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항목
AntibodyCurated CoreFDAApproved
secukinumab (Cosentyx, AIN457)
Novartis·IL-17A
229 trials·t½ 31 h
Overview
Program
Cosentyx (secukinumab)
Overview
Company
Novartis
Overview
Modality
ANTIBODY
Overview
Target
IL-17A
Overview
Indication
Psoriasis, PsA, AS, nr-axSpA, HS
Overview
Phase
APPROVED
Overview
Status
APPROVED
Overview
Content status
Curated Core
Overview
Data Confidence
Data Confidence · High
Overview
Development Signal
Development Signal · Established
Overview
Approval status
FDA approved
Positioning
Key differentiator
Novel approaches, including tolerogenic DC therapy and neuroimmune modulation, hold promise for refining treatment and addres
Positioning
Known limitation
bypassed its classic signal adaptor and directly interacted with the calcium-binding protein S100A9
MoA
Mechanism
Secukinumab binds IL-17A and prevents interaction with IL-17RA/RC receptor complex, inhibiting keratinocyte and synovial inflammation driven by Th17 pathway.
MoA
Biomarker
PASI, ASAS response, radiographic progression in SpA.
PK/PD
Half-life
31 h
PK/PD
Species
Mouse, Human, PASI75/90, IL-17A suppression
PK/PD
Animal (cat.)
Human, Mouse
PK/PD
Experiment
PD
Toxicology
Species
Mouse, Human
Toxicology
Major finding
Nasopharyngitis, candidiasis (mucocutaneous), neutropenia; IBD caution in label.
Toxicology
CRS
N/A
Clinical
Safety signal
Nasopharyngitis, candidiasis (mucocutaneous), neutropenia; IBD caution in label.
Clinical
Selected reported efficacy
44%
Clinical
Result source
ClinicalTrials.gov NCT04300296
Clinical
Program phase
APPROVED
Clinical
Trial activity
No active/completed counts
Clinical
Trial ref
NCT04300296