EP Patent

EP2924127A1 — Method and kit for prognosis of OPA1 gene induced diseases, e.g. Kjers optic atrophy.

Assigned to Centre National de la Recherche Scientifique CNRS · Expires 2015-09-30 · 11y expired

What this patent protects

The present invention provides the use of Nuclear factor (erythroid-derived 2)-like 2 (NRF2)-activated genes products, e.g. SOD1. CAT and ACO2 in the prognosis of an OPA1 gene- or OPA1 gene product- deficit-induced disease, or related complications, e.g. optic atrophy and optic n…

USPTO Abstract

The present invention provides the use of Nuclear factor (erythroid-derived 2)-like 2 (NRF2)-activated genes products, e.g. SOD1. CAT and ACO2 in the prognosis of an OPA1 gene- or OPA1 gene product- deficit-induced disease, or related complications, e.g. optic atrophy and optic neuropathy, in a biological sample selected from fibroblasts, epithelial cells, blood samples or a mixture thereof, of a patient affected or suspected to be affected by said disease.

Drugs covered by this patent

Patent Metadata

Patent number
EP2924127A1
Jurisdiction
EP
Classification
Expires
2015-09-30
Drug substance claim
No
Drug product claim
No
Assignee
Centre National de la Recherche Scientifique CNRS
Source
FDA Orange Book + USPTO grounding via Google Patents

Bibliographic data sourced from FDA Orange Book + USPTO public records. Plain-English summary generated by AI grounded in source text. Patent term extensions (PTR, SPC, pediatric) may shift the effective expiry. Not legal advice.

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