UA76399C2 - Use of eletriptan for prevention of migraine recurrence - Google Patents

Use of eletriptan for prevention of migraine recurrence Download PDF

Info

Publication number: UA76399C2
Authority: UA; Ukraine
Prior art keywords: eletriptan; pharmaceutically acceptable; salt; migraine; release
Prior art date: 1998-07-30

Application number

UA2001010653A

Other languages

English (en)

Ukrainian (uk)

Inventor

Neville Colin Jackson

Original Assignee

Pfizer

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1998-07-30

Filing date

1999-06-14

Publication date

2006-08-15

1999-06-14 Application filed by Pfizer filed Critical Pfizer

2006-08-15 Publication of UA76399C2 publication Critical patent/UA76399C2/uk

Links

208000019695 Migraine disease Diseases 0.000 title claims abstract description 57
206010027599 migraine Diseases 0.000 title claims abstract description 57
OTLDLQZJRFYOJR-LJQANCHMSA-N eletriptan Chemical compound CN1CCC[C@@H]1CC1=CN=C2[C]1C=C(CCS(=O)(=O)C=1C=CC=CC=1)C=C2 OTLDLQZJRFYOJR-LJQANCHMSA-N 0.000 title claims abstract description 50
229960002472 eletriptan Drugs 0.000 title claims abstract description 49
230000002265 prevention Effects 0.000 title abstract description 8
150000003839 salts Chemical class 0.000 claims abstract description 57
239000000203 mixture Substances 0.000 claims abstract description 33
239000003814 drug Substances 0.000 claims abstract description 8
238000004519 manufacturing process Methods 0.000 claims abstract description 6
238000000034 method Methods 0.000 claims description 11
230000002035 prolonged effect Effects 0.000 claims description 11
230000003111 delayed effect Effects 0.000 claims description 10
230000000541 pulsatile effect Effects 0.000 claims description 9
RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 claims description 8
229940126601 medicinal product Drugs 0.000 claims description 8
229940079593 drug Drugs 0.000 claims description 7
230000001105 regulatory effect Effects 0.000 claims description 6
CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical group Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims description 4
LPHGQDQBBGAPDZ-UHFFFAOYSA-N Isocaffeine Natural products CN1C(=O)N(C)C(=O)C2=C1N(C)C=N2 LPHGQDQBBGAPDZ-UHFFFAOYSA-N 0.000 claims description 4
229960001948 caffeine Drugs 0.000 claims description 4
VJEONQKOZGKCAK-UHFFFAOYSA-N caffeine Natural products CN1C(=O)N(C)C(=O)C2=C1C=CN2C VJEONQKOZGKCAK-UHFFFAOYSA-N 0.000 claims description 4
229920000858 Cyclodextrin Polymers 0.000 claims description 3
IYVZCNNIKYUHHM-WXMGBDCWSA-N OS(O)(=O)=O.CN1CCC[C@@H]1CC(C1=C2)=CNC1=CC=C2CCS(=O)(=O)C1=CC=CC=C1.CN1CCC[C@@H]1CC(C1=C2)=CNC1=CC=C2CCS(=O)(=O)C1=CC=CC=C1 Chemical compound OS(O)(=O)=O.CN1CCC[C@@H]1CC(C1=C2)=CNC1=CC=C2CCS(=O)(=O)C1=CC=CC=C1.CN1CCC[C@@H]1CC(C1=C2)=CNC1=CC=C2CCS(=O)(=O)C1=CC=CC=C1 IYVZCNNIKYUHHM-WXMGBDCWSA-N 0.000 claims description 3
HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 claims description 3
238000002360 preparation method Methods 0.000 claims description 2
238000012876 topography Methods 0.000 claims 1
239000008194 pharmaceutical composition Substances 0.000 abstract description 4
239000000018 receptor agonist Substances 0.000 abstract description 4
229940044601 receptor agonist Drugs 0.000 abstract description 4
102100027499 5-hydroxytryptamine receptor 1B Human genes 0.000 abstract 1
101710138639 5-hydroxytryptamine receptor 1B Proteins 0.000 abstract 1
150000001875 compounds Chemical class 0.000 description 18
239000002552 dosage form Substances 0.000 description 11
230000009977 dual effect Effects 0.000 description 9
-1 iodohydrates Chemical class 0.000 description 9
239000012729 immediate-release (IR) formulation Substances 0.000 description 8
229960003708 sumatriptan Drugs 0.000 description 8
KQKPFRSPSRPDEB-UHFFFAOYSA-N sumatriptan Chemical compound CNS(=O)(=O)CC1=CC=C2NC=C(CCN(C)C)C2=C1 KQKPFRSPSRPDEB-UHFFFAOYSA-N 0.000 description 8
KRQUFUKTQHISJB-YYADALCUSA-N 2-[(E)-N-[2-(4-chlorophenoxy)propoxy]-C-propylcarbonimidoyl]-3-hydroxy-5-(thian-3-yl)cyclohex-2-en-1-one Chemical compound CCC\C(=N/OCC(C)OC1=CC=C(Cl)C=C1)C1=C(O)CC(CC1=O)C1CCCSC1 KRQUFUKTQHISJB-YYADALCUSA-N 0.000 description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
239000002775 capsule Substances 0.000 description 6
239000000243 solution Substances 0.000 description 6
ZISSAWUMDACLOM-UHFFFAOYSA-N triptane Chemical class CC(C)C(C)(C)C ZISSAWUMDACLOM-UHFFFAOYSA-N 0.000 description 6
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 5
239000002253 acid Substances 0.000 description 5
238000013270 controlled release Methods 0.000 description 4
239000012528 membrane Substances 0.000 description 4
239000012730 sustained-release form Substances 0.000 description 4
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
206010019233 Headaches Diseases 0.000 description 3
206010060860 Neurological symptom Diseases 0.000 description 3
239000000443 aerosol Substances 0.000 description 3
230000003628 erosive effect Effects 0.000 description 3
231100000869 headache Toxicity 0.000 description 3
239000008101 lactose Substances 0.000 description 3
239000011159 matrix material Substances 0.000 description 3
239000000546 pharmaceutical excipient Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
238000013268 sustained release Methods 0.000 description 3
208000024891 symptom Diseases 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
WKEMJKQOLOHJLZ-UHFFFAOYSA-N Almogran Chemical compound C1=C2C(CCN(C)C)=CNC2=CC=C1CS(=O)(=O)N1CCCC1 WKEMJKQOLOHJLZ-UHFFFAOYSA-N 0.000 description 2
GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
108010010803 Gelatin Proteins 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
208000000060 Migraine with aura Diseases 0.000 description 2
206010028813 Nausea Diseases 0.000 description 2
206010034960 Photophobia Diseases 0.000 description 2
229920002472 Starch Polymers 0.000 description 2
239000000556 agonist Substances 0.000 description 2
229960002133 almotriptan Drugs 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
239000011248 coating agent Substances 0.000 description 2
238000000576 coating method Methods 0.000 description 2
239000003086 colorant Substances 0.000 description 2
238000007906 compression Methods 0.000 description 2
230000006835 compression Effects 0.000 description 2
239000006071 cream Substances 0.000 description 2
230000001934 delay Effects 0.000 description 2
238000009792 diffusion process Methods 0.000 description 2
239000003085 diluting agent Substances 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000000945 filler Substances 0.000 description 2
239000000796 flavoring agent Substances 0.000 description 2
238000009472 formulation Methods 0.000 description 2
229960002284 frovatriptan Drugs 0.000 description 2
SIBNYOSJIXCDRI-SECBINFHSA-N frovatriptan Chemical compound C1=C(C(N)=O)[CH]C2=C(C[C@H](NC)CC3)C3=NC2=C1 SIBNYOSJIXCDRI-SECBINFHSA-N 0.000 description 2
210000001035 gastrointestinal tract Anatomy 0.000 description 2
239000008273 gelatin Substances 0.000 description 2
229920000159 gelatin Polymers 0.000 description 2
235000019322 gelatine Nutrition 0.000 description 2
235000011852 gelatine desserts Nutrition 0.000 description 2
239000006210 lotion Substances 0.000 description 2
239000000314 lubricant Substances 0.000 description 2
HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
206010052787 migraine without aura Diseases 0.000 description 2
239000002480 mineral oil Substances 0.000 description 2
235000010446 mineral oil Nutrition 0.000 description 2
229960005254 naratriptan Drugs 0.000 description 2
UNHGSHHVDNGCFN-UHFFFAOYSA-N naratriptan Chemical compound C=12[CH]C(CCS(=O)(=O)NC)=CC=C2N=CC=1C1CCN(C)CC1 UNHGSHHVDNGCFN-UHFFFAOYSA-N 0.000 description 2
230000008693 nausea Effects 0.000 description 2
239000006199 nebulizer Substances 0.000 description 2
231100000252 nontoxic Toxicity 0.000 description 2
230000003000 nontoxic effect Effects 0.000 description 2
239000002674 ointment Substances 0.000 description 2
235000019271 petrolatum Nutrition 0.000 description 2
229940068196 placebo Drugs 0.000 description 2
239000000902 placebo Substances 0.000 description 2
229920001223 polyethylene glycol Polymers 0.000 description 2
239000000843 powder Substances 0.000 description 2
102000005962 receptors Human genes 0.000 description 2
108020003175 receptors Proteins 0.000 description 2
230000000306 recurrent effect Effects 0.000 description 2
229960000425 rizatriptan Drugs 0.000 description 2
TXHZXHICDBAVJW-UHFFFAOYSA-N rizatriptan Chemical compound C=1[C]2C(CCN(C)C)=CN=C2C=CC=1CN1C=NC=N1 TXHZXHICDBAVJW-UHFFFAOYSA-N 0.000 description 2
239000000952 serotonin receptor agonist Substances 0.000 description 2
239000011734 sodium Substances 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000012453 solvate Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
239000008107 starch Substances 0.000 description 2
235000019698 starch Nutrition 0.000 description 2
238000007920 subcutaneous administration Methods 0.000 description 2
239000000725 suspension Substances 0.000 description 2
229960001360 zolmitriptan Drugs 0.000 description 2
UTAZCRNOSWWEFR-ZDUSSCGKSA-N zolmitriptan Chemical compound C=1[C]2C(CCN(C)C)=CN=C2C=CC=1C[C@H]1COC(=O)N1 UTAZCRNOSWWEFR-ZDUSSCGKSA-N 0.000 description 2
YFMFNYKEUDLDTL-UHFFFAOYSA-N 1,1,1,2,3,3,3-heptafluoropropane Chemical compound FC(F)(F)C(F)C(F)(F)F YFMFNYKEUDLDTL-UHFFFAOYSA-N 0.000 description 1
LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 description 1
DDMOUSALMHHKOS-UHFFFAOYSA-N 1,2-dichloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)(Cl)C(F)(F)Cl DDMOUSALMHHKOS-UHFFFAOYSA-N 0.000 description 1
FDCJDKXCCYFOCV-UHFFFAOYSA-N 1-hexadecoxyhexadecane Chemical compound CCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCC FDCJDKXCCYFOCV-UHFFFAOYSA-N 0.000 description 1
108091032151 5-hydroxytryptamine receptor family Proteins 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
OCUCCJIRFHNWBP-IYEMJOQQSA-L Copper gluconate Chemical class [Cu+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O OCUCCJIRFHNWBP-IYEMJOQQSA-L 0.000 description 1
239000004338 Dichlorodifluoromethane Substances 0.000 description 1
102000014630 G protein-coupled serotonin receptor activity proteins Human genes 0.000 description 1
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
239000004471 Glycine Substances 0.000 description 1
229920000084 Gum arabic Polymers 0.000 description 1
208000027109 Headache disease Diseases 0.000 description 1
239000004705 High-molecular-weight polyethylene Substances 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
229920000168 Microcrystalline cellulose Polymers 0.000 description 1
206010027603 Migraine headaches Diseases 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
239000004264 Petrolatum Substances 0.000 description 1
206010034912 Phobia Diseases 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
229920001214 Polysorbate 60 Polymers 0.000 description 1
241001282135 Poromitra oscitans Species 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
208000037048 Prodromal Symptoms Diseases 0.000 description 1
229920001800 Shellac Polymers 0.000 description 1
229920002125 Sokalan® Chemical class 0.000 description 1
HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
239000004147 Sorbitan trioleate Substances 0.000 description 1
PRXRUNOAOLTIEF-ADSICKODSA-N Sorbitan trioleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCC\C=C/CCCCCCCC PRXRUNOAOLTIEF-ADSICKODSA-N 0.000 description 1
229930006000 Sucrose Natural products 0.000 description 1
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
206010048232 Yawning Diseases 0.000 description 1
239000000205 acacia gum Substances 0.000 description 1
235000010489 acacia gum Nutrition 0.000 description 1
150000001242 acetic acid derivatives Chemical class 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000003957 anion exchange resin Substances 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical class OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
150000001558 benzoic acid derivatives Chemical class 0.000 description 1
235000019445 benzyl alcohol Nutrition 0.000 description 1
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-M bisulphate group Chemical group S([O-])(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 description 1
239000008280 blood Substances 0.000 description 1
210000004369 blood Anatomy 0.000 description 1
230000037396 body weight Effects 0.000 description 1
210000004556 brain Anatomy 0.000 description 1
210000000133 brain stem Anatomy 0.000 description 1
150000001649 bromium compounds Chemical class 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
239000001506 calcium phosphate Substances 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
210000003710 cerebral cortex Anatomy 0.000 description 1
229940081733 cetearyl alcohol Drugs 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
150000001805 chlorine compounds Chemical class 0.000 description 1
150000001860 citric acid derivatives Chemical class 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
239000007771 core particle Substances 0.000 description 1
235000019788 craving Nutrition 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
239000007933 dermal patch Substances 0.000 description 1
PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
229940087091 dichlorotetrafluoroethane Drugs 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
239000007884 disintegrant Substances 0.000 description 1
208000035475 disorder Diseases 0.000 description 1
239000008298 dragée Substances 0.000 description 1
239000003937 drug carrier Substances 0.000 description 1
239000000975 dye Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
239000008387 emulsifying waxe Substances 0.000 description 1
CCIVGXIOQKPBKL-UHFFFAOYSA-N ethanesulfonic acid Chemical class CCS(O)(=O)=O CCIVGXIOQKPBKL-UHFFFAOYSA-N 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000012530 fluid Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
235000013355 food flavoring agent Nutrition 0.000 description 1
235000003599 food sweetener Nutrition 0.000 description 1
VZCYOOQTPOCHFL-OWOJBTEDSA-L fumarate(2-) Chemical class [O-]C(=O)\C=C\C([O-])=O VZCYOOQTPOCHFL-OWOJBTEDSA-L 0.000 description 1
239000008103 glucose Substances 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 description 1
238000005469 granulation Methods 0.000 description 1
230000003179 granulation Effects 0.000 description 1
150000004677 hydrates Chemical class 0.000 description 1
150000005828 hydrofluoroalkanes Chemical class 0.000 description 1
238000001802 infusion Methods 0.000 description 1
238000005342 ion exchange Methods 0.000 description 1
150000003893 lactate salts Chemical class 0.000 description 1
239000007788 liquid Substances 0.000 description 1
229940057995 liquid paraffin Drugs 0.000 description 1
230000004807 localization Effects 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
235000019359 magnesium stearate Nutrition 0.000 description 1
150000002688 maleic acid derivatives Chemical class 0.000 description 1
210000002418 meninge Anatomy 0.000 description 1
AFVFQIVMOAPDHO-UHFFFAOYSA-M methanesulfonate group Chemical class CS(=O)(=O)[O-] AFVFQIVMOAPDHO-UHFFFAOYSA-M 0.000 description 1
239000008108 microcrystalline cellulose Substances 0.000 description 1
229940016286 microcrystalline cellulose Drugs 0.000 description 1
235000019813 microcrystalline cellulose Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
150000002823 nitrates Chemical class 0.000 description 1
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 1
230000003204 osmotic effect Effects 0.000 description 1
238000007911 parenteral administration Methods 0.000 description 1
229940066842 petrolatum Drugs 0.000 description 1
239000008024 pharmaceutical diluent Substances 0.000 description 1
229940124531 pharmaceutical excipient Drugs 0.000 description 1
230000000144 pharmacologic effect Effects 0.000 description 1
208000019899 phobic disease Diseases 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
230000037081 physical activity Effects 0.000 description 1
239000006187 pill Substances 0.000 description 1
229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
239000004584 polyacrylic acid Chemical class 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000001818 polyoxyethylene sorbitan monostearate Substances 0.000 description 1
235000010989 polyoxyethylene sorbitan monostearate Nutrition 0.000 description 1
229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
229940113124 polysorbate 60 Drugs 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
239000011148 porous material Substances 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000003380 propellant Substances 0.000 description 1
235000013772 propylene glycol Nutrition 0.000 description 1
230000002285 radioactive effect Effects 0.000 description 1
229940113147 shellac Drugs 0.000 description 1
239000004208 shellac Substances 0.000 description 1
ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
235000013874 shellac Nutrition 0.000 description 1
210000001599 sigmoid colon Anatomy 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000001509 sodium citrate Substances 0.000 description 1
NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
229940006186 sodium polystyrene sulfonate Drugs 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
239000001587 sorbitan monostearate Substances 0.000 description 1
235000011076 sorbitan monostearate Nutrition 0.000 description 1
229940035048 sorbitan monostearate Drugs 0.000 description 1
235000019337 sorbitan trioleate Nutrition 0.000 description 1
229960000391 sorbitan trioleate Drugs 0.000 description 1
239000007921 spray Substances 0.000 description 1
150000003890 succinate salts Chemical class 0.000 description 1
239000005720 sucrose Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000000829 suppository Substances 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
230000002459 sustained effect Effects 0.000 description 1
239000003765 sweetening agent Substances 0.000 description 1
239000003826 tablet Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
150000003892 tartrate salts Chemical class 0.000 description 1
230000000699 topical effect Effects 0.000 description 1
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
229940078499 tricalcium phosphate Drugs 0.000 description 1
229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
235000019731 tricalcium phosphate Nutrition 0.000 description 1
CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
229940029284 trichlorofluoromethane Drugs 0.000 description 1
230000001960 triggered effect Effects 0.000 description 1
229940120293 vaginal suppository Drugs 0.000 description 1
239000006216 vaginal suppository Substances 0.000 description 1
239000001993 wax Substances 0.000 description 1
239000003871 white petrolatum Substances 0.000 description 1
150000003751 zinc Chemical class 0.000 description 1

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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
- 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
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
- A61K31/4045—Indole-alkylamines; Amides thereof, e.g. serotonin, melatonin
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4196—1,2,4-Triazoles
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
- A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
- 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
- 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
- A61P25/08—Antiepileptics; Anticonvulsants

Landscapes

Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
General Health & Medical Sciences (AREA)
Animal Behavior & Ethology (AREA)
Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Pharmacology & Pharmacy (AREA)
Epidemiology (AREA)
Neurosurgery (AREA)
Bioinformatics & Cheminformatics (AREA)
Organic Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Neurology (AREA)
Biomedical Technology (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Engineering & Computer Science (AREA)
Pain & Pain Management (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Medicinal Preparation (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Medicines Containing Plant Substances (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

UA2001010653A 1998-07-30 1999-06-14 Use of eletriptan for prevention of migraine recurrence UA76399C2 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GBGB9816556.6A GB9816556D0 (en)	1998-07-30	1998-07-30	Therapy
PCT/IB1999/001105 WO2000006161A1 (en)	1998-07-30	1999-06-14	Prevention of migraine recurrence

Publications (1)

Publication Number	Publication Date
UA76399C2 true UA76399C2 (en)	2006-08-15

Family

ID=10836395

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
UA2001010653A UA76399C2 (en)	1998-07-30	1999-06-14	Use of eletriptan for prevention of migraine recurrence

Country Status (35)

Country	Link
EP (3)	EP1100499B1 (id)
JP (1)	JP3824863B2 (id)
KR (2)	KR100441732B1 (id)
CN (2)	CN1522697A (id)
AP (1)	AP1402A (id)
AT (1)	ATE261304T1 (id)
AU (1)	AU3952199A (id)
BG (1)	BG65309B1 (id)
BR (1)	BR9912588A (id)
CA (1)	CA2338901C (id)
CZ (1)	CZ2001357A3 (id)
DE (1)	DE69915486T2 (id)
DK (1)	DK1100499T3 (id)
EA (2)	EA200201149A1 (id)
EE (1)	EE04703B1 (id)
ES (1)	ES2214027T3 (id)
GB (1)	GB9816556D0 (id)
GE (2)	GEP20063719B (id)
HR (1)	HRP20010079A2 (id)
HU (1)	HUP0103424A3 (id)
ID (1)	ID26996A (id)
IL (1)	IL140169A0 (id)
IS (1)	IS2253B (id)
NO (1)	NO20010489L (id)
NZ (2)	NZ508736A (id)
OA (1)	OA11576A (id)
PL (1)	PL194611B1 (id)
PT (1)	PT1100499E (id)
SG (1)	SG125910A1 (id)
SK (1)	SK1182001A3 (id)
TR (1)	TR200100314T2 (id)
TW (2)	TWI248362B (id)
UA (1)	UA76399C2 (id)
WO (1)	WO2000006161A1 (id)
YU (2)	YU20303A (id)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US8022095B2 (en)	1996-08-16	2011-09-20	Pozen, Inc.	Methods of treating headaches using 5-HT agonists in combination with long-acting NSAIDs
GB9915231D0 (en) *	1999-06-29	1999-09-01	Pfizer Ltd	Pharmaceutical complex
CN1176649C (zh) *	2002-10-16	2004-11-24	上海医药工业研究院	舒马普坦干粉吸入剂及其制备方法
WO2004060355A1 (en) *	2002-12-26	2004-07-22	Pozen Inc.	Multilayer Dosage Forms Containing NSAIDs and Triptans
JP2006522790A (ja)	2003-04-11	2006-10-05	ファイザー・インク	エレトリプタンと重炭酸ナトリウムを含む医薬組み合わせ物
GB2407498B (en) *	2003-10-30	2008-06-11	Cipla Ltd	Oral formulations for 5-HT receptor agonists with reduced degradation of active ingredient
FR2926721B1 (fr) *	2008-01-30	2011-07-22	Philippe Perovitch	Forme galenique pour l'adminsitration par voie trans-muqueuse de triptans
CA2765866C (en)	2008-06-20	2016-06-21	Alphapharm Pty Ltd	Single phase pharmaceutical composition of a 5-ht1 inhibitor and an nsaid
EP2490669B1 (en) *	2009-10-23	2017-01-11	Fortuderm Ltd.	Triptans for the treatment of psoriasis
NZ700474A (en) *	2012-04-18	2016-10-28	Contera Pharma Aps	Orally available pharmaceutical formulation suitable for improved management of movement disorders
CN103385876B (zh) *	2012-05-08	2016-01-13	四川滇虹医药开发有限公司	一种夫罗曲坦的药物组合物及其制备方法
CN104523709A (zh) *	2014-12-22	2015-04-22	青岛正大海尔制药有限公司	一种含有琥珀酸夫罗曲坦的复方缓释制剂
AU2017297718B2 (en)	2016-07-11	2023-06-08	Contera Pharma A/S	Pulsatile drug delivery system for treating morning akinesia

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
PL170330B1 (pl) *	1990-10-15	1996-11-29	Pfizer	Sposób wytwarzania nowych pochodnych indolu PL PL PL PL PL PL
DE69222006T2 (de) *	1991-10-30	1998-01-22	Glaxo Group Ltd	Mehrschichtzusammensetzungen enthaltend Histamin- oder Serotonin- Antagonisten
US5464633A (en) *	1994-05-24	1995-11-07	Jagotec Ag	Pharmaceutical tablets releasing the active substance after a definite period of time
GB9417310D0 (en) *	1994-08-27	1994-10-19	Pfizer Ltd	Therapeutic agents
US5698571A (en) *	1994-10-05	1997-12-16	Eli Lilly And Company	5-HT1F mediated inhibition of neurogenic meningeal extravasation: a method for the treatment of migraine
US5744482A (en) *	1994-10-05	1998-04-28	Eli Lilly And Company	Serotonin agonist in combination with a tachykinin receptor antagonist in the treatment or prevention of migraine
US6255502B1 (en) *	1996-07-11	2001-07-03	Farmarc Nederland B.V.	Pharmaceutical composition containing acid addition salt of basic drug
PL337803A1 (en) *	1997-07-03	2000-09-11	Pfizer	Pharmaceutic agents containing eletriptane hemisulphate and caffeine
US6514530B2 (en) *	1997-09-09	2003-02-04	Alza Corporation	Dosage form comprising means for changing drug delivery shape

1998
- 1998-07-30 GB GBGB9816556.6A patent/GB9816556D0/en not_active Ceased
1999
- 1999-06-14 PL PL99345803A patent/PL194611B1/pl not_active IP Right Cessation
- 1999-06-14 SK SK118-2001A patent/SK1182001A3/sk unknown
- 1999-06-14 JP JP2000562016A patent/JP3824863B2/ja not_active Expired - Fee Related
- 1999-06-14 CN CNA2003101025101A patent/CN1522697A/zh active Pending
- 1999-06-14 KR KR10-2001-7001231A patent/KR100441732B1/ko not_active Expired - Fee Related
- 1999-06-14 CZ CZ2001357A patent/CZ2001357A3/cs unknown
- 1999-06-14 HR HR20010079A patent/HRP20010079A2/hr not_active Application Discontinuation
- 1999-06-14 YU YU20303A patent/YU20303A/sh unknown
- 1999-06-14 IL IL14016999A patent/IL140169A0/xx unknown
- 1999-06-14 KR KR10-2003-7008744A patent/KR20030078876A/ko not_active Ceased
- 1999-06-14 CA CA002338901A patent/CA2338901C/en not_active Expired - Fee Related
- 1999-06-14 EA EA200201149A patent/EA200201149A1/ru unknown
- 1999-06-14 ES ES99922459T patent/ES2214027T3/es not_active Expired - Lifetime
- 1999-06-14 DE DE69915486T patent/DE69915486T2/de not_active Expired - Fee Related
- 1999-06-14 UA UA2001010653A patent/UA76399C2/uk unknown
- 1999-06-14 PT PT99922459T patent/PT1100499E/pt unknown
- 1999-06-14 SG SG200300769A patent/SG125910A1/en unknown
- 1999-06-14 ID IDW20010229A patent/ID26996A/id unknown
- 1999-06-14 NZ NZ508736A patent/NZ508736A/en unknown
- 1999-06-14 CN CNB998087378A patent/CN1155379C/zh not_active Expired - Fee Related
- 1999-06-14 DK DK99922459T patent/DK1100499T3/da active
- 1999-06-14 BR BR9912588-9A patent/BR9912588A/pt not_active Application Discontinuation
- 1999-06-14 AU AU39521/99A patent/AU3952199A/en not_active Abandoned
- 1999-06-14 EP EP99922459A patent/EP1100499B1/en not_active Expired - Lifetime
- 1999-06-14 HU HU0103424A patent/HUP0103424A3/hu unknown
- 1999-06-14 GE GEAP19996881A patent/GEP20063719B/en unknown
- 1999-06-14 YU YU6401A patent/YU6401A/sh unknown
- 1999-06-14 AP APAP/P/2001/002056A patent/AP1402A/en active
- 1999-06-14 EA EA200100089A patent/EA004036B1/ru not_active IP Right Cessation
- 1999-06-14 AT AT99922459T patent/ATE261304T1/de not_active IP Right Cessation
- 1999-06-14 EP EP04004644A patent/EP1435237A1/en not_active Withdrawn
- 1999-06-14 GE GEAP19995732A patent/GEP20043157B/en unknown
- 1999-06-14 WO PCT/IB1999/001105 patent/WO2000006161A1/en not_active Ceased
- 1999-06-14 TR TR2001/00314T patent/TR200100314T2/xx unknown
- 1999-06-14 OA OA1200000354A patent/OA11576A/en unknown
- 1999-06-14 EP EP04004643A patent/EP1466601A3/en not_active Withdrawn
- 1999-06-14 EE EEP200100061A patent/EE04703B1/xx not_active IP Right Cessation
- 1999-06-17 TW TW092102563A patent/TWI248362B/zh not_active IP Right Cessation
- 1999-06-17 TW TW088110233A patent/TW537893B/zh not_active IP Right Cessation
2000
- 2000-12-15 IS IS5771A patent/IS2253B/is unknown
2001
- 2001-01-29 NO NO20010489A patent/NO20010489L/no not_active Application Discontinuation
- 2001-02-20 BG BG105277A patent/BG65309B1/bg unknown
2003
- 2003-08-15 NZ NZ527625A patent/NZ527625A/en unknown

Also Published As

Publication number	Publication date
GEP20063719B (en)	2006-01-10
IL140169A0 (en)	2002-02-10
EP1466601A3 (en)	2005-04-13
EE200100061A (et)	2002-06-17
HRP20010079A2 (en)	2002-02-28
ES2214027T3 (es)	2004-09-01
CN1522697A (zh)	2004-08-25
CA2338901C (en)	2008-02-19
JP3824863B2 (ja)	2006-09-20
CZ2001357A3 (cs)	2001-10-17
DE69915486D1 (de)	2004-04-15
EE04703B1 (et)	2006-10-16
EP1466601A2 (en)	2004-10-13
TR200100314T2 (tr)	2001-06-21
TW200300674A (en)	2003-06-16
EP1100499A1 (en)	2001-05-23
YU6401A (sh)	2004-03-12
SK1182001A3 (en)	2001-10-08
OA11576A (en)	2004-07-01
BG105277A (en)	2001-11-30
PL345803A1 (en)	2002-01-02
AU3952199A (en)	2000-02-21
DE69915486T2 (de)	2005-03-03
KR20010079582A (ko)	2001-08-22
BG65309B1 (bg)	2008-01-31
EP1435237A1 (en)	2004-07-07
PT1100499E (pt)	2004-06-30
EA200100089A1 (ru)	2001-08-27
NO20010489L (no)	2001-03-26
GB9816556D0 (en)	1998-09-30
GEP20043157B (en)	2004-01-26
EA004036B1 (ru)	2003-12-25
AP1402A (en)	2005-04-29
CA2338901A1 (en)	2000-02-10
KR100441732B1 (ko)	2004-07-27
NZ508736A (en)	2003-09-26
YU20303A (sh)	2006-08-17
CN1155379C (zh)	2004-06-30
BR9912588A (pt)	2001-05-02
IS2253B (is)	2007-06-15
HK1038198A1 (en)	2002-03-08
HUP0103424A2 (hu)	2002-02-28
PL194611B1 (pl)	2007-06-29
AP2001002056A0 (en)	2001-03-31
ATE261304T1 (de)	2004-03-15
EA200201149A1 (ru)	2003-02-27
HUP0103424A3 (en)	2003-05-28
KR20030078876A (ko)	2003-10-08
EP1100499B1 (en)	2004-03-10
IS5771A (is)	2000-12-15
JP2002521446A (ja)	2002-07-16
TWI248362B (en)	2006-02-01
SG125910A1 (en)	2006-10-30
WO2000006161A1 (en)	2000-02-10
CN1309560A (zh)	2001-08-22
TW537893B (en)	2003-06-21
NZ527625A (en)	2005-01-28
DK1100499T3 (da)	2004-06-14
NO20010489D0 (no)	2001-01-29
ID26996A (id)	2001-02-22

Publication	Publication Date	Title
JP2003522145A (ja)	2003-07-22	セントラルカンナビノイドレセプター拮抗剤のタバコ消費を止める助けに有用である医薬品への使用
UA76399C2 (en)	2006-08-15	Use of eletriptan for prevention of migraine recurrence
MXPA06004846A (es)	2006-07-06	Formulaciones orales para agonistas del receptor de 5-ht, usos y metodos de tratamiento que emplean las mismas.
US20020099059A1 (en)	2002-07-25	Combination therapy for the treatment of migraine
WO2023177294A1 (en)	2023-09-21	Transmucosal delivery of psychoactive compounds
JP2009535336A (ja)	2009-10-01	片頭痛治療用の固定組合せ剤形
US20080161307A1 (en)	2008-07-03	Organic Compounds
AU2004222771B2 (en)	2006-09-21	Prevention of Migraine Recurrence
JP2006522790A (ja)	2006-10-05	エレトリプタンと重炭酸ナトリウムを含む医薬組み合わせ物
MXPA01001097A (en)	2001-11-21	Prevention of migraine recurrence
AU2003213493A1 (en)	2003-08-14	Prevention of Migraine Recurrence
US20030018031A1 (en)	2003-01-23	Formulations of 5HT agonists
HK1064618A (en)	2005-02-04	A composition for preventing migraine recurrence
JP2003516349A (ja)	2003-05-13	スマトリプタンまたはナラトリプタンとシクロオキシゲナーゼインヒビターの組み合わせ