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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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항목
AntibodyCurated CoreFDAApproved
dupilumab (Dupixent, REGN668)
Sanofi / Regeneron·IL-4Rα
278 trials·t½ ~14 days (300 mg q2w)
AntibodyCurated CoreFDAApproved
lebrikizumab-lbkz (Ebglyss, LY3650150, lebrikizumab)
Eli Lilly·IL-13
108 trials·t½ 24.5 h
Overview
Program
Dupixent (dupilumab)Ebglyss (lebrikizumab-lbkz)
Overview
Company
Sanofi / RegeneronEli Lilly
Overview
Modality
ANTIBODYANTIBODY
Overview
Target
IL-4RαIL-13
Overview
Indication
Atopic dermatitis, asthma, CRSwNP, EoE, prurigo nodularisModerate-to-severe atopic dermatitis
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
Novel targets under investigation include MRGPRs, PARs, KIT receptors, OX-40, and sodium channelsunique disposition of simvastatin rather than enzyme or transporter inhibition
Positioning
Known limitation
Non-Type 2 inflammation and inadequate trough levels.Concurrent IL-4 signaling and non-Type 2 dermatitis.
MoA
Mechanism
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).Lebrikizumab binds IL-13 with high affinity, blocking IL-13Rα1/IL-4Rα signaling and downstream Type 2 inflammation in skin (barrier dysfunction, pruritus, eosinophilia).
MoA
Biomarker
biomarkers and clinical characteristics and highlight the need for standardized, methodologically rigorous fuEASI, IGA 0/1, pruritus NRS.
PK/PD
Half-life
~14 days (300 mg q2w)24.5 h
PK/PD
Species
Mouse, EASI-75, peak pruritus NRS reductionNHP
PK/PD
Animal (cat.)
MouseNHP
PK/PD
Experiment
PDpd
Toxicology
Species
MouseCynomolgus monkey, NHP
Toxicology
Major finding
Conjunctivitis, injection-site reactions, eosinophilia; herpes zoster caution.Conjunctivitis, nasopharyngitis, injection-site reactions; herpes zoster warnings per class.
Toxicology
CRS
N/AN/A
Clinical
Safety signal
Conjunctivitis, injection-site reactions, eosinophilia; herpes zoster caution.Conjunctivitis, nasopharyngitis, injection-site reactions; herpes zoster warnings per class.
Clinical
Selected reported efficacy
1%
Clinical
Result source
ClinicalTrials.gov NCT02912468ClinicalTrials.gov NCT03689855
Clinical
Program phase
APPROVEDAPPROVED
Clinical
Trial activity
No active/completed countsNo active/completed counts
Clinical
Trial ref
NCT02912468NCT03689855
Preclinical
Animal (cat.)
Mouse