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현재 선택: 2 · 임상 갱신 필요 1 · Data Tier에서 열림

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항목
AntibodyCurated CoreFDAApproved
adalimumab (Humira, Hyrimoz, Amjevita)
AbbVie·TNF-α
574 trials·t½ ~14–19 days (SC)
AntibodyLimited DatastalePhase 3
Anti-TNF (Anti-TNF)
Abu Dhabi Stem Cells Center·Dementia
92 trials·t½ 248.54 days
Overview
Program
Humira (adalimumab)Anti-TNF
Overview
Company
AbbVieAbu Dhabi Stem Cells Center
Overview
Modality
ANTIBODYANTIBODY
Overview
Target
TNF-αDementia
Overview
Indication
Rheumatoid arthritis, psoriasis, Crohn's disease, ulcerative colitis, axial SpARheumatoid Arthritis
Overview
Phase
APPROVEDPHASE_3
Overview
Status
APPROVEDACTIVE
Overview
Content status
Curated CoreLimited Data
Overview
Data Confidence
Data Confidence · HighData Confidence · Low
Overview
Development Signal
Development Signal · EstablishedDevelopment Signal · Emerging
Overview
Approval status
FDA approvedInvestigational
Positioning
Key differentiator
novel object recognition test
Positioning
Known limitation
Anti-drug antibodies, TNF-independent inflammation, and immunogenicity lowering trough levels.
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).Targeting viral protein‑host signaling
MoA
Biomarker
CRP, ESR, disease-specific scores (DAS28, PASI, Mayo for IBD).biomarkers, microbiome profiling, and artificial intelligence in enabling adaptive and personalized asthma ma
PK/PD
Half-life
~14–19 days (SC)248.54 days
PK/PD
Species
Rat, xenografts, which corroborat, CRP reduction, clinical remission scoresMouse
PK/PD
Animal (cat.)
RatMouse
PK/PD
Experiment
pdpharmacokinetic
Toxicology
Species
Cynomolgus monkey, Rat, xenografts, which corroboratMouse
Toxicology
Animal (cat.)
NHPMouse
Toxicology
Major finding
Serious infections (TB reactivation, invasive fungal), malignancy risk signal, injection-site reactions, and rare demyelinating events.Decoding Biological Drug Names in Dermatology: The Post-2022 WHO Nomenclature Revision and Its Implications for Clinical Practice.. The WHO International Nonproprietary Names (INN) system for monoclonal antibodies underwent its most fundamental revision in 2021-2022, retiring the universal -mab suffix and replacing it with four structure-based stems (-tug, -bart, -ment, -mig). Simultaneously, new …
Toxicology
CRS
N/Agrade 3
Clinical
Safety signal
Serious infections (TB reactivation, invasive fungal), malignancy risk signal, injection-site reactions, and rare demyelinating events.Decoding Biological Drug Names in Dermatology: The Post-2022 WHO Nomenclature Revision and Its Implications for Clinical Practice.. The WHO International Nonproprietary Names (INN) system for monoclonal antibodies underwent its most fundamental revision in 2021-2022, retiring the universal -mab suffix and replacing it with four structure-based stems (-tug, -bart, -ment, -mig). Simultaneously, new …
Clinical
Result source
ClinicalTrials.gov NCT02405780
Clinical
Program phase
APPROVEDPHASE_3
Clinical
Trial activity
No active/completed countsNo active/completed counts
Clinical
Trial ref
NCT02405780