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

현재 선택: 5 · Data Tier에서 열림

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API CSV31행 · 5개 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
AntibodyCurated CoreFDAApproved
risankizumab-rzaa (Skyrizi, BI 655066, risankizumab)
AbbVie·IL-23 p19
110 trials·t½ 28 h
Overview
Program
Humira (adalimumab)Enbrel (etanercept)Cosentyx (secukinumab)Stelara (ustekinumab)Skyrizi (risankizumab-rzaa)
Overview
Company
AbbVieAmgen / PfizerNovartisJohnson & JohnsonAbbVie
Overview
Modality
ANTIBODYANTIBODYANTIBODYANTIBODYANTIBODY
Overview
Target
TNF-αTNF (decoy receptor)IL-17AIL-12 / IL-23 (p40)IL-23 p19
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 colitisPlaque psoriasis, PsA, Crohn's disease, ulcerative colitis
Overview
Phase
APPROVEDAPPROVEDAPPROVEDAPPROVEDAPPROVED
Overview
Status
APPROVEDAPPROVEDAPPROVEDAPPROVEDAPPROVED
Overview
Content status
Curated CoreCurated CoreCurated CoreCurated CoreCurated Core
Overview
Data Confidence
Data Confidence · HighData Confidence · HighData Confidence · HighData Confidence · HighData Confidence · High
Overview
Development Signal
Development Signal · EstablishedDevelopment Signal · EstablishedDevelopment Signal · EstablishedDevelopment Signal · EstablishedDevelopment Signal · Established
Overview
Approval status
FDA approvedFDA 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 encouraNovel 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.IL-17 independent disease and immunogenicity.
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.Risankizumab selectively binds IL-23 p19 subunit, blocking IL-23 interaction with IL-23R and downstream Th17 pathway (IL-17A/F, IL-22).
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 cohortsPASI, sPGA, IBD endoscopic scores.
PK/PD
Half-life
~14–19 days (SC)30 h31 h19 h28 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 IBDMouse
PK/PD
Animal (cat.)
RatRat, In vitroHuman, MouseMouseMouse
PK/PD
Experiment
pdpharmacokineticPDPharmacokineticPharmacokinetic
Toxicology
Species
Cynomolgus monkey, Rat, xenografts, which corroboratRatMouse, HumanCynomolgus monkey, MouseCynomolgus 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.Upper respiratory infections, headache, fatigue; low TB reactivation vs TNF class.
Toxicology
CRS
N/AN/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.Upper respiratory infections, headache, fatigue; low TB reactivation vs TNF class.
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
APPROVEDAPPROVEDAPPROVEDAPPROVEDAPPROVED
Clinical
Trial activity
No active/completed countsNo active/completed countsNo active/completed countsNo active/completed countsNo active/completed counts
Clinical
Trial ref
NCT02405780NCT01891864NCT04300296PHOENIX
Preclinical
Animal (cat.)
RatMouse