IP Library Granted Patent US 10,507,249
Granted Patent B2
US 10,507,249 · App. 16/502,672 · Granted Dec 17, 2019

Lipid nanoparticle compositions and methods for mRNA delivery

Inventors: Braydon Charles Guild (Lexington, MA); Frank DeRosa (Lexington, MA); Michael Heartlein (Lexington, MA)
Assignee: Translate Bio, Inc.
A61K48/0008A61K9/0019A61K9/0073A61K9/1271A61K9/1272A61K9/5123A61K31/713A61K38/1816A61K38/47A61K38/4846A61K38/57A61K48/0075A61K48/0091C07K14/505C07K14/8125C12N9/2465C12N9/644C12N15/52C12N15/85C12Y302/01022C12Y304/21022A61K48/00
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Quick Facts
Patent No.
US 10,507,249
App. No.
16/502,672
Granted
Dec 17, 2019
Kind
B2
Abstract

Disclosed herein are compositions and methods for modulating the production of a protein in a target cell. The compositions and methods disclosed herein are capable of ameliorating diseases associated with protein or enzyme deficiencies.

Claims (22)

1. A method for pulmonary delivery of messenger RNA (mRNA) for in vivo production of a protein in the lung comprising administering via inhalation from a nebulizer to the lung of a subject, a composition comprising an mRNA that encodes the protein,

wherein the mRNA is encapsulated within a lipid nanoparticle comprising one or more PEG-modified lipids, and

wherein the administering of the composition results in detectable levels of the protein at least 72 hours after administration in the subject's lung.

2. The method of claim 1 , wherein the mRNA comprises a 5′ untranslated region.

3. The method of claim 2 , wherein the mRNA comprises a 3′ untranslated region.

4. The method of claim 3 , wherein the mRNA comprises a cap structure.

5. The method of claim 4 , wherein the mRNA comprises a poly A tail.

6. The method of claim 5 , wherein the lipid nanoparticle comprises one or more cationic lipids.

7. The method of claim 6 , wherein the lipid nanoparticle comprises one or more non-cationic lipids.

8. The method of claim 7 , wherein the mRNA is unmodified.

9. The method of claim 8 , wherein the composition is a reconstituted lyophilized composition.

10. The method of claim 7 , wherein the modification comprises a modified nucleotide.

11. The method of claim 10 , wherein the modified nucleotide is pseudouridine.

12. The method of claim 11 , wherein the composition is a reconstituted lyophilized composition.

13. The method of claim 1 , wherein the protein encoded by the mRNA is a polypeptide.

14. The method of claim 1 , wherein the protein encoded by the mRNA is a peptide.

15. The method of claim 8 , wherein the lipid nanoparticle has a size of less than about 100 nm.

16. The method of claim 11 , wherein the lipid nanoparticle has a size of less than about 100 nm.

17. The method of claim 8 , wherein the one or more PEG-modified lipids constitute from 0.1% to 20% of the total lipids by a molar ratio.

18. The method of claim 11 , wherein the one or more PEG-modified lipids constitute from 0.1% to 20% of the total lipids by a molar ratio.

19. The method of claim 5 , wherein the poly A tail comprises at least 90 nucleotides.

20. The method of claim 5 , wherein the poly A tail comprises at least 500 nucleotides.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 23, 2019
From: GUILD, BRAYDON CHARLES; DEROSA, FRANK; HEARTLEIN, MICHAEL
To: SHIRE HUMAN GENETIC THERAPIES, INC.
Reel/Frame 050804/0802 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 23, 2019
From: SHIRE HUMAN GENETIC THERAPIES, INC.
To: RANA THERAPEUTICS, INC.
Reel/Frame 050809/0609 →
CHANGE OF NAME Recorded Oct 23, 2019
From: RANA THERAPEUTICS, INC.
To: TRANSLATE BIO, INC.
Reel/Frame 050809/0668 →
Cited By (4)
US 12,378,560 US 12,458,604 US 12,576,040 US 12,691,166