IP Library › Granted Patent US 12,016,932
Granted Patent B2
US 12,016,932 · App. 18/055,823 · Granted Jun 25, 2024

Gene editing for hemophilia A with improved factor VIII expression

Inventor: Alan Richard Brooks (Cambridge, MA)
Assignees: CRISPR THERAPEUTICS AG; BAYER HEALTHCARE LLC
A61K48/0058A61K48/0066A61K48/0075C12N15/113C12N2310/141
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,016,932
App. No.
18/055,823
Granted
Jun 25, 2024
Kind
B2
Abstract

Provided herein, in some embodiments, are materials and methods for treating hemophilia A in a subject ex vivo or in vivo. Also provided herein, in some embodiments, are materials and methods for knocking in a coding sequence encoding a synthetic FVIII having a B domain substitute into a genome.

Claims (13)

1. A nucleic acid, comprising a nucleotide sequence encoding a synthetic FVIII protein, wherein the synthetic FVIII protein comprises a B domain substitute, and wherein the B domain substitute comprises the amino acid sequence of any one of SEQ ID NOs: 362-364, 366-369, 371, and 373.

2. The nucleic acid of claim 1 , wherein the B domain substitute comprises the amino acid sequence of SEQ ID NO: 364.

3. The nucleic acid of claim 1 , wherein the nucleotide sequence encoding the synthetic FVIII protein is codon optimized for expression in a host cell.

4. The nucleic acid of claim 1 , wherein the nucleotide sequence encoding the synthetic FVIII protein comprises a reduced content of CpG di-nucleotides as compared to a wild-type nucleic acid sequence encoding FVIII.

5. The nucleic acid of claim 1 , wherein the nucleotide sequence encoding the synthetic FVIII does not comprise CpG di-nucleotides.

6. The nucleic acid of claim 1 , wherein the nucleic acid is a donor template.

7. The nucleic acid of claim 6 , wherein the donor template comprises a donor cassette comprising the nucleotide sequence encoding the synthetic FVIII protein, and wherein the donor cassette is flanked on one or both sides by a gRNA target site.

8. The nucleic acid of claim 1 , wherein the nucleic acid is located in a viral vector.

9. The nucleic acid of claim 8 , wherein the viral vector is an adeno-associated virus (AAV) vector.

10. A cell, wherein the genome of the cell comprises the nucleic acid of claim 1 .

11. The cell of claim 10 , wherein the nucleotide sequence encoding the synthetic FVIII protein is operably linked to an endogenous albumin promoter, an endogenous transferrin promoter, or an endogenous fibrinogen alpha promoter in the genome of the cell.

12. The cell of claim 10 , wherein the cell is a human liver cell, a human hepatocyte, or a human sinusoid epithelial cell.

13. A synthetic FVIII protein, wherein the synthetic FVIII protein comprises a B domain substitute, and wherein the B domain substitute comprises the amino acid sequence of any one of SEQ ID NOs: 362-364, 366-369, 371, and 373.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 17, 2022
From: BROOKS, ALAN RICHARD
To: CASEBIA THERAPEUTICS LIMITED LIABILITY PARTNERSHIP
Reel/Frame 061808/0929 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 17, 2022
From: BROOKS, ALAN RICHARD
To: CASEBIA THERAPEUTICS LIMITED LIABILITY PARTNERSHIP
Reel/Frame 061810/0468 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 17, 2022
From: CASEBIA THERAPEUTICS LIMITED LIABILITY PARTNERSHIP
To: CRISPR THERAPEUTICS AG; BAYER HEALTHCARE LLC
Reel/Frame 061810/0667 →
Continuity (4)
Continuation 16849796 · Apr 15, 2020
Provisional Application 62857782 · Jun 5, 2019
Provisional Application 62806702 · Feb 15, 2019
Related Publication 20230285597A1 · Sep 14, 2023