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프로그램 비교

검색으로 10,000+ 프로그램 중 최대 5개를 골라 PK/PD · 독성 · 임상을 나란히 비교합니다. · 다음 갱신 D-8 · 마지막 7월 21일

현재 선택: 4 · 임상 갱신 필요 3 · Data Tier에서 열림

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

API CSV22행 · 4개 프로그램

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항목
AntibodyFDAApproved
adalimumab (Humira, Hyrimoz, Amjevita)
AbbVie·TNF-α
ORR 98.85%
AntibodystaleApproved
rituximab (Rituxan)
Roche / Genentech·Pompe Disease
ORR 83%
AntibodystaleApproved
Mabthera (Mabthera)
Roche / Genentech·FRα
ORR 84.7%
AntibodystaleApproved
Abatacept (Abatacept)
Novartis Pharmaceuticals·Rheumatoid Arthritis
ORR 6.35%·t½ 14.3 h
Overview
Program
Humira (adalimumab)RituxanMabtheraAbatacept
Overview
Company
AbbVieRoche / GenentechRoche / GenentechNovartis Pharmaceuticals
Overview
Modality
ANTIBODYANTIBODYANTIBODYANTIBODY
Overview
Target
TNF-αPompe DiseaseFRαRheumatoid Arthritis
Overview
Indication
Rheumatoid arthritis, psoriasis, Crohn's disease, ulcerative colitis, axial SpARheumatoid ArthritisRheumatoid ArthritisRheumatoid Arthritis
Overview
Phase
APPROVEDAPPROVEDAPPROVEDAPPROVED
Overview
Status
APPROVEDACTIVEACTIVEACTIVE
MoA
Mechanism
Adalimumab products bind specifically to TNF-alpha and block its interaction with the p55 and p75 cell surface TNF receptorsCAR-T therapy induced profound, durable responses in extremely severe patients with seropositive PIRR
MoA
Biomarker
biomarkers to support personalized treatment strategiesCD20 mAbs: rituximab; ofatumumab; and obinutuzumab, were screened in highCD20-positive, lowbiomarker-derived score, to capture and predict the course of active lupus nephritis (LN) in adult patients
PK/PD
Half-life
14.3 h
PK/PD
Species
Rat, xenografts, which corroboratRabbitMouse, HumanMouse, Human
PK/PD
Animal (cat.)
RatIn vitroHuman, MouseHuman, Mouse, In vitro
PK/PD
Experiment
pharmacokineticpharmacokineticpharmacodynamicpd
Toxicology
Species
Rat, xenografts, which corroboratRabbitMouse, HumanCynomolgus monkey, Mouse, Rat, Hamster, Human
Toxicology
Animal (cat.)
UnknownIn vitroHuman, MouseMouse, Rat, NHP
Toxicology
Major finding
Interstitial lung disease, including pulmonary fibrosis, pulmonary embolism Skin reactions: Stevethrombocytopenia (p<0Thrombocytopenia in TP53-Aberrant Chronic Lymphocytic Leukemia: A Multimechanistic Case with Res
Clinical
Primary efficacy
ORR 98.85%ORR 83%ORR 84.7%ORR 6.35%
Clinical
ORR
98.85%83%84.7%6.35%
Clinical
Result source
ClinicalTrials.gov NCT00427921ClinicalTrials.gov NCT04665765ClinicalTrials.gov NCT02268045ClinicalTrials.gov NCT00124982
Clinical
Data Tier / Score
S · 92B · 67C · 65C · 41
Clinical
Program phase
APPROVEDAPPROVEDAPPROVEDAPPROVED
Clinical
Clinical sync
2026년 7월 18일 (8일 전)2026년 7월 9일 (18일 전 · 갱신 권장)2026년 7월 9일 (18일 전 · 갱신 권장)2026년 7월 8일 (19일 전 · 갱신 권장)