IP Library Granted Patent US 9,808,481
Granted Patent B2
US 9,808,481 · App. 15/187,576 · Granted Nov 7, 2017

Prebiotic formulations and methods of use

Inventors: Andrew J. Ritter (Los Angeles, CA); Dennis Savaiano (West Lafayette, IN); David Barnes (Dexter, MI); Todd Klaenhammer (Raleigh, NC)
Assignee: Ritter Pharmaceuticals, Inc.
A61K31/715A23L33/135A23L33/21A61K9/4825A61K31/702A61K31/7004A61K31/7016A61K35/741A61K35/745A61K35/747A23V2002/00A23Y2220/00A23Y2300/00
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Quick Facts
Patent No.
US 9,808,481
App. No.
15/187,576
Granted
Nov 7, 2017
Kind
B2
Abstract

The invention provides methods and compositions for treating symptoms associated with lactose intolerance and for overall improvement in gastrointestinal health. Described herein are methods and compositions for improving overall gastrointestinal health or for decreasing symptoms of lactose intolerance by administering to subject in need thereof a prebiotic composition, optionally in combination with effective amount of a probiotic microbe or microbes.

Claims (17)

1. A pharmaceutical composition comprising: a GOS composition comprising at least 95% by weight galactooligosaccharides (GOS) and 5% or less by weight digestible saccharides, wherein the GOS composition comprises about 5-25% pentasaccharides.

2. The pharmaceutical composition of claim 1 , wherein the GOS composition does not contain a probiotic.

3. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition further comprises a pharmaceutically acceptable excipient.

4. The pharmaceutical composition of claim 1 , wherein the GOS composition comprises about 0.1 to about 20 g of GOS by weight.

5. The pharmaceutical composition of claim 1 , wherein said pharmaceutical composition comprises an enteric coating.

6. The pharmaceutical composition of claim 1 , wherein said dosage form is formulated for controlled release.

7. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition comprises less than about 10 ppm heavy metals.

8. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition comprises less than about 0.10% by weight sulphated ash.

9. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition further comprises a flavoring and/or colorant.

10. The pharmaceutical composition of claim 3 , wherein the excipient is silicone dioxide or microcrystalline cellulose.

11. The pharmaceutical composition of claim 5 , wherein the microcrystalline cellulose is silicified microcrystalline cellulose.

12. The pharmaceutical composition of claim 1 , wherein the GOS composition comprises about 5-20% pentasaccharides.

13. The pharmaceutical composition of claim 1 , wherein the GOS composition comprises about 5-15% pentasaccharides.

14. The pharmaceutical composition of claim 1 , wherein the GOS composition comprises about 5-10% pentasaccharides.

15. The pharmaceutical composition of claim 5 , wherein the GOS composition comprises about 5-20% pentasaccharides.

16. The pharmaceutical composition of claim 5 , wherein the GOS composition comprises about 5-15% pentasaccharides.

17. The pharmaceutical composition of claim 5 , wherein the GOS composition comprises about 5-10% pentasaccharides.

Continuity (6)
Continuation 14485301 · Sep 12, 2014
Continuation 13770750 · Feb 19, 2013
Continuation 12707037 · Feb 17, 2010
Provisional Application 61272622 · Oct 13, 2009
Provisional Application 61155150 · Feb 24, 2009
Related Publication 20160367579A1 · Dec 22, 2016