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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
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
AntibodyApproved
Remicade® (Remicade®)
Janssen·Ankylosing Spondylitis
ORR 56.6%
AntibodyPhase 2
Thiotepa (Thiotepa)
Paul Szabolcs·Leukemia, Acute
ORR 68%
Overview
Program
Humira (adalimumab)Stelara (ustekinumab)Skyrizi (risankizumab)Remicade®Thiotepa
Overview
Company
AbbVieJanssenAbbVieJanssenPaul Szabolcs
Overview
Modality
ANTIBODYANTIBODYANTIBODYANTIBODYANTIBODY
Overview
Target
TNF-αIL-12 / IL-23 (p40)IL-23 (p19)Ankylosing SpondylitisLeukemia, Acute
Overview
Indication
Rheumatoid arthritis, psoriasis, Crohn's disease, ulcerative colitis, axial SpAPsoriasis, psoriatic arthritis, Crohn's disease, ulcerative colitisPsoriasis, psoriatic arthritis, Crohn's diseaseCrohn's DiseaseCrohn's Disease
Overview
Phase
APPROVEDAPPROVEDAPPROVEDAPPROVEDPHASE_2
Overview
Status
APPROVEDAPPROVEDAPPROVEDACTIVEACTIVE
MoA
Mechanism
Adalimumab products bind specifically to TNF-alpha and block its interaction with the p55 and p75 cell surface TNF receptorstargeting IL-12 family signalingBlocks IL-23 p19 subunittargeted metabolomics, to delineate microbial and metabolic signatures predictive of IFX induction efficacy and to explore mechanistic pathway
MoA
Biomarker
biomarkers to support personalized treatment strategiesbiomarkers but require external validation in independent cohortsPASI, sPGAbiomarkers and safety profile were noted before and after switchbiomarkers that refine risk assessment
PK/PD
Half-life
19 h28 h
PK/PD
Species
Rat, xenografts, which corroboratCynomolgus monkey, NHP, Marmoset, HumanMouseMouse, HumanMouse, Rabbit
PK/PD
Animal (cat.)
RatHuman, NHPMouseHuman, MouseMouse
PK/PD
Experiment
pharmacokineticpharmacokineticpharmacokineticpharmacokineticpharmacokinetic
Toxicology
Species
Rat, xenografts, which corroboratCynomolgus monkey, NHP, Mouse, Marmoset, HumanCynomolgus monkey, MouseMouse, HumanMouse, Rat, Rabbit
Toxicology
Animal (cat.)
UnknownMouse, NHPNHPHuman, MouseMouse, Rat
Toxicology
Major finding
Interstitial lung disease, including pulmonary fibrosis, pulmonary embolism Skin reactions: SteveHepatotoxicity: Drug-induced liver injury during induction treatment of inflammatory bowelMultiple switches between infliximab originator and biosimilars in pediatric inflammatory bowel disease.. Infliximab (IFX) is highly effective but costly, driving the adoption of biosimilars. Data on switching from originator IFX to biosimilars in pediatric inflammatory bowel disease (IBD) patients remain limited. This study evaluated the safety and efficacy of switching from originator IFX to IFX…
Clinical
Primary efficacy
ORR 98.85%ORR 75%ORR 90%ORR 56.6%ORR 68%
Clinical
PASI75
67%PASI90 ~75% (ultIMMa-1) High skin clearance
Clinical
ORR
98.85%PASI75 ~67% (PsO pivotal)PASI90 ~75% (ultIMMa-1)17.2%68%
Clinical
Result source
ClinicalTrials.gov NCT00427921PHOENIXultIMMaClinicalTrials.gov NCT02990806ClinicalTrials.gov NCT00554788
Clinical
Data Tier / Score
S · 92A · 91B · 91C · 58C · 55
Clinical
Program phase
APPROVEDAPPROVEDAPPROVEDAPPROVEDPHASE_2
Clinical
Clinical sync
2026년 7월 8일 (6일 전)2026년 7월 9일 (5일 전)2026년 7월 8일 (6일 전)2026년 7월 9일 (5일 전)2026년 7월 9일 (5일 전)