IP Library Granted Patent US 10,501,512
Granted Patent B2
US 10,501,512 · App. 14/390,097 · Granted Dec 10, 2019

Modified polynucleotides

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Quick Facts
Patent No.
US 10,501,512
App. No.
14/390,097
Granted
Dec 10, 2019
Kind
B2
Abstract

The invention relates to compositions and methods for the preparation, manufacture and therapeutic use of polynucleotides, primary transcripts and mmRNA molecules.

Claims (19)

1. A composition comprising:

a plurality of lipid nanoparticles comprising a cationic lipid, a PEGylated lipid, cholesterol, and a phospholipid, wherein the mean particle size of the plurality of lipid nanoparticles is 80 nm to 160 nm and the lipid nanoparticles encapsulate a polynucleotide,

wherein the polynucleotide comprises;

(a) a first region of linked nucleosides, said first region encoding factor IX, wherein said first region of linked nucleosides consists of nucleotides selected from 1-methyl-pseudouridine, cytidine, adenosine, and guanosine;

(b) a first flanking region located at the 5′-terminus of said first region comprising;

(i) a 5′-untranslated region (5′-UTR); and

(ii) 5′ terminal cap;

(c) a second flanking region located at the 3′-terminus of said first region comprising;

(i′) a 3′-untranslated region (3′-UTR); and

(ii′) a 3′-tailing sequence of linked nucleosides.

2. The composition of claim 1 , wherein the 3′-tailing sequence of linked nucleosides is selected from the group consisting of a poly-A tail of approximately 160 nucleotides and a polyA-G quartet.

3. The composition of claim 1 , wherein the 5′ terminal cap is selected from the group consisting of Cap0, Cap1, ARCA, inosine, N1-methyl-guanosine, 2′-fluoro-guanosine, 7-deaza-guanosine, 8-oxo-guanosine, 2-amino-guanosine, LNA-guanosine, and 2-azido-guanosine.

4. A pharmaceutical composition comprising the composition of claim 1 and an excipient.

5. The pharmaceutical composition of claim 4 , wherein the excipient is selected from a solvent, aqueous solvent, non-aqueous solvent, dispersion media, diluent, dispersion, suspension aid, surface active agent, isotonic agent, thickening or emulsifying agent, preservative, lipid, lipidoids liposome, lipid nanoparticle, core-shell nanoparticles, polymer, lipoplex peptide, protein, cell, hyaluronidase, and mixtures thereof.

6. The composition of claim 1 , where the cationic lipid is selected from DLin-DMA, DLin-K-DMA, DLin-KC2-DMA, 98N12-5, C12-200, DLin-MC3-DMA, DODMA, DSDMA, and DLenDMA.

7. The composition of claim 1 , wherein the 5′-UTR and the 3′-UTR are not derived from the same species.

8. The composition of claim 1 , wherein at least one of the 5′-UTR or the 3′-UTR is not derived from beta-globin.

9. The composition of claim 1 , wherein the nanoparticles comprise about 50 mol % cationic lipid, about 38.5% cholesterol, about 10% phospholipid and about 1.5% PEGylated lipid.

10. A method of producing factor IX in a mammalian cell, tissue or organism comprising administering to said cell, tissue or organism the pharmaceutical composition of claim 4 .

Assignments (4)
SECURITY INTEREST Recorded Nov 19, 2025
From: MODERNATX, INC.
To: ARES CAPITAL CORPORATION, AS AGENT
Reel/Frame 073634/0354 →
CHANGE OF NAME Recorded Sep 28, 2016
From: MODERNA THERAPEUTICS, INC.
To: MODERNATX, INC.
Reel/Frame 040168/0398 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 13, 2014
From: BANCEL, STEPHANE; CHAKRABORTY, TIRTHA; DE FOUGEROLLES, ANTONIN; ELBASHIR, SAYDA M., PHD; JOHN, MATTHIAS; ROY, ATANU; WHORISKEY, SUSAN; WOOD, KRISTY M.; HATALA, PAUL; EJEBE, KENECHI; ELLSWORTH, JEFF LYNN; GUILD, JUSTIN
To: MODERNA THERAPEUTICS, INC.
Reel/Frame 034166/0252 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 13, 2014
From: SCHRUM, JASON P.
To: MODERNA THERAPEUTICS, INC.
Reel/Frame 034166/0859 →