IP Library Granted Patent US 8,642,564
Granted Patent B2
US 8,642,564 · App. 12/036,963 · Granted Feb 4, 2014

Compositions for drug administration

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Quick Facts
Patent No.
US 8,642,564
App. No.
12/036,963
Granted
Feb 4, 2014
Kind
B2
Abstract

A composition having at least one alkyl glycoside and at least one therapeutic agent, wherein the alkylglycoside has an alkyl chain length from about 10 to about 16 carbon atoms and wherein the therapeutic agent is an oligonucleotide.

Claims (16)

1. A method of increasing the bioavailability of an oligonucleotide in a subject by administering a composition comprising the oligonucleotide and an absorption increasing amount of an alkylglycoside to the subject via an oral, rectal or gastrointestinal delivery route, wherein the alkylglycoside comprises a maltose linked by glycosidic linkage to an alkyl chain comprising between 10 to 16 carbons, thereby increasing the bioavailability of the oligonucleotide in the subject.

2. The method of claim 1 , wherein the oligonucleotide is an RNA interference molecule.

3. The method of claim 1 , wherein the oligonucleotide is an antisense oligonucleotide.

4. The method of claim 1 , wherein the oligonucleotide contains one or more phosphorothioate linkages.

5. The method of claim 1 , wherein the alkylglycoside is selected from the group consisting of dodecyl maltoside, tridecyl maltoside, and tetradecyl maltoside.

6. The method of claim 1 , wherein the alkylglycoside is tetradecyl-beta-D-maltoside.

7. The method of claim 1 , wherein the oligonucleotide has a molecular weight from about 5-10 kD.

8. The method of claim 1 , wherein the alkylglycoside is dodecyl-beta-D-maltoside.

9. The method of claim 1 , wherein the composition further comprises citric acid, sodium citrate, propylene glycol, glycerin, ascorbic acid, sodium metabisulfite, ethylenediaminetetraacetic acid (EDTA), benzalkonium chloride, sodium hydroxide, or combinations thereof.

10. The method of claim 9 , wherein the composition further comprises ethylenediaminetetraacetic acid (EDTA).

11. The method of claim 1 , wherein the composition is administered via the oral delivery route.

12. The method of claim 1 , wherein the composition is administered via the rectal delivery route.

13. The method of claim 1 , wherein the composition is administered via the gastrointestinal delivery route.

14. The method of claim 1 , wherein the alkylglycoside is present in the composition at a concentration of 0.01% to 20% by weight.

15. The method of claim 1 , wherein the oligonucleotide comprises a modified sugar moiety, a modified base moiety, a modified sugar linking moiety, or combination thereof.

16. The method of claim 1 , wherein the oligonucleotide comprises a modified linkage selected from the group consisting of phosphoramide, phosphorothioate, phosphorodithioate, methyl phosphonate, phosphotriester, phosphoramidate, O-methylphosphoroamidite, peptide, and combinations thereof.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Nov 14, 2024
From: ORBIMED ROYALTY & CREDIT OPPORTUNITIES III, LP
To: NEURELIS, INC.; AEGIS THERAPEUTICS, LLC
Reel/Frame 069359/0921 →
SECURITY INTEREST Recorded Aug 6, 2021
From: NEURELIS, INC.; AEGIS THERAPEUTICS, LLC
To: ORBIMED ROYALTY & CREDIT OPPORTUNITIES III, LP
Reel/Frame 057111/0242 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 5, 2008
From: MAGGIO, EDWARD T.
To: AEGIS THERAPEUTICS, LLC
Reel/Frame 020902/0419 →