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Botulinum Toxin and the Treatment of Primary Disorders of Mood and Affect

a neurotoxin and mood and affect technology, applied in the field of treating primary disorders of mood and affect with neurotoxins, can solve the problems of ssris causing numerous side effects, affecting the normal functioning of the brain, so as to reduce agitation, reduce agitation, and reduce the effect of at least one central nervous system neurotransmitter

Inactive Publication Date: 2015-10-22
REVANCE THERAPEUTICS INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The present invention provides methods for treating anxiety disorders and neurodegenerative diseases associated with inflammation by administering a composition containing a neurotoxin to decrease cholinergic neuron transmission in the central nervous system. The methods involve delivering the neurotoxin to the central nervous system through various methods such as injection or topical application. The invention also provides pharmaceutical compositions for delivering a botulinum toxin based pharmaceutical to the central nervous system. The methods and pharmaceutical compositions can lead to reduced symptoms of anxiety disorders and neurodegenerative diseases associated with inflammation.

Problems solved by technology

Major depression is a particularly disabling and pernicious, in part, because it is recurring.
As a consequence of numerous dietary restrictions associated with the use of monoamine oxidase inhibitors, extensive side effects, including hypertension, headache, myoclonic jerk, sleep disruption, and gastrointestinal complications, monoamine oxidase inhibitors are currently not used as a first-line antidepressant.
Although generally milder than the monoamine oxidase inhibitors and the tricyclic antidepressants, SSRIs also produce numerous side effects.
Direct injection into the brain is not practical and in fact unlikely to be conventionally practiced by a physician skilled in the treatment of seizure disorders because of the possibility and risk associated with induced hemorrhage, scarring, neuronal loss and placement difficulty, infection (meningitis) and inconvenience associated with necessary delivery mechanisms.
Direct injection into the CNS is highly impractical because of such complications associated with invasive intracranial procedures.
Despite this suggestion, controlled trials using small numbers of patients in the study groups, have failed to demonstrate the efficacy of botulinum toxin for the treatment of myofascial and other forms of pain.
The ineffectiveness of botulinum toxin to treat a variety of pain syndromes, in controlled trial, has been attributed to small sample size and relatively low statistical power.
The statistical significance of these results, however, was uncertain, inconsistent between treatment groups, and exhibited unexplained inverted dose response curves.

Method used

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  • Botulinum Toxin and the Treatment of Primary Disorders of Mood and Affect

Examples

Experimental program
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Effect test

example 1

[0077]A 78-year-old male who noted sleep disturbances and anxiety was initially diagnosed with blepharospasm. Botulinum toxin was administered by injection, and the subject noted improved sleep and reduced anxiety.

example 2

[0078]A 44-year-old bus driver was diagnosed with hemifacial spasm and reported symptoms of anxiety. Botulinum toxin was administered by injection. The subject noted a better ability to cope with work-related stresses and cope with difficult situations with less stress.

example 3

[0079]A 72-year-old consultant diagnosed with hemifacial spasm who reported sleep disturbances and anxiety was treated with botulinum toxin that was administered by injection. The subject reported improved sleep and reduced anxiety and less agitation.

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Abstract

A method of treating depression includes identifying a subject with a pain syndrome for increased responsiveness to the treatment of pain associated with the pain syndrome with botulinum toxin and locally administering a botulinum toxin subcutaneously to a face of the subject, thereby treating said pain. Identification of the pain is made prior to administering botulinum toxin for the treatment of said pain. The subject has a pain syndrome and a condition selected from the group consisting of a depressive disorder, an anxiety disorder and a sleep disorder.

Description

[0001]This application claims benefit to U.S. Provisional Application Ser. No. 60 / 690,162, filed on Jun. 14, 2005; U.S. Provisional Application Ser. No. 60 / 693,771, filed on Jun. 27, 2005; U.S. Provisional Application Ser. No. 60 / 721,060, filed on Sep. 28, 2005; U.S. Provisional Application Ser. No. 60 / 738,981, filed on Nov. 23, 2005, all of which are hereby incorporated herein by reference in their entireties.FIELD OF THE INVENTION[0002]The present invention relates to the treatment of primary disorders of mood and affect with a neurotoxin, including depressive, anxiety and sleep disorders as well as other CNS disorders.BACKGROUND OF THE INVENTION[0003]Depression is one of the most prevalent and pervasive forms of mental illness that affects individuals across age and gender lines. (Gainotti et al. (2001) J. Neural Neurosurg. Psychiatr. 71: 258-261; Wong et al. (2001) Nature Rev. Neurosci. 2: 343-351; Nestler et al. (2002) Neuron 34: 13-25). The lifetime risk of major depression is...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K38/48A61K49/00
CPCA61K49/0004A61K38/4893A61K9/0019A61K9/0021A61K9/08A61K47/10A61K47/44C12Y304/24069Y02A50/30A61K9/1075A61K2121/00
Inventor BORODIC, GARY E.
Owner REVANCE THERAPEUTICS INC
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