IP Library Granted Patent US 10,420,791
Granted Patent B2
US 10,420,791 · App. 15/625,648 · Granted Sep 24, 2019

CFTR MRNA compositions and related methods and uses

Inventors: Michael Heartlein (Cambridge, MA); Braydon Charles Guild (Concord, MA); Frank DeRosa (Cambridge, MA); Carsten Rudolph (Planegg, DE); Christian Plank (Planegg, DE); Lianne Smith (Cambridge, MA)
Assignee: Translate Bio, Inc.
A61K31/713A61K9/0073A61K9/0078A61K9/1271A61K9/5123A61K31/7105A61K31/7115A61K47/6935A61K48/005C07K14/705C12N9/14A61K9/127A61K48/00C07H21/02C07K14/4712C12N15/63C12N15/88C12Y306/03049
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Quick Facts
Patent No.
US 10,420,791
App. No.
15/625,648
Granted
Sep 24, 2019
Kind
B2
Abstract

The present invention is particularly useful for treating cystic fibrosis. The disclosure concerns method and compositions for treating cystic fibrosis. The method comprises inducing CFTR expression in epithelial cells in a lung of a mammal by contacting the epithelial cells in the lung of the mammal with a composition, where the composition is a pharmaceutical composition comprising in vitro transcribed mRNA.

Claims (14)

1. A method of producing cystic fibrosis transmembrane conductance regulator (CFTR) protein in a lung of a mammal, the method comprising:

administering to the lung of the mammal by aerosolization a composition comprising an mRNA-loaded nanoparticle, wherein the nanoparticle is a liposome, wherein the mRNA is an in vitro transcribed mRNA and has a coding sequence at least 80% identical to SEQ ID NO: 3, wherein the mRNA encodes a human CFTR protein comprising the amino acid sequence of SEQ ID NO:1, and wherein the mRNA is unmodified.

2. The method of claim 1 , wherein the mRNA has the coding sequence at least 90% identical to SEQ ID NO: 3.

3. The method of claim 1 , wherein the mRNA has the coding sequence 100% identical to SEQ ID NO: 3.

4. The method of claim 1 , wherein the mRNA comprises a 5′ untranslated region (UTR) and/or a 3′ UTR.

5. The method of claim 4 , wherein the 5′-UTR comprises SEQ ID NO: 4 and/or the 3′-UTR comprises SEQ ID NO: 5.

6. The method of claim 4 , wherein the mRNA further comprises a poly-A tail.

7. The method of claim 6 , wherein the poly-A tail is of at least 70, 100, 120, 150, 200, or 250 residues in length.

8. The method of claim 4 , wherein the mRNA further comprises a 5′ cap.

9. The method of claim 1 , wherein the aerosolization is nebulization.

10. The method of claim 1 , wherein the human CFTR protein is expressed in the epithelial cells of the lung.

11. The method of claim 1 , wherein the composition further comprises a pharmaceutically acceptable carrier.

12. The method of claim 1 , wherein the liposome comprises one or more PEGylated lipids.

13. The method of claim 1 , wherein the liposome further comprises one or more cationic lipids and one or more non-cationic lipids.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 25, 2018
From: HEARTLEIN, MICHAEL; GUILD, BRAYDON CHARLES; DEROSA, FRANK; SMITH, LIANNE
To: SHIRE HUMAN GENETIC THERAPIES, INC.
Reel/Frame 044732/0200 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 25, 2018
From: RUDOLPH, CARSTEN; PLANK, CHRISTIAN
To: ETHRIS GMBH
Reel/Frame 044732/0233 →
CHANGE OF NAME Recorded Jan 25, 2018
From: RANA THERAPEUTICS, INC.
To: TRANSLATE BIO, INC.
Reel/Frame 045153/0801 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 25, 2018
From: SHIRE HUMAN GENETIC THERAPIES, INC.
To: RANA THERAPEUTICS, INC.
Reel/Frame 045153/0805 →
Continuity (5)
Division 14876071 · Oct 6, 2015
Division 14307322 · Jun 17, 2014
Continuation PCTUS2014028849 · Mar 14, 2014
Provisional Application 61783663 · Mar 14, 2013
Related Publication 20180015116A1 · Jan 18, 2018
Cited By (2)
US 12,458,604 US 12,576,040