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프로그램 비교

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API CSV22행 · 2개 프로그램

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항목
AntibodyCurated CoreFDAstaleApproved
aflibercept (Eylea, VEGF Trap-Eye, Eylea HD, Zaltrap)
Regeneron / Bayer·VEGF-A / VEGF-B / PIGF
244 trials
AntibodyCurated CoreFDAstaleApproved
ranibizumab (Lucentis, Byooviz, Cimerli)
Roche / Genentech·VEGF-A
234 trials
Overview
Program
Eylea (aflibercept)Lucentis (ranibizumab)
Overview
Company
Regeneron / BayerRoche / Genentech
Overview
Modality
ANTIBODYANTIBODY
Overview
Target
VEGF-A / VEGF-B / PIGFVEGF-A
Overview
Indication
Wet AMD, DME, RVO, diabetic retinopathyWet AMD, DME, RVO, myopic CNV
Overview
Phase
APPROVEDAPPROVED
Overview
Status
APPROVEDAPPROVED
Overview
Content status
Curated CoreCurated Core
Overview
Data Confidence
Editorial scope · Curated CoreEditorial scope · Curated Core
Overview
Development Signal
Development Signal · EstablishedDevelopment Signal · Established
Overview
Approval status
FDA approvedFDA approved
Positioning
Key differentiator
unique recordsNovel metrics that included Visual Acuity Recovery Rate (VARR), Time to 1
Positioning
Known limitation
Tachyphylaxis, fibrosis, and need for shorter dosing intervals in subset of patients.Anatomic non-response and fibrotic disease; switch/combination with other anti-VEGF agents.
MoA
Mechanism
Aflibercept acts as a soluble decoy receptor binding VEGF-A, VEGF-B, and PlGF with higher affinity than native VEGFR, preventing activation of VEGFR1/2 and reducing pathological angiogenesis and vascular permeability in the retina.Ranibizumab is a humanized Fab fragment that binds all isoforms of VEGF-A, preventing VEGFR activation and reducing neovascularization and retinal edema.
MoA
Biomarker
biomarkers can reliably diagnose and monitor PCV, restricting the role of invasive indocyanine green angiograbiomarker of treatment response, supporting further validation in larger independent cohorts
Toxicology
Species
Cynomolgus monkey—
Toxicology
Animal (cat.)
NHP—
Toxicology
Major finding
Conjunctival hemorrhage, eye pain, cataract, vitreous detachment; endophthalmitis risk with injection procedure.Intraocular inflammation, retinal detachment, arterial thromboembolic events (low incidence).
Toxicology
CRS
N/AN/A
Clinical
Safety signal
Conjunctival hemorrhage, eye pain, cataract, vitreous detachment; endophthalmitis risk with injection procedure.Intraocular inflammation, retinal detachment, arterial thromboembolic events (low incidence).
Clinical
Program phase
APPROVEDAPPROVED
Clinical
Trial activity
No active/completed countsNo active/completed counts