP-1 class anchor vs tirzepatide dual agonist
MoA
Mechanism
Semaglutide activates GLP-1 receptors on pancreatic beta cells (glucose-dependent insulin secretion), suppresses glucagon, slows gastric emptying, and reduces appetite via central pathways.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.
MoA
Biomarker
HbA1c, body weight, SELECT CV outcomes in obesity with CVD.HbA1c, body weight, lipids.
PK/PD
Half-life
168 days5 h
PK/PD
Species
Rat, HbA1c ↓1.5–1.8%, weight ↓~15% at 68 wk (STEP-1)Mouse, HbA1c ↓2.0%+
PK/PD
Animal (cat.)
RatMouse
PK/PD
Experiment
PKpharmacokinetic
Toxicology
Species
NHP, Mouse, RatMouse, Rat
Toxicology
Animal (cat.)
NHP
Toxicology
Major finding
Thyroid C-cell tumors in rodents (class warning); GI AEs in clinicGI events (nausea, diarrhea) most common; gallbladder disease; thyroid C-cell rodent findings.
Toxicology
CRS
N/AN/A
Clinical
Safety signal
Thyroid C-cell tumors in rodents (class warning); GI AEs in clinicGI events (nausea, diarrhea) most common; gallbladder disease; thyroid C-cell rodent findings.
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