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항목
AntibodyCurated CoreFDAstaleApproved
dupilumab (Dupixent, REGN668)
Sanofi / Regeneron·IL-4Rα
278 trials
AntibodyLimited DatastaleApproved
Stopping dupilumab (Stopping dupilumab)
Sanofi / Regeneron·Severe Asthma
1 trials
Overview
Program
Dupixent (dupilumab)Stopping dupilumab
Overview
Company
Sanofi / RegeneronSanofi / Regeneron
Overview
Modality
ANTIBODYANTIBODY
Overview
Target
IL-4RαSevere Asthma
Overview
Indication
Atopic dermatitis, asthma, CRSwNP, EoE, prurigo nodularisSevere Asthma
Overview
Phase
APPROVEDAPPROVED
Overview
Status
APPROVEDRECRUITING
Overview
Content status
Curated CoreLimited Data
Overview
Data Confidence
Editorial scope · Curated CoreEditorial scope · limited data
Overview
Development Signal
Development Signal · EstablishedDevelopment Signal · Established
Overview
Approval status
FDA approvedApproved (flag incomplete)
Positioning
Key differentiator
Novel targets under investigation include MRGPRs, PARs, KIT receptors, OX-40, and sodium channels—
Positioning
Known limitation
Non-Type 2 inflammation and inadequate trough levels.—
MoA
Mechanism
Dupilumab binds IL-4Rα subunit shared by IL-4 type I and IL-13 type II receptors, inhibiting IL-4 and IL-13 signaling, reducing Type 2 inflammation (IgE, eosinophils, Th2 cytokines).—
MoA
Biomarker
biomarkers and clinical characteristics and highlight the need for standardized, methodologically rigorous fu—
Toxicology
Species
Mouse—
Toxicology
Major finding
Conjunctivitis, injection-site reactions, eosinophilia; herpes zoster caution.—
Toxicology
CRS
N/A—
Clinical
Safety signal
Conjunctivitis, injection-site reactions, eosinophilia; herpes zoster caution.—
Clinical
Program phase
APPROVEDAPPROVED
Clinical
Trial activity
No active/completed counts—