Oxidation-resistant AAT gene therapy
US12031144B2 · kind B2 · utility
0Cited by
5References
19Claims
0Family size
Assignee
Inventors
Key dates
| Filing date | Mar 29, 2018 |
| Grant date | Jul 9, 2024 |
| Priority date | — |
| Expiry date | Dec 26, 2039 |
Classification
- Technology area (CPC C)Chemistry; Metallurgy
- CPC primaryC12N2750/14144
- WIPO fieldPharmaceuticals
- WIPO sectorChemistry
Abstract
A gene therapy treatment for alpha 1-antitrypsin (AAT) deficiency is provided comprising a plasmid or viral, e.g., an AAV, vector coding for an elastase- or cathepsin G-inhibiting, oxidation-resistant human AAT with a substitution at, for example, Met358 and/or Met351.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.