AU2007202484B2 - Method for treating pain associated with a muscle disorder - Google Patents

Description

Our Ref:20226399 P/00/0 I I Regulation 3:2 AUSTRALIA Patents Act 1990 ORIGINAL COMPLETE SPECIFICATION STANDARD PATENT Applicant(s): Allergan, Inc. 2525 Dupont Drive Irvine California 92612 United States of America Address for Service: DAVIES COLLISON CAVE Patent & Trade Mark Attorneys 255 Elizabeth Street Sydney, New South Wales, Australia, 2000 Invention Title: Method for treating pain associated with a muscle disorder The following statement is a full description of this invention, including the best method of performing it known to me:- METHOD FOR TREATING PAIN ASSOCIATED WITH A MUSCLE DISORDER FIELD OF THE fNVENTION 5 The present invention provides novel methods for treating various disorders and conditions, with Botulinum toxins. Importantly, the present invention provides methods useful in relieving pain related to muscle activity or contracture and therefore is of advantage in the treatment of, for example, muscle spasm such as 10 Temporomandibular Joint Disease, low back pain, myofascial pain, pain related to spasticity and dystonia, as well as sports injuries, and pain related to contractures in arthritis. The invention also provides compositions suitable for use in the methods. BACKGROUND OF THE INVENTION 15 Heretofore, Botulinum toxins, in particular Botulinum toxin type A, has been used in the treatment of a number of neuromuscular disorders and conditions involving muscular spasm; for example, strabismus, blepharospasm, spasmodic torticollis (cervical dystonia), oromandibular dystonia and spasmodic dysphonia 20 (laryngeal dystonia). The toxin binds rapidly and strongly to presynaptic cholinergic nerve terminals and inhibits the exocytosis of acetylcholine by decreasing the frequency of acetylcholine release. This results in local paralysis and hence relaxation of the muscle afflicted by spasm. 25 For one example of treating neuromuscular disorders, see U.S. Patent No. 5,053,005 to Borodic, which suggests treating curvature of the juvenile -2 spine, i.e., scoliosis, with an acetylcholine release inhibitor, preferably Botulinum toxin A. For the treatment of strabismus with Botulinum 5 toxin type A, see Elston, J.S., et al., British Journal of Ophthalmology, 1985, 69, 718-724 and 891 896. For the treatment of blepharospasm with Botulinum toxin type A, see Adenis, J.P., et al., J. Fr. Ophthalmol-, 1990, 13 (5) at pages 259-264. 10 For treating squint, see Elston, J.S., Eye, 1990, 4(4):VII. For treating spasmodic and oromandibular dystonia torticollis, see Jankovic et al. , Neurology, 1987, 37, 616-623. 15 Spasmodic dysphonia has been treated with Botulinum toxin type A. See Blitzer et al., Ann. Otol. Rhino. Laryngol, 1985, 94, 591-594. Lingual dystonia was treated with Botulinum toxin type A according to Brin et al., Adv. Neurol. (1987) 50, 599 20 608. Finally, Cohen et al., Neurology (1987) 37 (Suppl. 1), 123-4, discloses the treatment of writer's cramp with Botulinum toxin type A. The term Botulinum toxin is a generic term 25 embracing the family of toxins produced by the anae robic bacterium Clostridium botulinum and, to date, seven immunologically distinct neurotoxins have been identified. These have been given the designations A, B, C, D, E, F and G. For further information con 30 cerning the properties of the various Botulinum toxins, reference is made to the article by Jankovic and Brin, The New England Journal of Medicine, No. 17, 1990, pp. 1186-1194, and to the review by Charles L. Hatheway in Chapter 1 of the book entitled Botulinun 35 Neurotoxin and Tetanus Toxin, L. L. Simpson, Ed., -3 published by Academic Press Inc. of San Diego, California, 1989, the disclosures in which are incorporated herein by reference. 5 The neurotoxic component of Botulinum toxin has a molecular weight of about 150 kilodaltons and is thought to comprise a short polypeptide chain of about 50 kD which is considered to be responsible for the toxic properties of the toxin, i.e., by interfering 10 with the exocytosis of acetylcholine, by decreasing the frequency of acetylcholine release, and a larger polypeptide chain of about 100 kD which is believed to be necessary to enable the toxin to bind to the pre synaptic membrane. 15 The "short" and "long" chains are linked together by means of a simple disulfide bridge. (It is noted that certain serotypes of Botulinum toxin, e.g., type E, may exist in the form of a single chain un-nicked 20 protein, as opposed to a dichain. The single chain form is less active but may be converted to the corresponding dichain by nicking with a protease, e.g., trypsin. Both the single and the dichain are useful in the method of the present invention.) 25 In general, four physiologic groups of C. botuli num are recognized (I, II, III, IV). The organisms capable of producing a serologically distinct toxin may come from more than one physiological group. For 30 example, Type B and F toxins can be produced by strains from Group I or II. In addition, other strains of clostridial species (C. baratii, type F; C. butyricum, type E; C. novyi, type C 1 or D) have been identified which can produce botulinum 35 neurotoxins.

P %WPDOCS\CRN\XSpec\2O226399 spec doc.2205/2(009 -4 Immunotoxin conjugates of ricin and antibodies, which are characterized as having enhanced cytotoxicity through improving cell surface affinity, are disclosed in European Patent Specification 0 129 434. The inventors note that botulinum toxin may be utilized in place of ricin. 5 Botulinum toxin is obtained commercially by establishing and growing cultures of C. botulinum in a fermenter and then harvesting and purifying the fermented mixture in accordance with known techniques. 10 Botulinum toxin type A, the toxin type generally utilized in treating neuromuscular conditions, is currently available commercially from several sources; for example, from Porton Products Ltd. UK, under the trade name "DYSPORT," and from Allergan, Inc., Irvine, California, under the trade name BOTOX*. 15 The invention provides novel treatments of neuromuscular disorders and conditions with various Botulinum toxin types. The present invention also seeks to relieve pain with various Botulinum toxin types. SUMMARY OF THE INVENTION 20 A first aspect of the invention provides a method for treating spasticity pain, the method comprising the step of administering to a human patient a therapeutically effective amount of the neurotoxic component from a single serotype of a botulinum toxin, to thereby treat the spasticity pain, wherein the neurotoxic component administered to the 25 patient has been purified from a botulinum toxin obtained by fermenting Clostridium botulinum. A second aspect of the invention provides a method for treating spasticity pain, the method comprising the step of administering to a patient a therapeutically effective amount 30 of the neurotoxic component of only a botulinum toxin type A to thereby treat the spasticity pain, wherein the neurotoxic component administered to the patient has been P \WPDOC5\CRN\jX\Spec2O226399 spec doc.22M5/2009 - 4a purified from a botulinum toxin obtained by fermenting a Clostridium botulinum bacterium. A third aspect of the invention provides a method for treating pain associated with 5 post-stroke spasticity, the method comprising the step of administering to a patient a therapeutically effective amount of the neurotoxic component of only a botulinum toxin type A to thereby treat the pain associated with post-stroke spasticity, wherein the neurotoxic component administered to the patient has been purified from a botulinum toxin type A obtained by fermenting a Clostridium botulinum bacterium. 10 A fourth aspect of the invention provides a use of the neurotoxic component from a single serotype of a botulinum toxin, wherein the neurotoxic component has been purified from a botulinum toxin obtained by fermenting Clostridium botulinum, in the manufacture of a medicament for treating spasticity pain. 15 A fifth aspect of the invention provides a use of the neurotoxic component of only a botulinum toxin type A, wherein the neurotoxic component has been purified from a botulinum toxin type A obtained by fermenting a Clostridium botulinum bacterium, in the manufacture of a medicament for treating spasticity pain. 20 A sixth aspect of the invention provides a use of the neurotoxic component of only a botulinum toxin type A, wherein the neurotoxic component has been purified from a botulinum toxin type A obtained by fermenting a Clostridium botulinum bacterium, in the manufacture of a medicament for treating pain associated with post-stroke spasticity. 25 30 -5 The present invention provides a method for relieving pain, associated with muscle contractions, a composition and a method of treating conditions such as cholinergic 'ontrolled secretions including excessive sweating, lacrimation and 5 mucus secretions and a method for treating smooth muscle disorders including, but not limited to, spasms in the sphincter of the cardiovascular arteriole, gastrointestinal system, urinary, gall bladder and rectum, which method comprises administering to the patient suffering from said disorder or condition a therapeutically effective amount of Botulinum toxin selected from the group consisting of Botulinum toxin 10 types B, C, D, E, F and G. Each serotype of Botulinum toxin has been identified as immunologically different proteins through the use of specific antibodies. For example, if the antibody (antitoxin) recognises, that is, neutralises the biological activity of , for 15 example, type A it will not recognise types B, C, D, E, F or G. While all of the Botulinum toxins appear to be zinc endopeptidases, the mechanism of action of different serotypes, for example, A and E within the neuron appear to be different than that of Type B. In addition, the neuronal surface 20 "receptor" for the toxin appears to be different for the serotypes. In the area of use of the Botulinum toxins in accordance with the present invention with regard to organ systems which involve the release of neurotransmitter, it is expected to introduce the toxins A, B, C, D, E, F, and G 25 directly by local injections. Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated integer or step or 30 group of integers or steps but not the exclusion of any other integer or step or group of integers or steps. DETAILED DESCRIPTION 35 The Botulinum toxins used according to the present invention are Botulinum toxins type A, B, C, D, E, F and G.

-6 The physiologic groups of Clostridium botulinum types are listed in Table I. Table I. Physiologic Groups or Closoidium botuhnurn Toi" GIuen3se PbFhage P a*zo y 5 Grup Scro- Diochcaisty pk OrZc e & Retaicd Type Digestztnic (0o0taigenic) I A.B.F proteolytic saccharolytic + + + + C. spo rnes 11 B.E.F nonprocolyic saccharolnyic psychotrophic - + + + IlIl C.D nonproteolytic saccharolytic + + + + C novy IV G protcolyic "*"''"e''"'l'i' + - - . C suiermnak 10 These toxin types may be produced by selection from the appropriate physiologic group of Clostridiun botulinum organisms, the organisms designated as Group I are usually referred to as proteolytic and 15 produce Botulinum toxins of types A, B and F. The organisms designated as Group II are saccharolytic and produce Botulinum toxins of types B, E and F. The organisms designated as Group III produce only Botulinum toxin types C and D and are distinguished 20 from organisms of Groups I and II by the production of significant amounts of propionic acid. Group IV organisms only produce neurotoxin of type G. The production of any and all of the Botulinum toxin types A, B, C, D, E, F and G are described in Chapter 1 of 25 Botulinum Neurotoxin and Tetanus Toxin, cited above, and/or the references cited therein. Botulinum toxins types B, C, D, E, F and G are also available from various species of clostridia. 30 Currently fourteen species of clostridia are considered pathogenic. Most of the pathogenic strains produce toxins which are responsible for the various pathological signs and symptoms. organisms which pro- -7 duce Botulinum toxins have been isolated from botulism outbreaks in humans (types A, B, E and F) and animals (types C and D). Their identities were described through the use of specific antitoxins (antibodies) 5 developed against the earlier toxins. Type G toxin was found in soil and has low toxigenicity. However, it has been isolated from autopsy specimens, but thus far there has not been adequate evidence that type G botulism has occurred in humans. 10 Preferably, the toxin is administered by means of intramuscular injection directly into a local. area such as a spastic muscle, preferably in the region of the neuromuscular junction, although alternative types 15 of administration (e.g., subcutaneous injection), which can deliver the toxin directly to the affected region, may be employed where appropriate. The toxin can be presented as a sterile pyrogen-free aqueous solution or dispersion and as a sterile powder for 20 reconstitution into a sterile solution or dispersion. Where desired, tonicity adjusting agents such as sodium chloride, glycerol and various sugars can be added. Stabilizers such as human serum albumin may 25 also be included. The formulation may be preserved by means of a suitable pharmaceutically acceptable pre servative such as a paraben, although preferably it is unpreserved. 30 It is preferred that the toxin is formulated in unit dsfrm:; for exA-al-ample, it can be provided as a sterile solution in a vial or as a vial or sachet containing a lyophilized powder for reconstituting a suitable vehicle such as saline for injection. 35 r -8 In one embodiment, the Botulinum toxin is formulated in a solution containing saline and pas teurized human serum albumin, which stabilizes the toxin and minimizes loss through non-specific adsorp 5 tion. The solution is sterile filtered (0.2 micron filter), filled into individual vials and then vacuum dried to give a sterile lyophilized powder. In use, the powder can be reconstituted by the addition of sterile unpreserved normal saline (sodium chloride 10 0.9% for injection). The dose of toxin administered to the patient will depend upon the severity of the condition; e.g., the number of muscle groups requiring treatment, the 15 age and size of the patient and the potency of -the toxin. The potency of the toxin is expressed as a multiple of the LDSo value for the mouse, one unit (U) of toxin being defined as being the equivalent to that amount, on a per mouse basis, that kills 50% of a group of Swiss-Webster mice weighing between 17 20 and 22 grams each. The dosages used in human therapeutic applications are roughly proportional to the mass of muscle being injected. Typically, the dose admin 25 istered to the patient may be up from about. 0.01 to about 1,000 units; for example, up to about 500 units, and preferably in the range from about 80 to about 460 units per patient per treatment, although smaller of larger doses may be administered in appropriate cir 30 cumstances such as up to about 50 units for the relief of pain and in controlling cholinergic secretions. As the physicians become more familiar with the use of this product, the dose may be changed. In the 35 Botulinum toxin type A, available from Porton, -9-. DYSPORT, 1 nanogram (ng) contains 40 units. 1 ng of the Botulinum toxin type A, available from Allergan, Inc., i.e., BOTOX*, contains 4 units. The potency of Botulinum toxin and its long duration of action mean 5 that doses will tend to be administered on an infrequent basis. Ultimately, however, both the quantity of toxin administered and the frequency of its administration will be at the discretion of the physician responsible for the treatment and will be, 10 commensurate with questions of safety and the effects produced by the toxin. In some circumstances, particularly in the relief of pain associated with sports injuries, such as, for 15 example, charleyhorse, botulinum type F, having a short duration activity, is preferred. The invention will now be illustrated by reference to the following nonlimiting examples. 20 In each of the examples, appropriate areas of each patient are injected with a sterile solution con taining the confirmation of Botulinum toxin. Total patient doses range from about 0.01 units to 460 25 units. Before injecting any muscle group, careful consideration is given to the anatomy of the muscle group, the aim being to inject the area with the highest concentration of neuromuscular junctions, if known. Before injecting the muscle, the position of 30 the needle in the muscle is confirmed by putting the muscle through its range Of motion and observing the resultant motion of the needle end. General anaesthesia, local anaesthesia and sedation are used according to the age of the patient, the number of 35 sites to be injected, and the particular needs of the -10 patient. More than one injection and/or sites of injection may be necessary to achieve the desired result. Also, some injections, depending on the muscle to be injected, may require the use of fine, 5 hollow, teflon-coated needles, guided by electromyography. Following injection, it is noted that there are no systemic or local side effects and none of the 10 patients are found to develop extensive local hypoton icity. The majority of patients show an improvement in function both subjectively and when measured objectively. 15 Example I The Use of Botulinum toxin Type in the Treatment of Tardive Dyskinesia A male patient, age 45, suffering from tardive 20 dyskinesia resulting from the treatment with an antipsychotic drug, such as Thorazine or Haldol, is treated with 150 units of Botulinum toxin type B by direct injection of such toxin into the facial muscles. After 1-3 days, the symptoms of tardive 25 dyskinesia, i.e., orofacial dyskinesia, athetosis, dystonia, chorea, tics and facial grimacing, etc. are markedly reduced. Example 1(a) 30 The method of Example I is repeated, except that a patient suffering from tardive dyskinesia is injected with 50-200 units of Botulinum toxin type C. A similar result is obtained. 35 -11 Example l(b) The method of Example 1 is repeated, except that a patient suffering from tardive dyskinesia is 5 injected with 50-200 units of Botulinum toxin type D:. A similar result is obtained. Example 1(c) 10 The method of Example 1 is repeated, except that a patient suffering from tardive dyskinesia is injected with 50-200 units of Botulinum toxin type E. A similar result is obtained. 15 Example I(d) The method of Example 1 is repeated, except that a patient suffering from tardive dyskinesia is injected with 50-200 units of Botulinum toxin type F. 20 A similar result is obtained. Example I(e) The method of Example I is repeated, except that 25 a patient suffering from tardive dyskinesia is injected with 50-200 units of Botulinum toxin type G. A similar result is obtained. Example 2 30 The Use of Botulinum toxin Type B in the Treatment of SpasmOdic Torticolli 5 A male, age 45, suffering from spasmodic torticollis, as manifested by spasmodic or tonic 35 contractions of the neck musculature, producing -12 stereotyped abnormal deviations of the head, the chin being rotated to one side, and the shoulder being elevated toward the side at which the head is rotated, is treated by injection with 100-1,000 units of 5 Botulinum toxin type E. After 3-7 days, the symptoms. are substantially alleviated; i.e., the patient is able to hold his head and shoulder in a normal position. 10 Example 2 (a) The method of Example 2 is repeated, except that a patient suffering from spasmodic torticollis is injected with 100-1,000 units of Botulinum toxin type 15 B. A similar result is obtained. Example 2(b) The method of Example 2 is repeated, except that 20 a patient suffering from spasmodic torticollis is injected with 100-1,000 units of Botulinum toxin type C. A similar result is obtained. Example 2(c) 25 The method of Example 2 is repeated, except that a patient suffering from spasmodic torticollis is injected with 100-1,000 units of Botulinum toxin type D. A similar result is obtained. 30 Example 2(d) The method of Example 2 is repeated, except that a patient suffering from spasmodic torticollis is -13 injected with 100-1,000 units of Botulinum toxin type E. A similar result is obtained. 5 Example 2(e) The method of Example 2 is repeated, except that a patient suffering from spasmodic torticollis is injected with 100-1,000 units of Botulinum toxin type 10 F. A similar result is obtained. Example 2(f) The method of Example 2 is repeated, except that 15 a patient suffering from spasmodic torticollis is injected with 100-1,000 units of Botulinum toxin type G. A similar result is obtained. 20 Example 3 The Use of Botulinum toxin in the Treatment of Essential Tremor A male, age 45, suffering from essential tremor, 25 which is manifested as a rhythmical oscillation of head or hand muscles and is provoked by maintenance of posture or movement, is treated by injection with 50 1,000 units of Botulinum toxin type B. After two to eight weeks, the symptoms are substantially 30 alleviated; i.e., the patient's head or hand ceases to oscillate.

-14 Example 3(a) The method of Example 3 is repeated, except that a patient suffering from essential tremor is injected 5 with 100-1,000 units of Botulinum toxin type C. A. similar result is obtained. Example 3(b) 10 The method of Example 3 is repeated, except that a patient suffering from essential tremor is injected with 100-1,000 units of Botulinum toxin type D. A similar result is obtained. .15 Example 3(c) The method of Example 3 is repeated, except that a patient suffering from essential tremor is injected with 100-1,000 units of Botulinum toxin type E. A 20 similar result is obtained. Example 3 (d) The method of Example 3 is repeated, except that 25 a patient suffering from essential tremor is injected with 100-1,000 units of Botulinum toxin type F. A similar result is obtained. Example 3(e) 30 The method of Example 3 is repeated, except that a patient suffering from essential tremor is injected with 100-1,000 units of Botulinum toxin type G. A similar result is obtained. 35 -15 Example 4 The Use of Botulinum toxin in the Treatment of Spasmodic Dysphonia 5 A male, age 45, unable to speak clearly, due to spasm of the vocal chords, is treated by injection of the vocal chords with Botulinum toxin type B, having an activity of 80-500 units. After 3-7 days, the patient is able to speak clearly. 10 Example 4(a) The method of Example 4 is repeated, except that a patient suffering from spasmodic dysphonia is 15 injected with 80-500 units of Botulinum toxin type C. A similar result is obtained. Example 4(b) 20 The method of Example 4 is repeated, except that a patient suffering from spasmodic dysphonia is injected with 80-500 units of Botulinum toxin type D. A similar result is obtained. 25 Example 4(c) The method of Example 4 is repeated, except that a patient suffering from spasmodic dysphonia is injected with 80-500 units of Botulinum toxin type E. 30 A similar result is obtained. Example 4(d) The method of Example 4 is repeated, except that 35 a patient suffering from spasmodic dysphonia is -16 injected with 80-500 units of Botulinum toxin type F. A similar result is obtained. Example 4(e) 5 The method of Example 4 is repeated, except that a patient suffering from spasmodic dysphonia is injected with 8-500 units of Botulinum toxin type G. A similar result is obtained. 10 Example 5 The Use of Botulinum toxin Types A-G in the Treatment of Excessive Sweating, Lacrimation or Mucus Secretion or Other Cholinergic Controlled 15 Secretions A male, age 65, with excessive unilateral sweating is treated by administering 0.01 to 50 units, of Botulinum toxin, depending upon degree of desired 20 effect. The larger the dose, usually the greater spread and duration of effect. Small doses are used initially. Any serotype toxin alone or in combination could be used in this indication. The administration is to the gland nerve plexus, ganglion, spinal cord or 25 central nervous system to be determined by the physician's knowledge of the anatomy and physiology of the target glands and secretary cells. In addition, the appropriate spinal cord level or brain area can be injected with the toxin (although this would cause 30 many effects, including general weakness). Thus, the giand (if accessible) or the nerve plexus or ganglion are the targets of choice. Excessive sweating, tearing (lacrimation), mucus secretion or gastrointestinal secretions are positively influenced 35 by the cholinergic nervous system. Sweating and -17 tearing are under greater cholinergic control than mucus or gastric secretion and would respond better to toxin treatment- However, mucus and gastric secretions could be modulated through the cholinergic 5 system. All symptoms would be reduced or eliminated with toxin therapy in about 1-7 days. Duration would be weeks to several months. Example 6 10 The Use of Botulin toxin Tpes A-C in the Treatment of Muscle Spasms in Smooth Muscle Disorders Such AEs Sphincters of the cardiovascular Arterioler Gastrointestinal System. Urinary or Gall Bladder, Rectal, Etc. .15 A male, age 30-40, with a constricted pyloric valve which prevents his stomach from emptying, is treated by administering 1-50 units of Botulinun toxin. The administration is to the pyloric valve 20 (which controls release of stomach contents into the intestine) divided into 2 to 4 quadrants, injections made with any endoscopic device or during surgery. In about 1-7 days, normal emptying of the stomach, elimination or drastic reduction in regurgitation 25 occurs. Example 7 The Use of Botulinum toxin Types A-G in the Treatment of Muscle Spasms and control of Pain 30 Associated with Muscle Spasms in Temporal Mandibular Joint Disorders A female, age 35, is treated by administration of 0.1 to 50 units total of Botulinum toxin. The 35 administration is to the muscles controlling the -18 closure of the jaw. Overactive muscles may be identified with EMG electromyographyy) guidance. Relief of pain associated with muscle spasms, possible reduction in jaw clenching occurs in about 1-3 days. 5 Example 8 The Use of Botulinum toxin Types A-G in the Treatment of Muscle Spasms and Control of Pain Associated with Muscle Spasms in Conditions 10 Secondary to Sports Injuries (Charleyhorse) A male, age 20, with severe cramping in thigh after sports injury is treated by administration of a short duration toxin, possible low dose (0.1-25 units) 15 of preferably type F to the muscle and neighboring muscles which are in contraction ("cramped"). Relief of pain occurs in 1-7 days. Example 9 20 The Use of Botulinun toxin Types A-G in the Treatment of Muscle Spasms and Control of Pain Associated with Muscle Spasms in Smooth Muscle Disorders Such as Gastrointestinal Muscles 25 A female, age 35, with spastic colitis, is treated with 1-100 units of Botulinum toxin divided into several areas, enema (1-5 units) delivered in the standard enema volume, titrate dose, starting with the lowest dose. Injection is to the rectum or lower 30 colon or a low dose enema may be employed- Cramps and pain associated with spastic colon are relieved in 1-10 days.

-19 Example 10 The Use of Botulinum toxin Types A-G in the Treatment of Muscle Spasms and Control of Pain Associated with Muscle Spasms in Spasticity 5 Conditions Secondary to Stroke. Traumatic Brain or Spinal Cord Iniury A male, age 70, post-stroke or cerebral vascular event, is injected with 50 to 300 units of Botulinum 10 toxin in the major muscles involved in severe closing of hand and curling of wrist and forearm or the muscles involved in the closing of the legs such that the patient and attendant have difficulty with hygiene. Relief of these symptoms occurs in 7 to 21 .15 days. Example 11 The Use of Botulinum toxin Types A-G in the Treatment of Patients with Swallowing disorders 20 A patient with a swallowing disorder caused by excessive throat muscle spasms is injected with about 1 to about 300 units of Botulinum toxin in the throat muscles. Relief the swallowing disorder occurs in 25 about 7 to about 21 days.

-20 Exarnple 12 The Use of Botulinum toxin Types A-G in the Treatment of Patients with Tension Headache 5 A patient with a tension headache caused by excessive throat muscle spasms is injected with about 1 to about 300 units of Botulinum toxin in muscles of the head and upper neck. Relief of the tension headache occurs in about 1 to about 7 days. 10 Although there has been hereinabove described a use of Botulinum toxins for treating various dis orders, conditions and pain, in accordance with the present invention, for the purpose of illustrating the 15 manner in which the invention may be used to advan tage, it should be appreciated that the invention is not limited thereto since many obvious modifications can be made, and it is intended to include within this invention any such modifications as will fall within 20 the scope of the appended claims. Accordingly, any and all modifications, variations, or eq-uivalent arrangements which may occur to those skilled in the art, should be considered to be within the scope of the present invention as defined in the appended 25 claims. The reference to any prior art in this specification is not, and should not be taken as, an acknowledgment or any form of suggestion that that prior art forms part of the common general knowledge in Australia.

Claims (19)

1. A method for treating spasticity pain, the method comprising the step of administering to a human patient a therapeutically effective amount of the 5 neurotoxic component from a single serotype of a botulinum toxin, to thereby treat the spasticity pain, wherein the neurotoxic component administered to the patient has been purified from a botulinum toxin obtained by fermenting Clostridium botulinum. 10

2. The method of claim 1, wherein the single botulinum toxin serotype, from which the neurotoxic component administered is purified, is selected from the group consisting of botulinum toxin types A, B, C, D, E, F and G.

3. The method of claim 1, wherein the botulinum toxin is botulinum toxin type A. 15

4. The method of any one of claims 1 to 3, wherein between about I unit and about 250 units of the neurotoxic component of the botulinum toxin is administered.

5. The method of any one of claims 1 to 4, wherein the neurotoxic component has a 20 molecular weight of about 150 kilodaltons.

6. The method of any one of claims I to 5, wherein the spasticity is associated with post-stroke spasticity. 25

7. The method of any one of claims I to 5, wherein the spasticity is secondary to a brain injury, or a spinal cord injury.

8. The method of any one of claims 1 to 7, wherein the neurotoxic component is administered by local administration. 30 P:WPDOCSCRNUXJSpc2O226399 pe do.22/5/209 - 22

9. A method for treating spasticity pain, the method comprising the step of administering to a patient a therapeutically effective amount of the neurotoxic component of only a botulinum toxin type A to thereby treat the spasticity pain, wherein the neurotoxic component administered to the patient has been purified 5 from a botulinum toxin obtained by fermenting a Clostridium botulinum bacterium.

10. The method of claim 9, wherein the neurotoxic component has a molecular weight of about 150 kilodaltons. 10

11. The method of claim 9 or claim 10, wherein the spasticity is associated with post stroke spasticity.

12. The method of claim 9 or claim 10, wherein the spasticity is secondary to a brain injury or a spinal cord injury. 15

13. A method for treating pain associated with post-stroke spasticity, the method comprising the step of administering to a patient a therapeutically effective amount of the neurotoxic component of only a botulinum toxin type A to thereby treat the pain associated with post-stroke spasticity, wherein the neurotoxic component 20 administered to the patient has been purified from a botulinum toxin type A obtained by fermenting a Closiridium botulinum bacterium.

14. The method of claim 13, wherein the neurotoxic component has a molecular weight of about 150 kilodaltons. 25

15. The method of claim 13 or claim 14, wherein the neurotoxic component is administered by local administration.

16. Use of the neurotoxic component from a single serotype of a botulinum toxin, 30 wherein the neurotoxic component has been purified from a botulinum toxin obtained by fermenting Clostridium botulinum, in the manufacture of a medicament P.WPDOCS\CRNUXJ\Spec\2226399 speLoc-22/05/2009 - 23

17. Use of the neurotoxic component of only a botulinum toxin type A, wherein the neurotoxic component has been purified from a botulinum toxin type A obtained by fermenting a Clostridium botulinum bacterium, in the manufacture of a medicament for treating spasticity pain. 5

18. Use of the neurotoxic component of only a botulinum toxin type A, wherein the neurotoxic component has been purified from a botulinum toxin type A obtained by fermenting a Clostridium botulinum bacterium, in the manufacture of a medicament for treating pain associated with post-stroke spasticity. 10

19. A method for treating spasticity pain according to any one of claims 1, 9 or 13, substantially as hereinbefore described with reference to the Examples.