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항목
AntibodyCurated CorestaleApproved
Certolizumab pegol (Certolizumab pegol)
Mario Negri Institute for Pharmaco…·Crohn's Disease
60 trials·t½ 14 h
Overview
Program
Certolizumab pegol
Overview
Company
Mario Negri Institute for Pharmacological Research
Overview
Modality
ANTIBODY
Overview
Target
Crohn's Disease
Overview
Indication
Rheumatoid Arthritis
Overview
Phase
APPROVED
Overview
Status
ACTIVE
Overview
Content status
Curated Core
Overview
Data Confidence
Data Confidence · High
Overview
Development Signal
Development Signal · Established
Overview
Approval status
Approved (flag incomplete)
Positioning
Key differentiator
Novelty assessment and Weibull modeling were applied to characterize signal strength and temporal risk patterns, acknowledgin
MoA
Mechanism
Targeted immunotherapies provide effective interventions by disrupting these cytokine-driven pathway
MoA
Biomarker
biomarkers (including sFlt-1/PlGF), standardized endpoints, and detailed safety follow-up are needed before a
PK/PD
Half-life
14 h
PK/PD
Species
Mouse
PK/PD
Animal (cat.)
Mouse
PK/PD
Experiment
Pharmacokinetic
Toxicology
Species
Mouse
Toxicology
Animal (cat.)
Mouse
Toxicology
Major finding
Pharmacokinetics of Certolizumab Pegol in Pregnancy: Results from the Open-Label CHERISH Study.. Control of chronic inflammatory diseases (CIDs) during pregnancy is essential for maternal and foetal health; however, the impact of pregnancy on the pharmacokinetics (PK) of CID therapies is unknown. This study investigated the impact of pregnancy on the PK of certolizumab pegol (CZP), a tumour necros…
Clinical
Safety signal
Pharmacokinetics of Certolizumab Pegol in Pregnancy: Results from the Open-Label CHERISH Study.. Control of chronic inflammatory diseases (CIDs) during pregnancy is essential for maternal and foetal health; however, the impact of pregnancy on the pharmacokinetics (PK) of CID therapies is unknown. This study investigated the impact of pregnancy on the PK of certolizumab pegol (CZP), a tumour necros…
Clinical
Result source
ClinicalTrials.gov NCT00845663
Clinical
Program phase
APPROVED
Clinical
Trial ref
NCT00845663