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

현재 선택: 4 · 임상 갱신 필요 2 · 차세대 보드에서 열림

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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
AntibodyLimited DatastalePhase 3
TNFi (TNFi, Tumor Necrosis Factor inhibitor, TNFi (Tumor Necrosis Factor inhibitor) medication)
Bristol-Myers Squibb·Polyarticular Course Juvenile Idio…
134 trials
AntibodyLimited DatastalePhase 3
Anti-TNF (Anti-TNF)
Abu Dhabi Stem Cells Center·Dementia
92 trials·t½ 248.54 days
Overview
Program
Humira (adalimumab)Enbrel (etanercept)TNFi (Tumor Necrosis Factor inhibitor) medicationAnti-TNF
Overview
Company
AbbVieAmgen / PfizerBristol-Myers SquibbAbu Dhabi Stem Cells Center
Overview
Modality
ANTIBODYANTIBODYANTIBODYANTIBODY
Overview
Target
TNF-αTNF (decoy receptor)Polyarticular Course Juvenile IdiopathicDementia
Overview
Indication
Rheumatoid arthritis, psoriasis, Crohn's disease, ulcerative colitis, axial SpARA, PsA, AS, plaque psoriasis, JIAPolyarticular Course Juvenile Idiopathic Arthritis (JIA)Rheumatoid Arthritis
Overview
Phase
APPROVEDAPPROVEDPHASE_3PHASE_3
Overview
Status
APPROVEDAPPROVEDRECRUITINGACTIVE
Overview
Content status
Curated CoreCurated CoreLimited DataLimited Data
Overview
Data Confidence
Data Confidence · HighData Confidence · HighData Confidence · LowData Confidence · Low
Overview
Development Signal
Development Signal · EstablishedDevelopment Signal · EstablishedDevelopment Signal · EmergingDevelopment Signal · Emerging
Overview
Approval status
FDA approvedFDA approvedInvestigationalInvestigational
Positioning
Key differentiator
novel object recognition testnovel ADAM17 inhibitor drugs to block soluble TNF-α production in inflammatory diseases
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.
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.Targeting specific cytokine pathwayTargeting viral protein‑host signaling
MoA
Biomarker
CRP, ESR, disease-specific scores (DAS28, PASI, Mayo for IBD).DAS28, PASI, CRP.biomarker for the effectiveness of mainly abatacept and other biologic disease-modifying antirheumatic drugsbiomarkers, microbiome profiling, and artificial intelligence in enabling adaptive and personalized asthma ma
PK/PD
Half-life
~14–19 days (SC)30 h248.54 days
PK/PD
Species
Rat, xenografts, which corroborat, CRP reduction, clinical remission scoresRat, CRP, joint counts, skin scoresMouse, Rat, HumanMouse
PK/PD
Animal (cat.)
RatRat, In vitroHuman, Mouse, Rat, In vitroMouse
PK/PD
Experiment
pdpharmacokineticpdpharmacokinetic
Toxicology
Species
Cynomolgus monkey, Rat, xenografts, which corroboratRatMouse, Rat, HumanMouse
Toxicology
Animal (cat.)
NHPHuman, Mouse, Rat, In vitroMouse
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.Whole-blood coagulation and platelet dynamics identify differential prothrombotic states in patients with rheumatoid arthritis treated with JAK or TNF-ɑ inhibitors.. Rheumatoid arthritis (RA) is associated with inflammation-driven hypercoagulability and increased venous thromboembolic risk. Post hoc analyses of safety trials have raised concerns regarding a potential differential thrombotic …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/AN/Agrade 3
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.Whole-blood coagulation and platelet dynamics identify differential prothrombotic states in patients with rheumatoid arthritis treated with JAK or TNF-ɑ inhibitors.. Rheumatoid arthritis (RA) is associated with inflammation-driven hypercoagulability and increased venous thromboembolic risk. Post hoc analyses of safety trials have raised concerns regarding a potential differential thrombotic …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
Selected reported efficacy
73.4%27.5%
Clinical
PASI75
PASI 75 response rate at Week 12.
Clinical
Result source
ClinicalTrials.gov NCT02405780ClinicalTrials.gov NCT01891864ClinicalTrials.gov NCT02015520
Clinical
Program phase
APPROVEDAPPROVEDPHASE_3PHASE_3
Clinical
Trial activity
No active/completed countsNo active/completed countsNo active/completed countsNo active/completed counts
Clinical
Trial ref
NCT02405780NCT01891864NCT02015520
Preclinical
Animal (cat.)
Rat