IP Library Patent Application 12590154
Patent Application
App. No. 12/590,154

Compositions of activated botulinum holotoxin type B (150 kD)

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Patent No.
US None
App. No.
12/590,154
Abstract

The present invention relates to pharmaceutical compositions of activated botulinum holotoxin type B (150 kD). In particular, the present invention relates to botulinum toxin type B pharmaceutical compositions wherein at least 90% of said botulinum toxin type B is activated (i.e., “nicked”), and wherein at least 99% said nicked botulinum toxin type B is a 150 kD holotoxin (i.e., “stripped”). The invention also relates to a process of activating and stripping botulinum toxin type B wherein at least 90% of said botulinum toxin type B is nicked, and wherein at least 99% of said nicked botulinum toxin type B is stripped. The invention further relates to methods for the treatment of a variety of neuromuscular diseases, pain, inflammatory and cutaneous disorders comprising administering a pharmaceutical composition of activated botulinum holotoxin type B (150 kD) wherein at least 90% of said botulinum toxin type B is nicked, and wherein at least 99% of said nicked botulinum toxin type B is stripped.

Claims (41)

1 . A pharmaceutical composition comprising:

(a) activated botulinum toxin type B; and

(b) at least one excipient;

wherein at least 90% of said botulinum toxin type B is nicked; and

wherein at least 99% of said nicked botulinum toxin type B is an approximately 150 kD holotoxin.

2 . The pharmaceutical composition of claim 1 , wherein greater than 90 percent of said botulinum toxin B is nicked.

3 . The pharmaceutical composition of claim 1 , wherein approximately about 95 percent to about 100 percent of said botulinum toxin type B is nicked.

4 . The pharmaceutical composition of claim 1 , wherein greater than 95 percent of said botulinum toxin B is nicked.

5 . The pharmaceutical composition of claim 1 , wherein greater than 99 percent of said botulinum toxin B is nicked.

6 . The pharmaceutical composition of claim 1 , wherein greater than 99 percent of said botulinum toxin B is stripped.

7 . The pharmaceutical composition of claim 1 , wherein said at least one excipient is selected from the group consisting of: buffers, carriers, stabilizers, preservatives, diluents, vehicles, bulking agents, albumins, gelatins, collagens, proteins, polysaccharides, metals, non-oxidizing amino acid derivatives, and sodium chloride.

8 . The pharmaceutical composition of claim 7 , wherein said at least one excipient is albumin.

9 . The pharmaceutical composition of claim 7 , wherein said at least one excipient is a buffer.

10 . The pharmaceutical composition of claim 9 , wherein said buffer is a succinate buffer.

11 . A process of activating and stripping botulinum toxin type B, comprising the stages of:

cell growth, activation, purification, and dilution; wherein at least one protease is administered to a volume of said botulinum toxin type B; wherein said protease administered increases the levels of nicked botulinum toxin type B to at least 90%;

wherein at least one dissociating reagent is administered to a volume of said nicked botulinum toxin type B; and wherein said dissociating reagent administered increases the levels of stripped botulinum toxin type B to at least 99%.

12 . The process of claim 11 , wherein said at least one protease administered is selected from the group consisting of: trypsin, immobilized TPCK-trypsin, metalloproteases, endogenous proteases, bacterial proteases, plant derived proteases, and gastric proteases.

13 . The process of claim 12 , wherein said protease administered is animal free trypsin.

14 . The process of claim 11 , wherein said at least one dissociating reagent administered is a succinate buffer.

15 . The process of claim 11 , wherein greater than 90 percent of said botulinum toxin B is nicked.

16 . The process of claim 11 , wherein approximately about 95 percent to about 100 percent of said botulinum toxin type B is nicked.

17 . The process of claim 11 , wherein greater than 95 percent of said botulinum toxin B is nicked.

18 . The process of claim 11 , wherein greater than 99 percent of said botulinum toxin B is nicked.

19 . The process of claim 11 , wherein greater than 99 percent of said botulinum toxin B is stripped.

20 . A method of treating a variety of disorders, comprising administering to a patient in need thereof, a pharmaceutical composition comprising:

(a) activated botulinum toxin type B; and

(b) at least one excipient;

wherein at least 90% of said botulinum toxin type B is nicked; and

wherein at least 99% of said nicked botulinum toxin type B is stripped.

21 . The method of claim 20 , wherein greater than 90 percent of said botulinum toxin B in said pharmaceutical composition is nicked.

22 . The method of claim 20 , wherein approximately about 95 percent to about 100 percent of said botulinum toxin type B in said pharmaceutical composition is nicked.

23 . The method of claim 20 , wherein greater than 95 percent of said botulinum toxin B in said pharmaceutical composition is nicked.

24 . The method of claim 20 , wherein greater than 99 percent of said botulinum toxin B in said pharmaceutical composition is nicked.

25 . The method of claim 20 , wherein greater than 99 percent of said botulinum toxin B in said pharmaceutical composition is stripped.

26 . The method of claim 20 , wherein said at least one excipient of said pharmaceutical composition is selected from the group consisting of: buffers, carriers, stabilizers, preservatives, diluents, vehicles, bulking agents, albumins, gelatins, collagens, proteins, polysaccharides, metals, non-oxidizing amino acid derivatives, and sodium chloride.

27 . The method of claim 26 , wherein said at least one excipient of said pharmaceutical composition is albumin.

28 . The method of claim 26 , wherein said at least one excipient of said pharmaceutical composition is a buffer.

29 . The method of claim 28 , wherein said buffer is a succinate buffer.

30 . The method of claim 20 , wherein said disorder is selected from the group consisting of:

opthalmologic disorders, neuromuscular diseases, otorhinolaryngological disorders, urogenital disorders, dermatological disorders, pain disorders, inflammatory disorders, secretory disorders, and cutaneous disorders or cosmetic treatment.

Assignments (4)
NOTICE OF RELEASE OF SECURITY INTEREST Recorded Nov 30, 2015
From: JPMORGAN CHASE BANK, N.A.
To: SOLSTICE NEUROSCIENCES, LLC
Reel/Frame 037171/0795 →
SECURITY AGREEMENT Recorded Sep 26, 2012
From: SOLSTICE NEUROSCIENCES, LLC
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 029041/0720 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 29, 2011
From: SOLSTICE NEUROSCIENCES, INC.
To: SOLSTICE NEUROSCIENCES, LLC
Reel/Frame 027295/0296 →
CORRECTIVE ASSIGNMENT TO CORRECT THE PROPERTY NUMBERS PREVIOUSLY RECORDED ON REEL 024684 FRAME 0992. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT.. Recorded Jul 15, 2010
From: GARCIA, SHERYL ANN; MARIN, BRET; JOSEPH, SHAJI
To: SOLSTICE NEUROSCIENCES, INC.
Reel/Frame 024687/0545 →