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타깃 · 모달리티 · 임상 근거 · 비임상 맥락으로 최대 5개 프로그램을 나란히 비교합니다. · 다음 갱신 D-6 · 마지막 9월 2일

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항목
CGTCurated CoreFDAApproved
voretigene neparvovec (Luxturna, AAV2-hRPE65v2, voretigene neparvovec-rzyl)
Spark Therapeutics / Roche·RPE65 (AAV2)
7 trials
Overview
Program
Luxturna (voretigene neparvovec)
Overview
Company
Spark Therapeutics / Roche
Overview
Modality
CGT
Overview
Target
RPE65 (AAV2)
Overview
Indication
Inherited retinal dystrophy due to confirmed biallelic RPE65 mutations
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
Surgical subretinal delivery; landmark ophthalmology gene therapy
Positioning
Known limitation
bypasses defective phototransduction pathways, showing promise for patients regardless of their genetic profile
Positioning
Development positioning
Only approved RPE65 gene therapy
Technology
Vector
AAV2
MoA
Mechanism
Voretigene neparvovec uses AAV2 to deliver functional RPE65 to retinal pigment epithelium, restoring the visual cycle and improving light sensitivity in RPE65-mutant IRD.
MoA
Biomarker
MLMT, FST, BCVA.
PK/PD
Species
NHP, Despite these findings, and no systemic toxicity was identified.
PK/PD
Animal (cat.)
NHP
PK/PD
Experiment
biodistribution
Toxicology
Species
NHP, Dog, Despite these findings, and no systemic toxicity was identified.
Toxicology
Animal (cat.)
NHP, Dog
Toxicology
Major finding
Procedure-related ocular AEs; inflammation manageable with steroids
Clinical
Safety signal
Procedure-related ocular AEs; inflammation manageable with steroids
Clinical
Program phase
APPROVED
Clinical
Trial activity
4 recruiting · 3 completed
Preclinical
Animal (cat.)
NHP