Topical therapy for the treatment of migraines, muscle sprains, muscle spasms, spasticity and related conditions
The invention is directed to topical formulations and methods of treating a migraines and/or cluster headaches, muscle sprains, muscle spasms, spasticity, tension headaches, tension related migraines and related conditions associated with muscle tension and pain with a therapeutically effective amount of an ergot alkaloid, skeletal muscle relaxant, serotonin agonist, combinations thereof, pharmaceutically acceptable salt thereof, prodrugs thereof or derivative thereof.
1. A method of treating migraines and cluster headaches with a topical formulation comprising applying a unit dose of a therapeutically effective amount of the active agent tizanidine or a pharmaceutically acceptable salt thereof incorporated into an immediate release pharmaceutically acceptable topical carrier onto the skin of a human patient experiencing an acute condition selected from the group consisting of migraine and cluster headache, at the posterior cervical area in close proximity to the brain stem, such that the unit dose provides a therapeutic effect within about 15 to about 30 minutes after topical administration to the human patient.
2. The method of claim 1 , wherein the formulation further comprises a therapeutically effective amount of a serotonin agonist.
3. The method of claim 1 , wherein the topical carrier is an aqueous based carrier.
4. The method of claim 1 , wherein the topical formulation in a form selected from the group consisting of a liquid, a semisolid, a solid and mixtures thereof.
5. The method of claim 1 , further comprising incorporating a therapeutic amount of the active agent into the unit dose such that the active agent would provide a subtherapeutic plasma level if orally administered, but is therapeutically effective when administered topically at the posterior cervical area.
6. The method of claim 1 , wherein the unit dose further comprises a therapeutically effective amount of an ergot alkaloid selected from the group consisting of bromocriptine, ergocristine, ergocristinine, ergotamine, ergotaminine, ergocryptine, ergocryptinine, ergocornine, ergocorninine, ergosine, ergosinine, ergonovine, ergometrinine, dihydroergotamine, lisuride, d-lysergic acid, d-isolysergic acid, lysergol, lergotrile, metergoline, methysergide, methylergonovine, pharmaceutically acceptable salts thereof, and mixtures thereof.
7. The method of claim 6 , wherein the ergot alkaloid is selected from the group consisting of dihydroergotamine base, dihydroergotamine mesylate, and mixtures thereof.
8. The method of claim 6 , wherein the therapeutically effective amount of ergot alkaloid ranges from about 0.1 mg to about 10 mg, preferably from about 0.5 mg to about 6 mg.
9. The method of claim 1 , wherein the unit dose comprises from about 0.2 mg to about 8 mg of tizanidine hydrochloride.
10. The method of claim 2 , wherein the serotonin agonist is selected from the group consisting of sumatriptan, naratriptan, eletriptan, rizatriptan, zolmitriptan, almotriptan, frovatriptan, pharmaceutically acceptable salts thereof, and mixtures thereof.
11. The method of claim 10 , wherein the serotonin agonist is sumatriptan.
12. The method of claim 11 , wherein the unit dose comprises from about 0.5 mg to about 200 mg sumatriptan.
13. The method of claim 11 , wherein the unit dose comprises from about 5 mg to about 50 mg sumatriptan.
14. The method of claim 1 , further comprising incorporating one or more ingredients into the topical formulation selected from the group consisting of ethoxydiglycol, water, glycerine, C12-15alkyl benzoate, glyceryl stearate, dimethicone, cetearyl alcohol, cetearyl glucoside, polyacrylamide, cetyl alcohol, magnesium aluminum silicate, xanthan gum, aloe vera (aloe barbadensis), tocopheryl acetate (vitamin E acetate), prunus amygadalus amara (bitter almond) kernel oil, vitis vinifera (grape) seed extract, triticum vulgare (wheat) germ oil, retinyl palmitate (vitamin A palmitate), ascorbyl palmitate (vitamin C palmitate), pro-lipo multi-emulsion liposomic system, tetrasodium EDTA, phenoxyethanol, and sodium hydroxymethylglycinate.
15. The method of claim 1 , wherein the unit dose comprises from about 0.2 mg to about 4 mg of tizanidine hydrochloride.
16. A method of treating migraines and cluster headaches with a topical formulation comprising applying a unit dose of from about 0.2 mg to about 8 mg of tizanidine hydrochloride and from about 0.5 mg to about 200 mg sumatriptan succinate, incorporated into a pharmaceutically acceptable carrier, onto the skin of a human patient experiencing an acute condition selected from the group consisting of migraine and cluster headache, at the posterior cervical area in close proximity to the brain stem of the human patient, such that the unit dose provides a therapeutic effect within about 15 to about 30 minutes after topical administration to the human patient.
17. The method of claim 16 , wherein the unit dose comprises from about 0.4 mg to 4 mg of tizanidine hydrochloride and from about 5 mg to 50 mg sumatriptan succinate.
18. The method of claim 16 , further comprising applying an additional unit dose onto the skin of the human patient at the posterior cervical area from about 15 minutes to about 3 hours after the first application of the unit dose.
19. The method of claim 16 , wherein the topical formulation further comprises from about 0.1 mg to about 10 mg of an ergot alkaloid.
20. The method of claim 16 , wherein the pharmaceutical acceptable carrier is aqueous-based.