IP Library Granted Patent US 11,597,698
Granted Patent B2
US 11,597,698 · App. 17/324,426 · Granted Mar 7, 2023

Branched tail lipid compounds and compositions for intracellular delivery of therapeutic agents

Inventors: Kerry E. Benenato (Sudbury, MA); Mark Cornebise (Arlington, MA); Edward Hennessy (Westwood, MA); Ellalahewage S. Kumarasinghe (Medfield, MA)
Assignee: ModernaTX, Inc.
C07C229/24A61K9/1272A61K31/713A61K47/543A61K48/005A61K48/0033
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Quick Facts
Patent No.
US 11,597,698
App. No.
17/324,426
Granted
Mar 7, 2023
Kind
B2
Abstract

The disclosure features novel lipids and compositions involving the same. Lipid nanoparticles (e.g., empty LNPs or loaded LNPs) include a novel lipid as well as additional lipids such as phospholipids, structural lipids, and PEG lipids. Lipid nanoparticles (e.g., empty LNPs or loaded LNPs) further including therapeutic and/or prophylactics such as RNA are useful in the delivery of therapeutic and/or prophylactics to mammalian cells or organs to, for example, regulate polypeptide, protein, or gene expression.

Claims (64)

1. A compound of Formula (A) or (B):

or its N-oxide, or a salt or isomer thereof,

wherein R′ a is R′ branched or R′ cyclic ; wherein

R′ branched is:

R′ cyclic is:

wherein

denotes a point of attachment;

wherein R aα is H, and R aβ , R aγ , and R aδ are each independently selected from the group consisting of H, C 2-12 alkyl, and C 2-12 alkenyl, wherein at least one of R aβ , R aγ , and R aδ is selected from the group consisting of C 2-12 alkyl and C 2-12 alkenyl;

R aα , R aβ , R aγ , and R aδ are each independently selected from the group consisting of H, C 2-30 alkyl, and C 5-20 alkenyl, wherein at least one of R aα , R aβ , R aγ , and R aδ is selected from the group consisting of C 2-30 alkyl and C 5-20 alkenyl;

R 2 and R 3 are each C 1-14 alkyl;

R 4 is selected from the group consisting of —(CH 2 )OH, —(CH 2 ) 3 OH, —(CH 2 ) 4 OH, —(CH 2 ) 5 OH and

wherein R 10 is N(R) 2 ; each R is independently selected from the group consisting of C 1-6 alkyl, C 2-3 alkenyl, and H; and n2 is selected from the group consisting of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10;

each R 5 is independently selected from the group consisting of OH, C 1-3 alkyl, C 2-3 alkenyl, and H;

each R 6 is independently selected from the group consisting of OH, C 1-3 alkyl, C 2-3 alkenyl, and H;

R 7 is H;

M and M′ are each independently selected from the group consisting of —C(O)O— and —OC(O)—;

R′ is a C 1-12 alkyl or C 2-12 alkenyl;

Y a is a C 3-6 carbocycle;

R*″ a is selected from the group consisting of C 1-15 alkyl and C 2-15 alkenyl;

1 is selected from the group consisting of 1, 2, 3, 4, and 5;

s is 2 or 3; and

m is selected from the group consisting of 5, 6, 7, 8, 9, 10, 11, 12, and 13.

2. The compound of claim 1 , wherein R aγ is a C 2-6 alkyl.

3. The compound of claim 1 , wherein the compound is of Formula (B) and R bγ is a C 2-6 alkyl.

4. The compound of claim 1 , wherein Y a is cyclohexyl or cyclopentyl, and R*″ a is a C 2 -alkyl or C 3 -alkyl.

5. An empty lipid nanoparticle (empty LNP), comprising about 40 mol % to about 60 mol % of a compound of claim 1 , about 0 mol % to about 20 mol % phospholipid, about 30 mol % to about 50 mol % structural lipid, and about 0 mol % to about 5 mol % PEG lipid.

6. The empty LNP of claim 5 , wherein the phospholipid is selected from the group consisting of:

1,2-dilinoleoyl-sn-glycero-3-phosphocholine (DLPC),

1,2-dimyristoyl-sn-glycero-phosphocholine (DMPC), 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC), 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC),

1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC),

1,2-diundecanoyl-sn-glycero-phosphocholine (DUPC),

1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC),

1,2-di-O-octadecenyl-sn-glycero-3-phosphocholine (18:0 Diether PC),

1-oleoyl-2-cholesterylhemisuccinoyl-sn-glycero-3-phosphocholine (OChemsPC),

1-hexadecyl-sn-glycero-3-phosphocholine (C16 Lyso PC),

1,2-dilinolenoyl-sn-glycero-3-phosphocholine, 1,2-diarachidonoyl-sn-glycero-3-phosphocholine,

1,2-didocosahexaenoyl-sn-glycero-3-phosphocholine, 1,2-dioleoyl-sn-glycero-3-phosphoethanola mine (DOPE), 1,2-diphytanoyl-sn-glycero-3-phosphoethanolamine (ME 16.0 PE),

1,2-distearoyl-sn-glycero-3-phosphoethanolamine,

1,2-dilinoleoyl-sn-glycero-3-phosphoethanolamine,

1,2-dilinolenoyl-sn-glycero-3-phosphoethanolamine,

1,2-diarachidonoyl-sn-glycero-3-phosphoethanolamine,

1,2-didocosahexaenoyl-sn-glycero-3-phosphoethanolamine,

1,2-dioleoyl-sn-glycero-3-phospho-rac-(1-glycerol) sodium salt (DOPG), sphingomyelin, and mixtures thereof.

7. The empty LNP of claim 5 , wherein the structural lipid is selected from the group consisting of cholesterol, fecosterol, sitosterol, ergosterol, campesterol, stigmasterol, brassicasterol, and mixtures thereof.

8. The empty LNP of claim 5 , wherein the PEG lipid is selected from the group consisting of a PEG-modified phosphatidylethanolamine, a PEG-modified phosphatidic acid, a PEG-modified ceramide, a PEG-modified dialkylamine, a PEG-modified diacylglycerol, a PEG-modified dialkylglycerol and mixtures thereof.

9. The empty LNP of claim 5 , wherein the PEG lipid is selected from PEG 2k- DMG and PEG-1:

and mixtures thereof.

10. A loaded lipid nanoparticle (loaded LNP), which comprises the empty LNP of claim 5 and one or more therapeutic and/or prophylactic agents.

11. The loaded LNP of claim 10 , wherein the one or more therapeutic and/or prophylactic agents is a nucleic acid.

12. The loaded LNP of claim 11 , wherein the nucleic acid is an RNA, and wherein the RNA is selected from the group consisting of a short interfering RNA (siRNA), an asymmetrical interfering RNA (aiRNA), a RNA interference (RNAi) molecule, a microRNA (miRNA), an antagomir, an antisense RNA, a ribozyme, a Dicer-substrate RNA (dsRNA), a small hairpin RNA (shRNA), a messenger RNA (mRNA), and mixtures thereof.

13. The loaded LNP of claim 12 , wherein the RNA is an mRNA.

14. A pharmaceutical composition comprising the loaded LNP claim 10 and a pharmaceutically acceptable carrier.

15. A method of delivering a therapeutic and/or prophylactic agent to a cell within a subject, the method comprising administering to the subject the loaded LNP of claim 10 .

16. A method of producing a polypeptide of interest in a cell within a subject, the method comprising administering to the subject the loaded LNP of claim 11 .

17. A method of treating a disease or disorder in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of the loaded LNP of claim 10 .

18. The compound of claim 1 , wherein R′ a is R′ branched .

19. The compound of claim 1 , wherein R 4 is selected from the group consisting of

—(CH 2 ) 2 OH, —(CH 2 ) 3 OH, —(CH 2 ) 4 OH, and —(CH 2 ) 5 OH.

20. The compound of claim 19 , wherein R 4 is —(CH 2 ) 2 OH.

21. The compound of claim 1 , wherein R 4 is

22. The compound of claim 1 , wherein the compound is a compound of Formula (A).

23. The compound of claim 1 , wherein the compound is a compound of Formula (B).

24. A compound selected from:

or its N-oxide, or a salt or isomer thereof.

Assignments (2)
SECURITY INTEREST Recorded Nov 19, 2025
From: MODERNATX, INC.
To: ARES CAPITAL CORPORATION, AS AGENT
Reel/Frame 073634/0354 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 19, 2021
From: BENENATO, KERRY E.; CORNEBISE, MARK; HENNESSY, EDWARD; KUMARASINGHE, ELLALAHEWAGE S.
To: MODERNATX, INC.
Reel/Frame 056288/0615 →
Cited By (4)
US 12,552,738 US 12,583,816 US 12,667,627 US 12,678,515