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항목
AntibodyCurated CoreFDAstaleApproved
adalimumab (Humira, Hyrimoz, Amjevita)
AbbVie·TNF-α
574 trials
AntibodyCurated CoreFDAstaleApproved
ustekinumab (Stelara, Wezlana)
Johnson & Johnson·IL-12 / IL-23 (p40)
195 trials
Overview
Program
Humira (adalimumab)Stelara (ustekinumab)
Overview
Company
AbbVieJohnson & Johnson
Overview
Modality
ANTIBODYANTIBODY
Overview
Target
TNF-αIL-12 / IL-23 (p40)
Overview
Indication
Rheumatoid arthritis, psoriasis, Crohn's disease, ulcerative colitis, axial SpAPsoriasis, psoriatic arthritis, Crohn's disease, ulcerative colitis
Overview
Phase
APPROVEDAPPROVED
Overview
Status
APPROVEDAPPROVED
Overview
Content status
Curated CoreCurated Core
Overview
Data Confidence
Editorial scope · Curated CoreEditorial scope · Curated Core
Overview
Development Signal
Development Signal · EstablishedDevelopment Signal · Established
Overview
Approval status
FDA approvedFDA approved
Positioning
Key differentiator
novel object recognition testNovel 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.IL-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).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).biomarkers but require external validation in independent cohorts
Toxicology
Species
Cynomolgus monkeyCynomolgus 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.Infections, reversible posterior leukoencephalopathy syndrome (rare), hypersensitivity.
Toxicology
CRS
N/AN/A
Clinical
Safety signal
Serious infections (TB reactivation, invasive fungal), malignancy risk signal, injection-site reactions, and rare demyelinating events.Infections, reversible posterior leukoencephalopathy syndrome (rare), hypersensitivity.
Clinical
Program phase
APPROVEDAPPROVED
Clinical
Trial activity
No active/completed countsNo active/completed counts