IP Library Granted Patent US 11,278,498
Granted Patent B2
US 11,278,498 · App. 17/089,956 · Granted Mar 22, 2022

Sustained release solid dosage forms for modulating the colonic microbiome

Inventors: Ryan Barrett (Acton, MA); Hitesh Bhagat (Framingham, MA); Anthony Stewart Campbell (Framingham, MA)
Assignee: Axial Therapeutics, Inc.
A61K9/2013A61K9/2009A61K9/2018A61K9/2027A61K9/2054A61K9/2813A61K9/2826A61K9/2846A61K9/2866A61K9/485A61K9/4858A61K9/4866A61K9/501A61K9/5015A61K9/5026A61K9/5042A61K31/353
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Quick Facts
Patent No.
US 11,278,498
App. No.
17/089,956
Granted
Mar 22, 2022
Kind
B2
Abstract

Described are sustained-release solid dosage forms of epigallocatechin gallate (EGCG) or aminosterol compositions. In one aspect of the invention the sustained-release solid dosage forms of EGCG or an aminosterol are capsules comprising a plurality of coated solid particulates. Another aspect of the invention relates to methods of inhibiting, ameliorating, reducing the likelihood of, delaying the onset of, treating or preventing an amyloid disorder, comprising the step of administering to a subject in need a therapeutically effective amount of the solid dosage form. In certain aspects, the amyloid disorder is Parkinson's Disease.

Claims (21)

1. A sustained-release solid dosage form of epigallocatechin gallate (EGCG), comprising a plurality of solid particulates selected from the group consisting of mini-tablets, beads, granules, and pellets, or being in a form of a single solid dosage form, and wherein the solid particulates or the single solid dosage form each comprise(s):

a core comprising EGCG and a

release rate controlling material selected from the group consisting of polyethylene oxide, poly(acrylic acid), methacrylic ester copolymer, alkylammonium methacrylate copolymer, and hydroxypropyl methyl cellulose;

wherein the sustained-release solid dosage form releases 10-50% of the EGCG within 24 hours, 30-80% of the EGCG within 48 hours, and at least 60% of the EGCG within 72 hours of administration of said dosage form to a human subject;

wherein the sustained-release solid dosage form comprises a total amount of EGCG in the range of about 50 mg to about 1,000 mg; and

wherein the EGCG has a purity of at least 98%.

2. The sustained-release solid dosage form of claim 1 , wherein the core comprises: (a) EGCG, (b) poly(acrylic acid), (c) colloidal silicon dioxide, and (d) magnesium stearate.

3. The sustained-release solid dosage form of claim 2 , wherein the weight ratio of (a):(b):(c):(d) in the core is about 58.6:39:1.2:1.

4. The sustained-release solid dosage form of claim 1 , wherein the core comprises: (a) EGCG, (b) polyethylene oxide, (c) colloidal silicon dioxide, and (d) sodium stearyl fumarate.

5. The sustained-release solid dosage form of claim 4 , wherein the weight ratio of (a):(b):(c):(d) in the core is about 19.3:77.2:1.2:2.3.

6. The sustained-release solid dosage form of claim 1 , wherein the core comprises: (a) EGCG, (b) poly(acrylic acid), (c) talc, and (d) magnesium stearate.

7. The sustained-release solid dosage form of claim 6 , wherein the weight ratio of (a):(b):(c):(d) in the core is about 65.3:32.7:1:1.

8. The sustained-release solid dosage form of claim 1 , wherein the core comprises: (a) EGCG, (b) methacrylic ester copolymer, alkylammonium methacrylate copolymer, or a combination thereof, (c) colloidal silicon dioxide, and (d) magnesium stearate.

9. The sustained-release solid dosage form of claim 8 , wherein the weight ratio of (a):(b):(c):(d) in the core is about 32.7:65.3:1:1.

10. The sustained-release solid dosage form of claim 8 , comprising a coating on the solid particulates, wherein the coating comprises methacrylic ester copolymer, alkylammonium methacrylate copolymer, or a combination thereof.

11. The sustained-release solid dosage form of claim 10 , wherein the weight ratio of the coating to the core is about 8:100 to about 10:100.

12. The sustained-release solid dosage form of claim 1 , wherein the core comprises: (a) EGCG, (b) methacrylic ester copolymer, alkylammonium methacrylate copolymer, or a combination thereof, (c) colloidal silicon dioxide, and (d) sodium stearyl fumarate.

13. The sustained-release solid dosage form of claim 12 , wherein the weight ratio of (a):(b):(c):(d) in the core is about 32:64.1:1.3:2.6.

14. The sustained-release solid dosage form of claim 1 , wherein the administration is oral administration.

15. The sustained-release solid dosage form of claim 1 , wherein the total amount of EGCG is in the range of about 50 mg to about 200 mg.

16. The sustained-release solid dosage form of claim 1 , wherein the total amount of EGCG is in the range of about 100 mg to about 300 mg.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 15, 2022
From: BARRETT, RYAN; BHAGAT, HITESH; CAMPBELL, ANTHONY STEWART
To: AXIAL THERAPEUTICS, INC.
Reel/Frame 059607/0221 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 22, 2021
From: BARRETT, RYAN; BHAGAT, HITESH; CAMPBELL, ANTHONY STEWART
To: AXIAL THERAPEUTICS, INC.
Reel/Frame 055998/0468 →
Continuity (5)
Continuation PCTUS2020031718 · May 6, 2020
Provisional Application 62844016 · May 6, 2019
Provisional Application 62844013 · May 6, 2019
Provisional Application 62844006 · May 6, 2019
Related Publication 20210052503A1 · Feb 25, 2021