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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 CSV31행 · 4개 프로그램

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항목
AntibodyCurated CoreFDAApproved
adalimumab (Humira, Hyrimoz, Amjevita)
AbbVie·TNF-α
574 trials·t½ ~14–19 days (SC)
AntibodyCurated CoreFDAApproved
etanercept (Enbrel, TNFR-Fc)
Amgen / Pfizer·TNF (decoy receptor)
236 trials·t½ 30 h
AntibodyCurated CoreFDAApproved
secukinumab (Cosentyx, AIN457)
Novartis·IL-17A
229 trials·t½ 31 h
AntibodyCurated CoreFDAApproved
ustekinumab (Stelara, Wezlana)
Johnson & Johnson·IL-12 / IL-23 (p40)
195 trials·t½ 19 h
Overview
Program
Humira (adalimumab)Enbrel (etanercept)Cosentyx (secukinumab)Stelara (ustekinumab)
Overview
Company
AbbVieAmgen / PfizerNovartisJohnson & Johnson
Overview
Modality
ANTIBODYANTIBODYANTIBODYANTIBODY
Overview
Target
TNF-αTNF (decoy receptor)IL-17AIL-12 / IL-23 (p40)
Overview
Indication
Rheumatoid arthritis, psoriasis, Crohn's disease, ulcerative colitis, axial SpARA, PsA, AS, plaque psoriasis, JIAPsoriasis, PsA, AS, nr-axSpA, HSPsoriasis, psoriatic arthritis, Crohn's disease, ulcerative colitis
Overview
Phase
APPROVEDAPPROVEDAPPROVEDAPPROVED
Overview
Status
APPROVEDAPPROVEDAPPROVEDAPPROVED
Overview
Content status
Curated CoreCurated CoreCurated CoreCurated Core
Overview
Data Confidence
Data Confidence · HighData Confidence · HighData Confidence · HighData Confidence · High
Overview
Development Signal
Development Signal · EstablishedDevelopment Signal · EstablishedDevelopment Signal · EstablishedDevelopment Signal · Established
Overview
Approval status
FDA approvedFDA approvedFDA approvedFDA approved
Positioning
Key differentiator
novel object recognition testnovel ADAM17 inhibitor drugs to block soluble TNF-α production in inflammatory diseasesNovel approaches, including tolerogenic DC therapy and neuroimmune modulation, hold promise for refining treatment and addresNovel therapeutic avenues, including TYK2 and HDAC inhibitors, as well as nanotechnology-based delivery systems, show encoura
Positioning
Known limitation
Anti-drug antibodies, TNF-independent inflammation, and immunogenicity lowering trough levels.Anti-drug antibodies (lower vs mAb TNF inhibitors), non-TNF pathways.bypassed its classic signal adaptor and directly interacted with the calcium-binding protein S100A9IL-23 axis escape, anti-drug antibodies, and non-IL-12/23 inflammation.
MoA
Mechanism
Adalimumab binds specifically to TNF-α and blocks its interaction with p55 and p75 cell-surface TNF receptors, neutralizing TNF-mediated inflammatory cascades (IL-6, adhesion molecules, acute-phase proteins).Etanercept is a dimeric fusion protein of human p75 TNF receptor linked to IgG1 Fc; it binds TNF-α and lymphotoxin-α, preventing receptor activation and downstream NF-κB inflammatory signaling.Secukinumab binds IL-17A and prevents interaction with IL-17RA/RC receptor complex, inhibiting keratinocyte and synovial inflammation driven by Th17 pathway.Ustekinumab binds the p40 subunit shared by IL-12 and IL-23, preventing their interaction with IL-12Rβ1 receptor and downstream Th1/Th17 differentiation and cytokine production.
MoA
Biomarker
CRP, ESR, disease-specific scores (DAS28, PASI, Mayo for IBD).DAS28, PASI, CRP.PASI, ASAS response, radiographic progression in SpA.biomarkers but require external validation in independent cohorts
PK/PD
Half-life
~14–19 days (SC)30 h31 h19 h
PK/PD
Species
Rat, xenografts, which corroborat, CRP reduction, clinical remission scoresRat, CRP, joint counts, skin scoresMouse, Human, PASI75/90, IL-17A suppressionMouse, Skin clearance (PASI75/90), endoscopic response in IBD
PK/PD
Animal (cat.)
RatRat, In vitroHuman, MouseMouse
PK/PD
Experiment
pdpharmacokineticPDPharmacokinetic
Toxicology
Species
Cynomolgus monkey, Rat, xenografts, which corroboratRatMouse, HumanCynomolgus monkey, Mouse
Toxicology
Animal (cat.)
NHP
Toxicology
Major finding
Serious infections (TB reactivation, invasive fungal), malignancy risk signal, injection-site reactions, and rare demyelinating events.Injection-site reactions, infections, rare demyelination and lupus-like syndrome.Nasopharyngitis, candidiasis (mucocutaneous), neutropenia; IBD caution in label.Infections, reversible posterior leukoencephalopathy syndrome (rare), hypersensitivity.
Toxicology
CRS
N/AN/AN/AN/A
Clinical
Safety signal
Serious infections (TB reactivation, invasive fungal), malignancy risk signal, injection-site reactions, and rare demyelinating events.Injection-site reactions, infections, rare demyelination and lupus-like syndrome.Nasopharyngitis, candidiasis (mucocutaneous), neutropenia; IBD caution in label.Infections, reversible posterior leukoencephalopathy syndrome (rare), hypersensitivity.
Clinical
Selected reported efficacy
73.4%44%PASI75 67%
Clinical
PASI75
PASI 75 response rate at Week 12.67%
Clinical
Result source
ClinicalTrials.gov NCT02405780ClinicalTrials.gov NCT01891864ClinicalTrials.gov NCT04300296PHOENIX
Clinical
Program phase
APPROVEDAPPROVEDAPPROVEDAPPROVED
Clinical
Trial activity
No active/completed countsNo active/completed countsNo active/completed countsNo active/completed counts
Clinical
Trial ref
NCT02405780NCT01891864NCT04300296PHOENIX
Preclinical
Animal (cat.)
Rat