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항목
AntibodyLimited DatastalePhase 3
CDP870 (Certolizumab Pegol, Certolizumab Pegol (CDP870))
UCB Pharma·Crohn's Disease
57 trials·t½ 14 h
Overview
Program
Certolizumab Pegol (CDP870)
Overview
Company
UCB Pharma
Overview
Modality
ANTIBODY
Overview
Target
Crohn's Disease
Overview
Indication
Crohn's Disease
Overview
Phase
PHASE_3
Overview
Status
ACTIVE
Overview
Content status
Limited Data
Overview
Data Confidence
Data Confidence · Low
Overview
Development Signal
Development Signal · Emerging
Overview
Approval status
Investigational
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, effectiveness and safety of certolizumab pegol in children and adolescents with active juvenile idiopathic arthritis: 9+-year results from a multicenter, open-label study.. To assess the pharmacokinetics, effectiveness, safety, and immunogenicity of certolizumab pegol (CZP) in polyarticular-course juvenile idiopathic arthritis (pcJIA). Pediatric Arthritis Study of Certolizumab Pe…
Clinical
Safety signal
Pharmacokinetics, effectiveness and safety of certolizumab pegol in children and adolescents with active juvenile idiopathic arthritis: 9+-year results from a multicenter, open-label study.. To assess the pharmacokinetics, effectiveness, safety, and immunogenicity of certolizumab pegol (CZP) in polyarticular-course juvenile idiopathic arthritis (pcJIA). Pediatric Arthritis Study of Certolizumab Pe…
Clinical
Selected reported efficacy
0.2%
Clinical
Result source
ClinicalTrials.gov NCT01235598
Clinical
Program phase
PHASE_3
Clinical
Trial ref
NCT01235598