← 홈

프로그램 비교

타깃 · 모달리티 · 임상 근거 · 비임상 맥락으로 최대 5개 프로그램을 나란히 비교합니다. · 다음 갱신 D-6 · 마지막 9월 2일

현재 선택: 3

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

API CSV31행 · 3개 프로그램

표가 넓으면 좌우로 스크롤하세요. 핵심 비교 모드에서는 중요 항목만 표시됩니다.

항목
AntibodyCurated CoreFDAApproved
guselkumab (Tremfya, CNTO 1959)
Johnson & Johnson·IL-23 p19
87 trials·t½ ~15–18 days
AntibodyCurated CoreFDAApproved
risankizumab-rzaa (Skyrizi, BI 655066, risankizumab)
AbbVie·IL-23 p19
110 trials·t½ 28 h
AntibodyCurated CoreFDAApproved
ustekinumab (Stelara, Wezlana)
Johnson & Johnson·IL-12 / IL-23 (p40)
195 trials·t½ 19 h
Overview
Program
Tremfya (guselkumab)Skyrizi (risankizumab-rzaa)Stelara (ustekinumab)
Overview
Company
Johnson & JohnsonAbbVieJohnson & Johnson
Overview
Modality
ANTIBODYANTIBODYANTIBODY
Overview
Target
IL-23 p19IL-23 p19IL-12 / IL-23 (p40)
Overview
Indication
Plaque psoriasis, psoriatic arthritis, ulcerative colitis, Crohn's diseasePlaque psoriasis, PsA, Crohn's disease, ulcerative colitisPsoriasis, psoriatic arthritis, Crohn's disease, ulcerative colitis
Overview
Phase
APPROVEDAPPROVEDAPPROVED
Overview
Status
APPROVEDAPPROVEDAPPROVED
Overview
Content status
Curated CoreCurated CoreCurated Core
Overview
Data Confidence
Data Confidence · HighData Confidence · HighData Confidence · High
Overview
Development Signal
Development Signal · EstablishedDevelopment Signal · EstablishedDevelopment Signal · Established
Overview
Approval status
FDA approvedFDA approvedFDA approved
Positioning
Key differentiator
Leaving IL-12 intact preserves Th1 antimicrobial immunity while shutting down the Th17 axis, which is why durability is high and infection signals are low.Novel therapeutic avenues, including TYK2 and HDAC inhibitors, as well as nanotechnology-based delivery systems, show encouraNovel therapeutic avenues, including TYK2 and HDAC inhibitors, as well as nanotechnology-based delivery systems, show encoura
Positioning
Known limitation
Anti-drug antibodies are rare; non-IL-23-driven fibrostenotic disease does not respond.IL-17 independent disease and immunogenicity.IL-23 axis escape, anti-drug antibodies, and non-IL-12/23 inflammation.
Positioning
Development positioning
IL-23 class benchmark alongside Skyrizi, now with the broadest IBD label progression.
MoA
Mechanism
Neutralizes IL-23 by binding p19, blocking IL-23R signaling and downstream Th17/Th22 differentiation, IL-17 production, and tissue inflammation in skin, joints, and gut mucosa.Risankizumab selectively binds IL-23 p19 subunit, blocking IL-23 interaction with IL-23R and downstream Th17 pathway (IL-17A/F, IL-22).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
PASI/IGA in psoriasis, ACR20 in PsA, endoscopic improvement and fecal calprotectin in IBD.PASI, sPGA, IBD endoscopic scores.biomarkers but require external validation in independent cohorts
PK/PD
Half-life
~15–18 days28 h19 h
PK/PD
Species
Cynomolgus monkey, PASI 90/100, ACR20/50, endoscopic remission, serum IL-17A/IL-22MouseMouse, Skin clearance (PASI75/90), endoscopic response in IBD
PK/PD
Animal (cat.)
Human, NHPMouseMouse
PK/PD
Experiment
PharmacokineticPharmacokineticPharmacokinetic
Toxicology
Species
Mouse, PigCynomolgus monkey, MouseCynomolgus monkey, Mouse
Toxicology
Major finding
Upper respiratory infection, headache, and injection-site reactions dominate. Serious infection and malignancy signals have stayed low across long-term psoriasis follow-up.Upper respiratory infections, headache, fatigue; low TB reactivation vs TNF class.Infections, reversible posterior leukoencephalopathy syndrome (rare), hypersensitivity.
Toxicology
CRS
N/AN/AN/A
Clinical
Safety signal
Upper respiratory infection, headache, and injection-site reactions dominate. Serious infection and malignancy signals have stayed low across long-term psoriasis follow-up.Upper respiratory infections, headache, fatigue; low TB reactivation vs TNF class.Infections, reversible posterior leukoencephalopathy syndrome (rare), hypersensitivity.
Clinical
Selected reported efficacy
PASI75 67%
Clinical
PASI75
67%
Clinical
Result source
PHOENIX
Clinical
Program phase
APPROVEDAPPROVEDAPPROVED
Clinical
Trial activity
No active/completed countsNo active/completed countsNo active/completed counts
Clinical
Trial ref
PHOENIX
Preclinical
Animal (cat.)
MouseMouse