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프로그램 비교

검색으로 10,000+ 프로그램 중 최대 5개를 골라 PK/PD · 독성 · 임상을 나란히 비교합니다. · 다음 갱신 D-14 · 마지막 7월 13일

현재 선택: 5 · Data Tier에서 열림

프로그램 상세에서 관심 등록 후 2개 이상 모으면 여기서 한 번에 비교할 수 있습니다.

API CSV23행 · 5개 프로그램

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항목
AntibodyFDAApproved
adalimumab (Humira, Hyrimoz, Amjevita)
AbbVie·TNF-α
ORR 98.85%
AntibodyFDAApproved
secukinumab (Cosentyx)
Novartis·IL-17A
ORR 78.1%·t½ 31 h
AntibodyFDAApproved
etanercept (Enbrel, Erelzi)
Amgen / Pfizer·TNF
ORR 73.4%·t½ 30 h
AntibodyFDAApproved
ustekinumab (Stelara, Wezlana)
Janssen·IL-12 / IL-23 (p40)
ORR 75%·t½ 19 h
AntibodyFDAApproved
risankizumab (Skyrizi)
AbbVie·IL-23 (p19)
ORR 90%·t½ 28 h
Overview
Program
Humira (adalimumab)Cosentyx (secukinumab)Enbrel (etanercept)Stelara (ustekinumab)Skyrizi (risankizumab)
Overview
Company
AbbVieNovartisAmgen / PfizerJanssenAbbVie
Overview
Modality
ANTIBODYANTIBODYANTIBODYANTIBODYANTIBODY
Overview
Target
TNF-αIL-17ATNFIL-12 / IL-23 (p40)IL-23 (p19)
Overview
Indication
Rheumatoid arthritis, psoriasis, Crohn's disease, ulcerative colitis, axial SpAPsoriasis, psoriatic arthritis, ankylosing spondylitisRA, psoriasis, psoriatic arthritis, ankylosing spondylitisPsoriasis, psoriatic arthritis, Crohn's disease, ulcerative colitisPsoriasis, psoriatic arthritis, Crohn's disease
Overview
Phase
APPROVEDAPPROVEDAPPROVEDAPPROVEDAPPROVED
Overview
Status
APPROVEDAPPROVEDAPPROVEDAPPROVEDAPPROVED
MoA
Mechanism
Adalimumab products bind specifically to TNF-alpha and block its interaction with the p55 and p75 cell surface TNF receptorsTargeted immunotherapies provide effective interventions by disrupting these cytokine-driven pathwayDecoy receptor for TNF-α and lymphotoxintargeting IL-12 family signalingBlocks IL-23 p19 subunit
MoA
Biomarker
biomarkers to support personalized treatment strategiesbiomarkers and optimize therapeutic strategiesACR20, PASI75biomarkers but require external validation in independent cohortsPASI, sPGA
PK/PD
Half-life
31 h30 h19 h28 h
PK/PD
Species
Rat, xenografts, which corroboratRat, HumanRabbit, precluding FDA approval.Cynomolgus monkey, NHP, Marmoset, HumanMouse
PK/PD
Animal (cat.)
RatHuman, RatUnknownHuman, NHPMouse
PK/PD
Experiment
pharmacokineticpharmacokineticPDpharmacokineticpharmacokinetic
Toxicology
Species
Rat, xenografts, which corroboratMouse, Rat, HumanRabbit, precluding FDA approval.Cynomolgus monkey, NHP, Mouse, Marmoset, HumanCynomolgus monkey, Mouse
Toxicology
Animal (cat.)
UnknownMouseUnknownMouse, NHPNHP
Toxicology
Major finding
Interstitial lung disease, including pulmonary fibrosis, pulmonary embolism Skin reactions: Steveinterstitial lung disease Skin and subcutaneous tissue disorders: cutaneous lupus erythematosus,Hepatotoxicity: Drug-induced liver injury during induction treatment of inflammatory bowel
Clinical
Primary efficacy
ORR 98.85%ORR 78.1%ORR 73.4%ORR 75%ORR 90%
Clinical
PASI75
PASI 75 response rate at Week 12.67%PASI90 ~75% (ultIMMa-1) High skin clearance
Clinical
ORR
98.85%78.10%73.4%PASI75 ~67% (PsO pivotal)PASI90 ~75% (ultIMMa-1)
Clinical
Result source
ClinicalTrials.gov NCT00427921ClinicalTrials.gov NCT04732117ClinicalTrials.gov NCT01891864PHOENIXultIMMa
Clinical
Data Tier / Score
S · 92A · 91B · 91C · 91C · 91
Clinical
Program phase
APPROVEDAPPROVEDAPPROVEDAPPROVEDAPPROVED
Clinical
Clinical sync
2026년 7월 8일 (6일 전)2026년 7월 8일 (6일 전)2026년 7월 8일 (6일 전)2026년 7월 9일 (5일 전)2026년 7월 8일 (6일 전)