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

현재 선택: 3 · 차세대 보드에서 열림

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API CSV32행 · 3개 프로그램

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항목
AntibodyCurated CoreFDAApproved
semaglutide (Ozempic / Wegovy, GLP-1, Wegovy, NN9535)
Novo Nordisk·GLP-1 receptor
410 trials·t½ 168 days
AntibodyCurated CoreFDAApproved
dupilumab (Dupixent, REGN668)
Sanofi / Regeneron·IL-4Rα
278 trials·t½ ~14 days (300 mg q2w)
AntibodyCurated CoreFDAApproved
tirzepatide (Mounjaro / Zepbound, Mounjaro, Zepbound, LY3298176)
Eli Lilly·GLP-1 / GIP receptor
269 trials·t½ 5 h
Overview
Program
Ozempic / Wegovy (semaglutide)Dupixent (dupilumab)Mounjaro / Zepbound (tirzepatide)
Overview
Company
Novo NordiskSanofi / RegeneronEli Lilly
Overview
Modality
ANTIBODYANTIBODYANTIBODY
Overview
Target
GLP-1 receptorIL-4RαGLP-1 / GIP receptor
Overview
Indication
Type 2 diabetes, chronic weight management, CV risk reduction (T2D)Atopic dermatitis, asthma, CRSwNP, EoE, prurigo nodularisType 2 diabetes, chronic weight management
Overview
Phase
APPROVEDAPPROVEDAPPROVED
Overview
Status
APPROVEDAPPROVEDAPPROVED
Overview
Content status
Curated CoreCurated CoreCurated Core
Overview
Data Confidence
Data Confidence · HighData Confidence · HighData Confidence · High
Overview
Development Signal
Development Signal · EstablishedDevelopment Signal · EstablishedDevelopment Signal · Established
Overview
Approval status
FDA approvedFDA approvedFDA approved
Positioning
Key differentiator
Weekly SC (Ozempic/Wegovy) and oral form (Rybelsus)Novel targets under investigation include MRGPRs, PARs, KIT receptors, OX-40, and sodium channelsDual incretin mechanism vs GLP-1-only agonists
Positioning
Known limitation
GI intolerance leading to discontinuation; plateau after dose titrationNon-Type 2 inflammation and inadequate trough levels.GI 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.Dupilumab binds IL-4Rα subunit shared by IL-4 type I and IL-13 type II receptors, inhibiting IL-4 and IL-13 signaling, reducing Type 2 inflammation (IgE, eosinophils, Th2 cytokines).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.biomarkers and clinical characteristics and highlight the need for standardized, methodologically rigorous fuHbA1c, body weight, lipids.
PK/PD
Half-life
168 days~14 days (300 mg q2w)5 h
PK/PD
Species
Rat, HbA1c ↓1.5–1.8%, weight ↓~15% at 68 wk (STEP-1)Mouse, EASI-75, peak pruritus NRS reductionMouse, HbA1c ↓2.0%+
PK/PD
Animal (cat.)
RatMouseMouse
PK/PD
Experiment
PKPDpharmacokinetic
Toxicology
Species
NHP, Mouse, RatMouseMouse, Rat
Toxicology
Animal (cat.)
NHP
Toxicology
Major finding
Thyroid C-cell tumors in rodents (class warning); GI AEs in clinicConjunctivitis, injection-site reactions, eosinophilia; herpes zoster caution.GI events (nausea, diarrhea) most common; gallbladder disease; thyroid C-cell rodent findings.
Toxicology
CRS
N/AN/AN/A
Clinical
Safety signal
Thyroid C-cell tumors in rodents (class warning); GI AEs in clinicConjunctivitis, injection-site reactions, eosinophilia; herpes zoster caution.GI 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 NCT03480022ClinicalTrials.gov NCT02912468
Clinical
Program phase
APPROVEDAPPROVEDAPPROVED
Clinical
Trial activity
No active/completed countsNo active/completed countsNo active/completed counts
Clinical
Trial ref
NCT03480022NCT02912468
Preclinical
Animal (cat.)
MouseMouse