WO2009103150A4 - Method for treating migraine headaches - Google Patents
Method for treating migraine headaches Download PDFInfo
- Publication number
- WO2009103150A4 WO2009103150A4 PCT/CA2009/000182 CA2009000182W WO2009103150A4 WO 2009103150 A4 WO2009103150 A4 WO 2009103150A4 CA 2009000182 W CA2009000182 W CA 2009000182W WO 2009103150 A4 WO2009103150 A4 WO 2009103150A4
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- migraine
- blocking agent
- beta adrenergic
- adrenergic blocking
- solution
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/075—Ethers or acetals
- A61K31/08—Ethers or acetals acyclic, e.g. paraformaldehyde
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
- A61K31/138—Aryloxyalkylamines, e.g. propranolol, tamoxifen, phenoxybenzamine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
- A61K31/382—Heterocyclic compounds having sulfur as a ring hetero atom having six-membered rings, e.g. thioxanthenes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/557—Eicosanoids, e.g. leukotrienes or prostaglandins
- A61K31/5575—Eicosanoids, e.g. leukotrienes or prostaglandins having a cyclopentane, e.g. prostaglandin E2, prostaglandin F2-alpha
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0048—Eye, e.g. artificial tears
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/06—Antimigraine agents
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Ophthalmology & Optometry (AREA)
- Pain & Pain Management (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
A beta adrenergic blocking agent, preferably Timolol maleate, or ocularly compatible salts thereof, are delivered topically in the form of one or more eye drops during the interval beginning from the time and within the first 30 minutes thereafter when a patient first senses the onset, or potential onset, of a migraine headache.
Claims
1. A method for treatment of a person anticipating suffering from a migraine headache comprising topical administration of a therapeutically effective amount of a pharmaceutically acceptable solution of a beta adrenergic blocking agent, or an ocularly compatible salt thereof, in the form of one or more eye drops delivered to one or both eyes within 30 minutes of the first indication of said migraine.
2. The method as in claim 1 wherein the beta adrenergic blocking agent is selected from the group consisting of betoxoloh. levobunolo^ carteololi metipranoloL. levobetaxolol, and timolol.
3. The method as in claim 1 or 2 wherein the solution is administered to both eyes.
4. The method as in any one of claims 1 to 3, wherein the eye drops are administered repeatedly thereafter in a similar manner every half hour for up to two hours in cases where the migraine persists.
5. The method as in any one of claims 1 to 4 comprising administration of an aqueous pharmaceutical solution of Timolol maleate, or ocularly compatible salts thereof, at a concentration of from a 0.25% to 0.5%.
6. The method as in claim 5 wherein the pharmaceutical solution is a 0.5% aqueous solution.
7. Use of a therapeutically effective amount of a beta adrenergic blocking agent or an ocularly compatible salt thereof for treatment of a migraine, wherein said beta adrenergic blocking agent or ocularly compatible salt thereof is for ophthalmic administration within 30 minutes of a first indication of said migraine.
8. The use as in claim 7 wherein the beta adrenergic blocking agent is selected from the group consisting of betoxolol; levobunolol; carteolol; metipranolol; levobetaxolol; and timolol.
9. Use of a beta adrenergic blocking agent or an ocularly compatible salt thereof in the manufacture of an ophthalmic solution for treatment of a migraine, wherein said solution is for ophthalmic administration within 30 minutes of a first indication of said migraine,
10. The use as in claim 9 wherein the beta adrenergic blocking agent is selected from the group consisting of betoxolol; levobunolol; carteolol; metipranolol; levobetaxolol; and timolol.
10 Statement under Article 19 (I) The claims have been amended as follows:
Claim 2 has been amended to recite beta blocking agents in Markush format. Support for this amendment is found at paragraph [0013]. A similar amendment has been made to claims 8 and 10. Claims 3, 5 and 7 have been amended for better clarity.
No new matter has been entered by way of the above amendments.
This statement is accompanied by a letter as required under Section 205(b).
11
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US3013208P | 2008-02-20 | 2008-02-20 | |
US61/030,132 | 2008-02-20 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2009103150A1 WO2009103150A1 (en) | 2009-08-27 |
WO2009103150A4 true WO2009103150A4 (en) | 2009-10-15 |
Family
ID=40985019
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/CA2009/000182 WO2009103150A1 (en) | 2008-02-20 | 2009-02-20 | Method for treating migraine headaches |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2009103150A1 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2017502089A (en) * | 2014-01-10 | 2017-01-19 | マニスティー パートナーズ エルエルシーManistee Partners Llc | Migraine treatment |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5242949A (en) * | 1992-03-13 | 1993-09-07 | Rugby-Darby Group Companies, Inc. | Treating classic migraine |
US5543434A (en) * | 1994-02-25 | 1996-08-06 | Weg; Stuart L. | Nasal administration of ketamine to manage pain |
US5891885A (en) * | 1996-10-09 | 1999-04-06 | Algos Pharmaceutical Corporation | Method for treating migraine |
US6685951B2 (en) * | 2001-07-05 | 2004-02-03 | R. T. Alamo Ventures I, Inc. | Administration of dihydroergotamine as a sublingual spray or aerosol for the treatment of migraine |
IL147921A0 (en) * | 2002-01-31 | 2002-08-14 | Abdulrazik Mohammad | A method for treating central nervous system disorders by ocular dosing |
-
2009
- 2009-02-20 WO PCT/CA2009/000182 patent/WO2009103150A1/en active Application Filing
Also Published As
Publication number | Publication date |
---|---|
WO2009103150A1 (en) | 2009-08-27 |
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