IP Library Granted Patent US 8,632,785
Granted Patent B2
US 8,632,785 · App. 11/289,820 · Granted Jan 21, 2014

Clostridial toxin pharmaceutical composition containing a gelatin fragment

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Quick Facts
Patent No.
US 8,632,785
App. No.
11/289,820
Granted
Jan 21, 2014
Kind
B2
Abstract

A botulinum toxin pharmaceutical formulation comprising a botulinum toxin and a low molecular weight recombinant or native gelatin fragment suitable for administration to a human patient, and methods for treating patients with various diseases and afflictions using the formulation.

Claims (22)

1. A pharmaceutical composition, comprising:

(a) a botulinum toxin type A having a theoretical potency, and;

(b) a recombinantly made gelatin with a molecular weight between about 8 kD and about 100 kD, a buffer to adjust and maintain the pH between about 5.5 and about 6.5; and

wherein the pharmaceutical composition has a recovered potency of at least about 85% of the theoretical potency upon reconstitution with an aqueous solution subsequent to lyophilizing or vacuum drying.

2. The pharmaceutical composition of claim 1 , wherein the botulinum toxin is present as a botulinum toxin complex.

3. The pharmaceutical composition of claim 1 , wherein the botulinum toxin is present as a pure botulinum toxin.

4. A pharmaceutical composition, comprising:

(a) a botulinum toxin type A having a theoretical potency, and;

(b) a recombinant gelatin fragment with a molecular weight between about 25 kD and about 100 kD, a buffer to adjust and maintain the pH between about 5.5 and about 6.5;

wherein the pharmaceutical composition has a recovered potency of at least about 85% of the theoretical potency upon reconstitution with an aqueous solution subsequent to lyophilizing or vacuum drying.

5. A pharmaceutical composition comprising:

(a) a botulinum toxin type A having a theoretical potency, and;

(b) a recombinant gelatin with a molecular weight of between about 25 kD and about 100 kD, a buffer to adjust and maintain the pH between about 5.5 to about 6.5, wherein the pharmaceutical composition has a recovered potency of between about 80% and about 120% of the theoretical potency upon reconstitution with an aqueous solution subsequent to lyophilizing or vacuum drying.

6. A pharmaceutical composition, comprising:

(a) a botulinum toxin type A having a theoretical potency;

(b) a recombinant gelatin fragment with a molecular weight between about 8 kD and about 100 kD, and;

(c) a buffer to adjust and maintain the pH,

wherein the botulinum toxin present in the pharmaceutical composition has a recovered potency of at least about 80% of the theoretical potency upon reconstitution with an aqueous solution subsequent to lyophilizing or vacuum drying and wherein the pharmaceutical composition is free of animal-derived products.

7. A pharmaceutical composition, comprising:

(a) a botulinum toxin type A having a theoretical potency, and;

(b) at least one plurality of recombinant gelatin fragment selected from the group consisting of recombinant gelatin fragments of molecular weights about 8.5 kD, about 25 kD, and about 50 kD; and a buffer to adjust and maintain the pH to about 6.5;

wherein the the pharmaceutical composition has a recovered potency of at least about 100% of the theoretical potency upon reconstitution with an aqueous solution subsequent to lyophilizing or vacuum drying.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 25, 2006
From: HUNT, TERRENCE J.
To: ALLERGAN, INC.
Reel/Frame 017210/0563 →