IP Library Patent Application 17683171
Patent Application
App. No. 17/683,171

NUCLEIC ACID VACCINES

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Quick Facts
Patent No.
US None
App. No.
17/683,171
Abstract

The invention relates to compositions and methods for the preparation, manufacture and therapeutic use ribonucleic acid vaccines (NAVs) comprising polynucleotide molecules encoding one or more antigens.

Claims (16)

1 - 23 . (canceled)

24 . A method of vaccinating a subject comprising administering to the subject at least one dose of a nucleic acid vaccine comprising one or more mRNA polynucleotides comprising at least one chemical modification comprising an open reading frame encoding a viral surface polypeptide antigen and a lipid nanoparticle wherein the lipid nanoparticle comprises cationic lipid, non-cationic lipid, structural lipid, and PEG-modified lipid.

25 . The method of claim 24 , wherein the method produces neutralizing antibodies in the subject within three weeks of a single administration.

26 . The method of claim 24 , wherein the method comprises administering to the subject a single dosage of between 0.001 mg/kg and 0.005 mg/kg of the nucleic acid vaccine.

27 . The method of claim 24 , wherein the chemical modification is selected from of pseudouridine, N1-methylpseudouridine, 5-methylcytosine and 5-methoxyuridine.

28 . The method of claim 24 , wherein the chemical modification is a N1-methylpseudouridine.

29 . The method of claim 24 , wherein the vaccine is monovalent.

30 . The method of claim 24 , wherein the mRNA polynucleotide has at least two chemical modifications.

31 . The method of claim 24 , wherein the open reading frame is codon-optimized.

32 . The method of claim 24 , wherein the polynucleotide comprises a poly-A tail of 40-200 nucleotides in length.

33 . The method of claim 24 , wherein the nucleic acid vaccine is multivalent comprising one or more mRNA polynucleotides each having an open reading frame.

34 . The method of claim 24 , wherein the lipid nanoparticle comprises about 40-60% cationic lipid: about 5-15% non-cationic lipid: about 30-50% structural lipid; and about 1-2% PEG-modified lipid.

35 . The method of claim 34 , wherein the structural lipid is cholesterol.

36 . The method of claim 24 , further comprising administering more than one dose of the vaccine.

37 . The method of claim 36 , wherein the doses are administered 2 weeks, 3 weeks, 1 month, or 2 months apart.

38 . The method of claim 24 , wherein the vaccine is administered to the subject by intramuscular injection.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 11, 2022
From: CIARAMELLA, GUISEPPE; HUANG, ERIC YI-CHUN; BOUCHON, AXEL
To: MODERNATX, INC.
Reel/Frame 059235/0898 →