CA2278201C - Novel modifications to 2-amino-4-(4-fluorobenzylamino)-1-ethoxycarbonyl-aminobenzene, and processes for their preparation - Google Patents
Novel modifications to 2-amino-4-(4-fluorobenzylamino)-1-ethoxycarbonyl-aminobenzene, and processes for their preparation Download PDFInfo
- Publication number
- CA2278201C CA2278201C CA002278201A CA2278201A CA2278201C CA 2278201 C CA2278201 C CA 2278201C CA 002278201 A CA002278201 A CA 002278201A CA 2278201 A CA2278201 A CA 2278201A CA 2278201 C CA2278201 C CA 2278201C
- Authority
- CA
- Canada
- Prior art keywords
- ang
- preparation
- compound
- crystalline form
- modification
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title claims abstract description 14
- 238000002360 preparation method Methods 0.000 title claims description 15
- 230000004048 modification Effects 0.000 title abstract description 62
- 238000012986 modification Methods 0.000 title abstract description 62
- IIWRHAXIPLGNJO-UHFFFAOYSA-N ethyl 2,3-diamino-4-[(4-fluorophenyl)methylamino]benzoate Chemical compound NC1=C(N)C(C(=O)OCC)=CC=C1NCC1=CC=C(F)C=C1 IIWRHAXIPLGNJO-UHFFFAOYSA-N 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 33
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Natural products CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 26
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 20
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 15
- 239000013078 crystal Substances 0.000 claims description 14
- 238000002425 crystallisation Methods 0.000 claims description 13
- 230000008025 crystallization Effects 0.000 claims description 13
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 8
- 239000000010 aprotic solvent Substances 0.000 claims description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical group CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 6
- 239000000825 pharmaceutical preparation Substances 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 239000012454 non-polar solvent Substances 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- 239000003586 protic polar solvent Substances 0.000 claims description 4
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000003944 tolyl group Chemical group 0.000 claims 1
- 239000000243 solution Substances 0.000 description 10
- 230000000694 effects Effects 0.000 description 7
- 238000001938 differential scanning calorimetry curve Methods 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000002329 infrared spectrum Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000010792 warming Methods 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000012047 saturated solution Substances 0.000 description 2
- 238000010583 slow cooling Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910016523 CuKa Inorganic materials 0.000 description 1
- 230000000202 analgesic effect Effects 0.000 description 1
- 230000002082 anti-convulsion Effects 0.000 description 1
- 230000001754 anti-pyretic effect Effects 0.000 description 1
- 239000001961 anticonvulsive agent Substances 0.000 description 1
- 239000002221 antipyretic Substances 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- PCOBBVZJEWWZFR-UHFFFAOYSA-N ezogabine Chemical compound C1=C(N)C(NC(=O)OCC)=CC=C1NCC1=CC=C(F)C=C1 PCOBBVZJEWWZFR-UHFFFAOYSA-N 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- -1 for example Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004090 neuroprotective agent Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/26—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring
- C07C271/28—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring to a carbon atom of a non-condensed six-membered aromatic ring
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pain & Pain Management (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Biomedical Technology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Rheumatology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA2634811A CA2634811C (en) | 1997-01-20 | 1998-01-09 | Novel modifications to 2-amino-4-(4-fluorobenzylamino) -1- ethoxycarbonyl-aminobenzene and processes for preparing said compound |
| CA2632585A CA2632585C (en) | 1997-01-20 | 1998-01-09 | Novel modifications to 2-amino-4-(4-fluorobenzylamino)-1-ethoxycarbonyl-aminobenzene and processes for preparing said compound |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19701694.4 | 1997-01-20 | ||
| DE19701694A DE19701694A1 (de) | 1997-01-20 | 1997-01-20 | Neue Modifikationen des 2-Amino-4-(4-fluorbenzylamino)-l-ethoxycarbonyl-aminobenzen sowie Verfahren zu ihrer Herstellung |
| PCT/EP1998/000086 WO1998031663A1 (de) | 1997-01-20 | 1998-01-09 | Neue modifikationen des 2-amino-4-(4-fluorbenzylamino)-1-ethoxycarbonyl-aminobenzen sowie verfahren zu ihrer herstellung |
Related Child Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2632585A Division CA2632585C (en) | 1997-01-20 | 1998-01-09 | Novel modifications to 2-amino-4-(4-fluorobenzylamino)-1-ethoxycarbonyl-aminobenzene and processes for preparing said compound |
| CA2634811A Division CA2634811C (en) | 1997-01-20 | 1998-01-09 | Novel modifications to 2-amino-4-(4-fluorobenzylamino) -1- ethoxycarbonyl-aminobenzene and processes for preparing said compound |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2278201A1 CA2278201A1 (en) | 1998-07-23 |
| CA2278201C true CA2278201C (en) | 2009-06-16 |
Family
ID=7817756
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002278201A Expired - Lifetime CA2278201C (en) | 1997-01-20 | 1998-01-09 | Novel modifications to 2-amino-4-(4-fluorobenzylamino)-1-ethoxycarbonyl-aminobenzene, and processes for their preparation |
| CA2632585A Expired - Lifetime CA2632585C (en) | 1997-01-20 | 1998-01-09 | Novel modifications to 2-amino-4-(4-fluorobenzylamino)-1-ethoxycarbonyl-aminobenzene and processes for preparing said compound |
| CA2634811A Expired - Lifetime CA2634811C (en) | 1997-01-20 | 1998-01-09 | Novel modifications to 2-amino-4-(4-fluorobenzylamino) -1- ethoxycarbonyl-aminobenzene and processes for preparing said compound |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2632585A Expired - Lifetime CA2632585C (en) | 1997-01-20 | 1998-01-09 | Novel modifications to 2-amino-4-(4-fluorobenzylamino)-1-ethoxycarbonyl-aminobenzene and processes for preparing said compound |
| CA2634811A Expired - Lifetime CA2634811C (en) | 1997-01-20 | 1998-01-09 | Novel modifications to 2-amino-4-(4-fluorobenzylamino) -1- ethoxycarbonyl-aminobenzene and processes for preparing said compound |
Country Status (30)
| Country | Link |
|---|---|
| US (2) | US5914425A (enExample) |
| EP (1) | EP0956281B1 (enExample) |
| JP (1) | JP4138886B2 (enExample) |
| CN (1) | CN1125812C (enExample) |
| AR (1) | AR015349A1 (enExample) |
| AT (1) | ATE222235T1 (enExample) |
| AU (1) | AU730776B2 (enExample) |
| BG (1) | BG63893B1 (enExample) |
| BR (1) | BR9806784A (enExample) |
| CA (3) | CA2278201C (enExample) |
| CZ (1) | CZ301778B6 (enExample) |
| DE (2) | DE19701694A1 (enExample) |
| DK (1) | DK0956281T3 (enExample) |
| EG (1) | EG21239A (enExample) |
| ES (1) | ES2178152T3 (enExample) |
| HU (1) | HU227625B1 (enExample) |
| ID (1) | ID22645A (enExample) |
| IL (1) | IL130384A (enExample) |
| IS (1) | IS2115B (enExample) |
| NO (2) | NO311642B1 (enExample) |
| NZ (1) | NZ336205A (enExample) |
| PL (1) | PL195956B1 (enExample) |
| PT (1) | PT956281E (enExample) |
| RU (1) | RU2186765C2 (enExample) |
| SK (1) | SK285303B6 (enExample) |
| TR (1) | TR199901674T2 (enExample) |
| TW (1) | TW531527B (enExample) |
| UA (1) | UA63937C2 (enExample) |
| WO (1) | WO1998031663A1 (enExample) |
| ZA (1) | ZA98319B (enExample) |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6348486B1 (en) | 2000-10-17 | 2002-02-19 | American Home Products Corporation | Methods for modulating bladder function |
| US6589986B2 (en) | 2000-12-20 | 2003-07-08 | Wyeth | Methods of treating anxiety disorders |
| AU2002338333A1 (en) * | 2001-04-04 | 2002-10-21 | Wyeth | Methods for treating hyperactive gastric motility |
| US7799832B2 (en) * | 2003-10-23 | 2010-09-21 | Valeant Pharmaceuticals North America | Combinations of retigabine and sodium channel inhibitors or sodium channel-influencing active compounds for treating pains |
| US7960436B2 (en) * | 2006-06-05 | 2011-06-14 | Valeant Pharmaceuticals International | Substituted arylamino-1,2,3,4-tetrahydro naphthalenes and-2,3-dihydro-1H-indenes as potassium channel modulators |
| US20080045534A1 (en) * | 2006-08-18 | 2008-02-21 | Valeant Pharmaceuticals North America | Derivatives of 1,3-diamino benzene as potassium channel modulators |
| US8993593B2 (en) * | 2006-08-23 | 2015-03-31 | Valeant Pharmaceuticals International | N-(4-(6-fluoro-3,4-dihydroisoquinolin-2(1H)-yl)-2,6-dimethylphenyl)-3,3-dimethylbutanamide as potassium channel modulators |
| KR20090079191A (ko) * | 2006-08-23 | 2009-07-21 | 밞늬ìžíž íë§ìí°ì»¬ìŠ ìží°ëŽì ë | 칌륚 ì±ë ì¡°ì ì ë¡ì ïŒ-(ïœ-ììì¬ìŽíŽë¡ìí¬) ìë늬ëì ì ë첎 |
| US8722929B2 (en) * | 2006-10-10 | 2014-05-13 | Valeant Pharmaceuticals International | N-[2-amino-4-(phenylmethoxy)phenyl] amides and related compounds as potassium channel modulators |
| US8030518B2 (en) * | 2006-11-28 | 2011-10-04 | Valeant Pharmaceuticals International | 1,4 diamino bicyclic retigabine analogues as potassium channel modulators |
| US8367684B2 (en) * | 2007-06-13 | 2013-02-05 | Valeant Pharmaceuticals International | Derivatives of 4-(N-azacycloalkyl) anilides as potassium channel modulators |
| US8563566B2 (en) | 2007-08-01 | 2013-10-22 | Valeant Pharmaceuticals International | Naphthyridine derivatives as potassium channel modulators |
| US7786146B2 (en) * | 2007-08-13 | 2010-08-31 | Valeant Pharmaceuticals International | Derivatives of 5-amino-4,6-disubstituted indole and 5-amino-4,6-disubstituted indoline as potassium channel modulators |
| US20100323016A1 (en) * | 2008-07-18 | 2010-12-23 | Biljana Nadjsombati | Modified release formulation and methods of use |
| US20100323015A1 (en) * | 2008-07-18 | 2010-12-23 | Biljana Nadjsombati | Modified release formulation and methods of use |
| NZ590885A (en) * | 2008-07-18 | 2013-01-25 | Valeant Pharmaceuticals Int | A modified release pharmaceutical formulation of retigabine for the treatment of nervous system hyperexcitability |
| DE102009013613A1 (de) | 2009-03-17 | 2010-09-23 | Ratiopharm Gmbh | Trockenverarbeitung von Retigabin |
| DE102009013611A1 (de) | 2009-03-17 | 2010-09-23 | Ratiopharm Gmbh | Festes Retigabin in nicht-kristalliner Form |
| DE102009013612A1 (de) | 2009-03-17 | 2010-09-23 | Ratiopharm Gmbh | Retigabin-Tabletten, bevorzugt mit modifizierter Freisetzung |
| WO2011039369A2 (en) | 2009-10-02 | 2011-04-07 | Medichem S.A. | Amorphous forms of a 2-amino-4-(4-fluorobenzylamino)phenylcarbamate derivative |
| EP2525788A2 (en) | 2010-01-20 | 2012-11-28 | Glaxo Group Limited | Novel retigabine composition |
| US20130131164A1 (en) * | 2010-02-19 | 2013-05-23 | Medichem, S.A. | Stabilized phenylcarbamate derivative in solid state |
| CN202095728U (zh) | 2010-10-29 | 2012-01-04 | åæ¥éå¢æ§è¡æéå ¬åž | è¡æç®±ææ |
| CN102464233A (zh) * | 2010-11-18 | 2012-05-23 | æ±èéŠåšæºæ¢°å¶é æéå ¬åž | äžç§å§åŒå·®éçŒ äžæºçšåºååçè£ çœ® |
| SG191309A1 (en) | 2011-01-18 | 2013-07-31 | Glaxo Group Ltd | Process for the preparation of retigabine |
| CN102241608A (zh) * | 2011-05-12 | 2011-11-16 | 倩接åžæ±åº·å»è¯çç©ææ¯æéå ¬åž | çæ¿å 滚ååç©åå ¶ç»åç© |
| WO2013008250A2 (en) * | 2011-07-01 | 2013-01-17 | Dr.Reddys Laboratories Limited. | Crystalline form of retigabine and processes for mixture of retigabine crystalline modifications |
| WO2013011518A1 (en) | 2011-07-21 | 2013-01-24 | Arch Pharmalabs Limited | Process for the preparation of retigabine of the formula i and pharmaceutically acceptable salts thereof |
| USD696019S1 (en) | 2011-10-21 | 2013-12-24 | Travelpro International Inc. | Handle for luggage |
| CN102531966B (zh) * | 2011-12-23 | 2013-07-24 | å±±äžåæ°è¯ç©ç åæéå ¬åž | çæ¿å 滚çæ¶ådåå ¶å¶å€æ¹æ³ |
| WO2013114379A1 (en) * | 2012-01-30 | 2013-08-08 | Symed Labs Limited | Novel polymorphs of n-[2-amino-4-(4-fluorobenzylamino)-phenyl] carbamic acid ethyl ester and processes thereof |
| CN103373941B (zh) * | 2012-04-11 | 2016-08-17 | æµæ±ä¹æŽ²è¯ç©ç§ææéå ¬åž | çæ¿å 滚åå ¶äžéŽäœçå¶å€æ¹æ³ |
| WO2013179298A2 (en) * | 2012-04-23 | 2013-12-05 | Cadila Healthcare Limited | A process for preparation of phenyl carbamate derivative and polymorphic forms thereof |
| WO2014023270A1 (en) | 2012-08-09 | 2014-02-13 | Zentiva, K.S. | Salts or co-crystals of ethyl n-[2-amino-4-[(4-fluorophenyl)methylamino]-phenyl]carbamate |
| CN102964273B (zh) * | 2012-12-06 | 2014-04-02 | å京è±ç§åé ç§ææéå ¬åž | çæ¿å 滚çæ°æ¶åfåå ¶å¶å€æ¹æ³ |
| USD773819S1 (en) | 2015-05-27 | 2016-12-13 | Travelpro Products, Inc. | Handle for luggage |
| TWI886158B (zh) | 2019-10-10 | 2025-06-11 | å æ¿å€§åå諟補è¥å ¬åž | éžææ§ééé調ç¯åä¹åºæ æ¶å |
| TW202128162A (zh) | 2019-11-08 | 2021-08-01 | å æ¿å€§åå諟補è¥å ¬åž | æ鬱çä¹æ²»çæ¹æ³ |
| AU2022220675A1 (en) | 2021-02-09 | 2023-09-21 | Xenon Pharmaceuticals Inc. | Voltage-gated potassium channel opener for use in treating anhedonia |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3917113A1 (de) * | 1989-05-26 | 1990-11-29 | Schwarzkopf Gmbh Hans | Verfahren zur selektiven herstellung von n(pfeil hoch)4(pfeil hoch)-substituierten 1,4-diamino-2-nitrobenzolen |
| GB8921792D0 (en) * | 1989-09-27 | 1989-11-08 | May & Baker Ltd | New compositions of matter |
| DE4200259A1 (de) * | 1992-01-08 | 1993-07-15 | Asta Medica Ag | Neue 1,2,4-triaminobenzol-derivate und verfahren zu deren herstellung |
-
1997
- 1997-01-20 DE DE19701694A patent/DE19701694A1/de not_active Ceased
-
1998
- 1998-01-09 PT PT98904048T patent/PT956281E/pt unknown
- 1998-01-09 BR BR9806784-2A patent/BR9806784A/pt not_active Application Discontinuation
- 1998-01-09 CA CA002278201A patent/CA2278201C/en not_active Expired - Lifetime
- 1998-01-09 SK SK956-99A patent/SK285303B6/sk not_active IP Right Cessation
- 1998-01-09 WO PCT/EP1998/000086 patent/WO1998031663A1/de not_active Ceased
- 1998-01-09 NZ NZ336205A patent/NZ336205A/xx not_active IP Right Cessation
- 1998-01-09 EP EP98904048A patent/EP0956281B1/de not_active Expired - Lifetime
- 1998-01-09 CN CN98801733A patent/CN1125812C/zh not_active Expired - Lifetime
- 1998-01-09 AU AU62081/98A patent/AU730776B2/en not_active Ceased
- 1998-01-09 ID IDW990520A patent/ID22645A/id unknown
- 1998-01-09 AT AT98904048T patent/ATE222235T1/de active
- 1998-01-09 HU HU0000944A patent/HU227625B1/hu active Protection Beyond IP Right Term
- 1998-01-09 PL PL98335647A patent/PL195956B1/pl unknown
- 1998-01-09 RU RU99118590/04A patent/RU2186765C2/ru not_active IP Right Cessation
- 1998-01-09 CZ CZ0250899A patent/CZ301778B6/cs not_active IP Right Cessation
- 1998-01-09 TR TR1999/01674T patent/TR199901674T2/xx unknown
- 1998-01-09 US US09/004,926 patent/US5914425A/en not_active Expired - Lifetime
- 1998-01-09 CA CA2632585A patent/CA2632585C/en not_active Expired - Lifetime
- 1998-01-09 CA CA2634811A patent/CA2634811C/en not_active Expired - Lifetime
- 1998-01-09 DK DK98904048T patent/DK0956281T3/da active
- 1998-01-09 JP JP53362698A patent/JP4138886B2/ja not_active Expired - Lifetime
- 1998-01-09 IL IL13038498A patent/IL130384A/xx not_active IP Right Cessation
- 1998-01-09 ES ES98904048T patent/ES2178152T3/es not_active Expired - Lifetime
- 1998-01-09 DE DE59805186T patent/DE59805186D1/de not_active Expired - Lifetime
- 1998-01-10 EG EG3098A patent/EG21239A/xx active
- 1998-01-15 TW TW087100485A patent/TW531527B/zh not_active IP Right Cessation
- 1998-01-15 ZA ZA9800319A patent/ZA98319B/xx unknown
- 1998-01-20 AR ARP980100249A patent/AR015349A1/es active IP Right Grant
- 1998-09-01 UA UA99084740A patent/UA63937C2/uk unknown
- 1998-10-29 US US09/181,671 patent/US6538151B1/en not_active Expired - Lifetime
-
1999
- 1999-06-29 IS IS5098A patent/IS2115B/is unknown
- 1999-07-13 NO NO19993452A patent/NO311642B1/no not_active IP Right Cessation
- 1999-08-10 BG BG103657A patent/BG63893B1/bg unknown
-
2011
- 2011-09-16 NO NO2011017C patent/NO2011017I2/no unknown
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