IP Library Granted Patent US 9,017,667
Granted Patent B2
US 9,017,667 · App. 13/123,219 · Granted Apr 28, 2015

Dosage forms that facilitate rapid activation of barley protease zymogen

Inventor: Bret Berner (Half Moon Bay, CA)
Assignee: Alvine Pharmaceuticals, Inc.
A61K38/4873A61K9/1623A61K9/2013A61K9/2077A61K9/2095A61K9/4858A61K9/5042A61K9/5084C12N9/50
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Quick Facts
Patent No.
US 9,017,667
App. No.
13/123,219
Granted
Apr 28, 2015
Kind
B2
Abstract

The therapeutic efficacy of zymogen proteins for oral administration is improved by including in the formulation one or more excipients that optimize pH and other reaction conditions for rapid activation of the zymogen shortly after ingestion.

Claims (17)

1. A unit dose of a dry pharmaceutical formulation for oral administration of an isolated barley EP-B2 protease zymogen, the formulation comprising:

an effective unit dose of said barley EP-B2 protease zymogen comprising protein content in the range of 10 to 80% of the formulation by weight; and

from 25 to 250 mg of an acid or acidic buffer system, which comprises one or more of

citric acid, maleic acid, malic acid, and fumaric acid and which provides a pH suitable for activation of EP-B2 protease zymogen when the formulation is exposed to gastric fluid;

formulated as capsules, particles or granules in capsules or sachets, or tablets.

2. The formulation of claim 1 , further comprising an antioxidant.

3. The formulation of claim 1 , further comprising a polymer.

4. The formulation of claim 3 , wherein the polymer is an anionic polymer.

5. The formulation of claim 4 , wherein the polymer is selected from the group consisting of dextran sulfate, chondroitin, chondroitin sulfate, heparin, heparin sulfate, cellulose sulfate, xanthan, hyaluronic acid, polyacrylic acid, polyacrylamide, carboxymethylcellulose, polypropanesulfonic acid, polyglutamates, anionic chitosan derivatives, and anionic maleic anhydride copolymers and derivatives.

6. The formulation of claim 5 , wherein the polymer is dextran sulfate at a dose of about 2 μg to about 100 μg.

7. The formulation of claim 1 , wherein the capsule is made of hypromellose.

8. The pharmaceutical formulation of claim 1 , wherein at least 20% of the acid or acidic buffer system is released within 15 minutes of immersing the pharmaceutical formulation in gastric fluid.

9. The pharmaceutical formulation of claim 1 , wherein at least 30% of the barley EP-B2 protease is released in a pulsatile or gradual release profile beginning at least 15 minutes after immersing the pharmaceutical formulation in gastric fluid.

10. A unit dose of a dry pharmaceutical formulation for oral administration of an isolated barley EP-B2 protease zymogen, the formulation comprising:

an effective unit dose of said barley EP-B2 protease zymogen comprising protein content in the range of 10 to 80% of the formulation by weight; and

from 25 to 250 mg of an acid or acidic buffer system, which comprises one or more of citric acid, maleic acid, malic acid, and fumaric acid, and from 1 to 100 mg of sodium metabisulfite;

formulated as capsules, particles or granules in capsules or sachets, or tablets.

Assignments (3)
SECURITY INTEREST Recorded Oct 14, 2022
From: IMMUNOGENX, INC.
To: MATTRESS LIQUIDATORS, INC.
Reel/Frame 061429/0816 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 30, 2016
From: ALVINE PHARMACEUTICALS, INC.
To: IMMUNOGENICS LLC
Reel/Frame 039060/0975 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 14, 2012
From: BERNER, BRET
To: ALVINE PHARMACEUTICALS, INC.
Reel/Frame 027703/0831 →
Continuity (2)
Provisional Application 61104607 · Oct 10, 2008
Related Publication 20110236369A1 · Sep 29, 2011