IP Library Granted Patent US 8,241,640
Granted Patent B2
US 8,241,640 · App. 12/073,245 · Granted Aug 14, 2012

Pharmaceutical botulinum toxin compositions

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Quick Facts
Patent No.
US 8,241,640
App. No.
12/073,245
Granted
Aug 14, 2012
Kind
B2
Abstract

Botulinum toxin, a well know systemic poison, produces favorable therapeutic effect by virtue of regionally attaching to nerves within the myoneural junction and possibly other tissues in a target region of a particular tissue. The present invention provides compositions of botulinum toxin and a sequestration agent that increase sequestration and delivery of the botulinum toxin to neural and associated tissues, as compared with available formulations of botulinum toxins, and thereby produce a beneficial clinical effect. The sequestration agents of the present invention include proteins, lipids and carbohydrates. A preferred composition of the present invention comprises a botulinum toxin and an albumin. The present invention also provides methods of treating neuromuscular diseases and pain using the disclosed compositions and methods of making the disclosed compositions.

Claims (3)

1. A method of preparing a pharmaceutical composition comprising the steps of lyophilizing a composition comprising a botulinum toxin and optionally human serum albumin and optionally a stabilizing sugar and adding a quantity of human serum albumin to the lyophilized botulinum toxin composition in an amount sufficient to achieve between 13,000 and 50,500 μg human serum albumin per 100 LD 50 units botulinum toxin.

2. A method of preparing a pharmaceutical composition comprising the steps of lyophilizing a composition comprising a botulinum toxin and optionally human serum albumin and optionally a stabilizing sugar and adding a quantity of human serum albumin to the lyophilized botulinum toxin composition in an amount sufficient to achieve between 50,500 and 505,000 μg human serum albumin per 100 LD 50 units botulinum toxin.

3. A method of preparing a pharmaceutical composition comprising the steps of lyophilizing a composition comprising a botulinum toxin and optionally human serum albumin and optionally a stabilizing sugar and adding a quantity of human serum albumin to the lyophilized botulinum toxin composition in an amount sufficient to achieve between 50,500 and 90,500 μg human serum albumin per 100 LD 50 units botulinum toxin.

Assignments (7)
SECURITY INTEREST Recorded Feb 17, 2025
From: REVANCE THERAPEUTICS, INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 070239/0739 →
RELEASE OF SECURITY INTEREST Recorded Feb 7, 2025
From: ATHYRIUM BUFFALO LP
To: REVANCE THERAPEUTICS, INC
Reel/Frame 070153/0630 →
SECURITY INTEREST Recorded Feb 7, 2025
From: REVANCE THERAPEUTICS, INC.; CROWN LABORATORIES, INC.
To: HAYFIN SERVICES LLP, AS ADMINISTRATIVE AGENT
Reel/Frame 070153/0663 →
SECURITY INTEREST Recorded Feb 7, 2025
From: REVANCE THERAPEUTICS, INC.; BELLUS MEDICAL, LLC; CROWN LABORATORIES, INC.
To: HAYFIN SERVICES LLP, AS ADMINISTRATIVE AGENT
Reel/Frame 070153/0736 →
SECURITY INTEREST Recorded Mar 18, 2022
From: REVANCE THERAPEUTICS, INC.
To: ATHYRIUM BUFFALO LP
Reel/Frame 059437/0654 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 3, 2016
From: BOTULINUM TOXIN RESEARCH ASSOCIATES, INC.
To: REVANCE THERAPEUTICS, INC.
Reel/Frame 038870/0160 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 17, 2008
From: BORODIC, GARY E.
To: BOTULINUM TOXIN RESEARCH ASSOCIATES, INC.
Reel/Frame 021105/0406 →