The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Aug. 09, 2022

Filed:

Jun. 10, 2016
Applicants:

The Broad Institute, Inc., Cambridge, MA (US);

Massachusetts Institute of Technology, Cambridge, MA (US);

Inventors:

Le Cong, Cambridge, MA (US);

David Benjamin Turitz Cox, Cambridge, MA (US);

Matthias Heidenreich, Boston, MA (US);

Randall Jeffrey Platt, Cambridge, MA (US);

Lukasz Swiech, Boston, MA (US);

Feng Zhang, Cambridge, MA (US);

Assignees:

THE BROAD INSTITUTE, INC., Cambridge, MA (US);

MASSACHUSETTS INSTITUTE OF TECHNOLOGY, Cambridge, MA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61K 48/00 (2006.01); C12N 9/22 (2006.01); C12N 15/90 (2006.01); C12N 15/10 (2006.01); A61K 9/00 (2006.01); A61K 38/46 (2006.01);
U.S. Cl.
CPC ...
C12N 9/22 (2013.01); A61K 9/0048 (2013.01); A61K 38/465 (2013.01); A61K 48/00 (2013.01); A61K 48/005 (2013.01); C12N 15/102 (2013.01); C12N 15/907 (2013.01); C12N 2750/14143 (2013.01);
Abstract

The invention provides for delivery, engineering and optimization of systems, methods, and compositions for manipulation of sequences and/or activities of target sequences. Provided are delivery systems and tissues or organ which are targeted as sites for delivery. Also provided are vectors and vector systems some of which encode one or more components of a CRISPR complex, as well as methods for the design and use of such vectors. Also provided are methods of directing CRISPR complex formation in eukaryotic cells to ensure enhanced specificity for target recognition and avoidance of toxicity and to edit or modify a target site in a genomic locus of interest to alter or improve the status of a disease or a condition.


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