WO1996024370B1 - Pharmaceutical non inorganic saline solutions for endonasal administration of a calcitonin - Google Patents
Pharmaceutical non inorganic saline solutions for endonasal administration of a calcitoninInfo
- Publication number
- WO1996024370B1 WO1996024370B1 PCT/EP1996/000446 EP9600446W WO9624370B1 WO 1996024370 B1 WO1996024370 B1 WO 1996024370B1 EP 9600446 W EP9600446 W EP 9600446W WO 9624370 B1 WO9624370 B1 WO 9624370B1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- calcitonin
- pharmaceutical
- saline solutions
- glucamine
- carbacalcitonin
- Prior art date
Links
- BBBFJLBPOGFECG-VJVYQDLKSA-N calcitonin Chemical compound N([C@H](C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)NCC(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H]([C@@H](C)O)C(=O)N1[C@@H](CCC1)C(N)=O)C(C)C)C(=O)[C@@H]1CSSC[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)O)C(=O)N1 BBBFJLBPOGFECG-VJVYQDLKSA-N 0.000 title claims abstract 6
- 239000011780 sodium chloride Substances 0.000 title claims abstract 6
- 108060001064 Calcitonin Proteins 0.000 title claims abstract 4
- 229960004015 Calcitonin Drugs 0.000 title claims abstract 4
- 102400000113 Calcitonin Human genes 0.000 title claims abstract 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 title claims abstract 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims abstract 6
- JYSJVJJVLNYRKL-QPHHPWFVSA-N Elcatonin Chemical compound N([C@H](C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)NCC(=O)N[C@@H](C)C(=O)NCC(=O)N[C@@H]([C@@H](C)O)C(=O)N1[C@@H](CCC1)C(N)=O)C(C)C)C(=O)C1CCCCCC(=O)OC[C@H](N)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)O)C(=O)N1 JYSJVJJVLNYRKL-QPHHPWFVSA-N 0.000 claims abstract 3
- 229960000756 Elcatonin Drugs 0.000 claims abstract 3
- 150000003839 salts Chemical class 0.000 claims abstract 3
- LENZDBCJOHFCAS-UHFFFAOYSA-N 2-amino-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 claims abstract 2
- 241000972773 Aulopiformes Species 0.000 claims abstract 2
- MBBZMMPHUWSWHV-BDVNFPICSA-N Meglumine Chemical compound CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO MBBZMMPHUWSWHV-BDVNFPICSA-N 0.000 claims abstract 2
- 229940035504 Tromethamine Drugs 0.000 claims abstract 2
- 239000008012 organic excipient Substances 0.000 claims abstract 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims abstract 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims abstract 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims abstract 2
- 235000019515 salmon Nutrition 0.000 claims abstract 2
- 229960000281 trometamol Drugs 0.000 claims abstract 2
- 239000003186 pharmaceutical solution Substances 0.000 claims 3
- HNJBEVLQSNELDL-UHFFFAOYSA-N 2-Pyrrolidone Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims 1
- FMPTWBWKJAJGSR-LJNLPFSOSA-N Calcitare Chemical compound C([C@@H](C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CCSC)C(=O)NCC(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)NCC(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N1[C@@H](CCC1)C(N)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC=1NC=NC=1)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CS)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CS)[C@@H](C)O)C(C)C)C1=CC=CC=C1 FMPTWBWKJAJGSR-LJNLPFSOSA-N 0.000 claims 1
- VSHJAJRPRRNBEK-LMVCGNDWSA-N Eel calcitonin Chemical compound C([C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)CNC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CS)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CS)[C@@H](C)O)C(C)C)CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)NCC(=O)N[C@@H](C)C(=O)NCC(=O)N[C@@H]([C@@H](C)O)C(=O)N1[C@@H](CCC1)C(N)=O)C1=CN=CN1 VSHJAJRPRRNBEK-LMVCGNDWSA-N 0.000 claims 1
- 241000287828 Gallus gallus Species 0.000 claims 1
- 229940045644 Human calcitonin Drugs 0.000 claims 1
- 101500011263 human Calcitonin Proteins 0.000 claims 1
- 239000000243 solution Substances 0.000 claims 1
- 229920002554 vinyl polymer Polymers 0.000 claims 1
- 239000007857 degradation product Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
Abstract
The subject-matter of the invention are pharmaceutical non inorganic saline solutions for endonasal administration containing: (a) a calcitonin, preferably salmon or alternatively carbacalcitonin (elcatonin), or its pharmaceutically acceptable salts; characterized in that it further contains the organic excipients; (b) N-(methyl)-glucamine or glucamine; (c) tromethamine; (d) citric acid; and (e) polyvinylpyrrolidone ranging from K15 to K120. These are odourless and tasteless and thus have improved patient's compliance not having the undesirable secondary effects of known compositions as well as permit a complete and accurate analysis of the activeprinciple and develop less degradation products during storage.
Claims
1. Pharmaceutical non inorganic saline solutions for endonasal administration comprising a) a natural or modified calcitonin, preferably salmon or alternatively carbacalcitonin (elcatonin) , or its pharmaceutically acceptable salts, characterized in that it further comprises the following organic excipients
b) N-(methyl) -glucamine c) tromethamine, d) citric acid, and e) polyvinylpyrrolidone ranging from K15 to
K120 (linear and water-soluble) .
2. Pharmaceutical solutions according to claim 1, characterized in that the calcitonin is human calcitonin, eel calcitonin, carbacalcitonin (elcatonin) , chicken calcitonin or porcine calcitonin.
3. Pharmaceutical solutions according to claim 1 or claim 2, characterized in that the polyvinyl¬ pyrrolidone is of the type K40.
4. Pharmaceutical solutions according to any one of claims 1 to 3 , characterized in that they comprise:
a) the natural or modified calcitonin or its pharmaceutically acceptable salts in concentrations of 250 I.U./ml to 5.000 I.U./ml,
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP96903969A EP0809512B1 (en) | 1995-02-08 | 1996-02-08 | Pharmaceutical non inorganic saline solutions for endonasal administration of a calcitonin |
| AU47863/96A AU4786396A (en) | 1995-02-08 | 1996-02-08 | Pharmaceutical non inorganic saline solutions for endonasal administration of a calcitonin |
| AT96903969T ATE215381T1 (en) | 1995-02-08 | 1996-02-08 | PHARMACEUTICAL NON-INORGANIC SALINE SOLUTIONS FOR ENDONASAL ADMINISTRATION OF A CALCITONIN |
| DE69620393T DE69620393T2 (en) | 1995-02-08 | 1996-02-08 | PHARMACEUTICAL NON-INORGANIC SALT SOLUTIONS FOR ENDONASAL ADMINISTRATION OF A CALCITONIN |
| BR9607410A BR9607410A (en) | 1995-02-08 | 1996-02-08 | Non-inorganic saline pharmaceutical solutions for endonasal administration |
| US08/908,986 US6087338A (en) | 1995-02-08 | 1997-08-08 | Pharmaceutical non inorganic saline solutions for endonasal administration of a calcitonin |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP95101681A EP0726075A1 (en) | 1995-02-08 | 1995-02-08 | Pharmaceutical non-inorganic saline solutions for endonasal administration |
| EP95101681.5 | 1995-02-08 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US08/908,986 Continuation US6087338A (en) | 1995-02-08 | 1997-08-08 | Pharmaceutical non inorganic saline solutions for endonasal administration of a calcitonin |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO1996024370A1 WO1996024370A1 (en) | 1996-08-15 |
| WO1996024370B1 true WO1996024370B1 (en) | 1996-09-19 |
Family
ID=8218965
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP1996/000487 WO1996024618A1 (en) | 1995-02-08 | 1996-02-02 | Calcitonin salmon analogues, their preparation, medicinal use and use as analytical agents |
| PCT/EP1996/000446 WO1996024370A1 (en) | 1995-02-08 | 1996-02-08 | Pharmaceutical non inorganic saline solutions for endonasal administration of a calcitonin |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP1996/000487 WO1996024618A1 (en) | 1995-02-08 | 1996-02-02 | Calcitonin salmon analogues, their preparation, medicinal use and use as analytical agents |
Country Status (17)
| Country | Link |
|---|---|
| US (2) | US6107277A (en) |
| EP (3) | EP0726075A1 (en) |
| JP (2) | JPH11506416A (en) |
| KR (2) | KR100430101B1 (en) |
| AT (2) | ATE191719T1 (en) |
| AU (2) | AU4787996A (en) |
| BR (1) | BR9607410A (en) |
| CA (2) | CA2210664A1 (en) |
| DE (4) | DE726075T1 (en) |
| ES (2) | ES2146869T3 (en) |
| GB (1) | GB9523442D0 (en) |
| HU (1) | HUP9600266A3 (en) |
| PE (1) | PE28397A1 (en) |
| PL (1) | PL183398B1 (en) |
| PT (2) | PT809654E (en) |
| WO (2) | WO1996024618A1 (en) |
| ZA (2) | ZA96779B (en) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0726075A1 (en) * | 1995-02-08 | 1996-08-14 | Therapicon Srl | Pharmaceutical non-inorganic saline solutions for endonasal administration |
| US6034064A (en) * | 1995-04-07 | 2000-03-07 | Hoechst Pharmaceuticals & Chemicals K.K. | Peptides and therapeutic agent for autoimmune diseases containing the same |
| DE19653969A1 (en) * | 1996-12-20 | 1998-06-25 | Boehringer Ingelheim Kg | New aqueous pharmaceutical preparation for the production of propellant-free aerosols |
| IT1298780B1 (en) * | 1998-03-24 | 2000-02-02 | Therapicon Srl | Pharmaceutical compositions for parenteral use are based on aqueous solutions of natural or synthetic calcitonine |
| WO2001052937A1 (en) * | 2000-01-24 | 2001-07-26 | Medtronic Minimed, Inc. | Mixed buffer system for stabilizing polypeptide formulations |
| CA2399505C (en) | 2000-02-04 | 2012-01-03 | Unigene Laboratories, Inc. | Nasal calcitonin formulations |
| DE10024451A1 (en) * | 2000-05-18 | 2001-11-29 | Asta Medica Ag | Pharmaceutical dosage form for peptides, process for their preparation and use |
| US6737401B2 (en) | 2001-06-28 | 2004-05-18 | Metronic Minimed, Inc. | Methods of evaluating protein formulation stability and surfactant-stabilized insulin formulations derived therefrom |
| JP4225416B2 (en) * | 2001-06-29 | 2009-02-18 | 旭化成ファーマ株式会社 | Methods for improving the stability of protein formulations |
| ITMI20021684A1 (en) * | 2002-07-29 | 2004-01-29 | Therapicon Srl | PHARMACEUTICAL COMPOSITION OF NASAL PEPTIDE |
| US20090035260A1 (en) * | 2002-07-29 | 2009-02-05 | Therapicon Srl | Enhanced nasal composition of active peptide |
| US7812120B2 (en) | 2003-03-21 | 2010-10-12 | Par Pharmaceutical, Inc. | Nasal calcitonin formulations containing chlorobutanol |
| ITMI20040235A1 (en) * | 2004-02-13 | 2004-05-13 | Therapicon Srl | PHARMACEUTICAL PREPARATION FOR THE ORAL CABLE |
| GB0422644D0 (en) * | 2004-10-12 | 2004-11-10 | Novartis Ag | Organic compounds |
| WO2006106903A1 (en) | 2005-03-31 | 2006-10-12 | Chugai Seiyaku Kabushiki Kaisha | sc(Fv)2 STRUCTURAL ISOMERS |
| KR101367544B1 (en) | 2005-06-10 | 2014-02-26 | 추가이 세이야쿠 가부시키가이샤 | Stabilizer for protein preparation comprising meglumine and use thereof |
| JP5085322B2 (en) | 2005-06-10 | 2012-11-28 | 中外製薬株式会社 | Pharmaceutical composition containing sc (Fv) 2 |
| CN100349611C (en) * | 2005-11-25 | 2007-11-21 | 中国药科大学 | Redfish calcitonin inhalation powder-atomizing agent and preparing method |
| CN102292346B (en) * | 2009-01-22 | 2015-12-02 | 关键生物科学有限公司 | Fat treatment |
| US9533022B2 (en) | 2011-11-02 | 2017-01-03 | KeyBioscience A/S | Peptide analogs for treating diseases and disorders |
| RU2616511C2 (en) | 2011-11-02 | 2017-04-17 | Кибайосайнс Аг | Peptide analogs for treatment of diseases and disorders |
| WO2024189611A1 (en) * | 2023-03-13 | 2024-09-19 | Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd. | Stabilized analogues of calcitonin |
Family Cites Families (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3926938A (en) * | 1974-08-12 | 1975-12-16 | Armour Pharma | Synthesis of salmon calcitonin |
| US4217268A (en) * | 1978-07-20 | 1980-08-12 | Hughes John L | Synthesis of peptides |
| GB2127689B (en) * | 1982-10-05 | 1986-07-09 | Sandoz Ltd | Calcitonin inhalation compositions |
| CH657779A5 (en) * | 1982-10-05 | 1986-09-30 | Sandoz Ag | GALENIC COMPOSITIONS CONTAINING CALCITONIN. |
| JPS59163313A (en) * | 1983-03-09 | 1984-09-14 | Teijin Ltd | Peptide hormone composition for nasal administration |
| US4659804A (en) * | 1984-11-01 | 1987-04-21 | Armour Pharmaceutical Company | (Bis-1,7-S-acetamidomethyl-L-cysteine)salmon calcitonin |
| JPS61267528A (en) * | 1984-11-26 | 1986-11-27 | Yamanouchi Pharmaceut Co Ltd | Transnasal calcitonin agent containing absorbefacient |
| US4622386A (en) * | 1985-03-28 | 1986-11-11 | Armour Pharmaceutical Company | [1,7-di-alanine]calcitonin |
| US4639510A (en) * | 1985-10-04 | 1987-01-27 | Armour Pharmaceutical Company | (1-S-acetamidomethyl cysteine, 7-alanine)calcitonin |
| HUT44794A (en) * | 1985-12-04 | 1988-04-28 | Sandoz Ag | Process for production of calcitonine-derivatives and medical preparatives containing such compounds |
| DE3876022T2 (en) * | 1987-07-08 | 1993-04-22 | Mitsubishi Petrochemical Co | CALCITONIN DERIVATIVES AND THEIR SALTS. |
| US5059587A (en) * | 1987-08-03 | 1991-10-22 | Toyo Jozo Company, Ltd. | Physiologically active peptide composition for nasal administration |
| ES2061688T3 (en) * | 1987-11-13 | 1994-12-16 | Smithkline Beecham Farma | PHARMACEUTICAL COMPOSITIONS THAT INCLUDE A CALCITONINE AND A GLICIRRICINATE AS IMPROVER OF ABSORPTION. |
| US5153308A (en) * | 1988-06-16 | 1992-10-06 | Teijin Limited | S-sulfonated calcitonin derivatives |
| JPH0694851B2 (en) * | 1988-06-27 | 1994-11-24 | 株式会社日立製作所 | Evaporative fuel control device |
| US5026825A (en) * | 1988-09-08 | 1991-06-25 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Intranasal calcitonin formulations |
| JPH02104531A (en) * | 1988-10-14 | 1990-04-17 | Toyo Jozo Co Ltd | Physiologically active peptide composition for nasal application |
| JPH0643339B2 (en) * | 1990-05-25 | 1994-06-08 | 旭化成工業株式会社 | Method for stabilizing calcitonin aqueous solution composition |
| IT1248725B (en) * | 1990-06-12 | 1995-01-26 | Sclavo Spa | PHARMACEUTICAL COMPOSITION POWDER FOR NASAL ADMINISTRATION CONTAINING ESSENTIAL CALCITONIN AND A WATER SOLUBLE EXCIPIENT |
| JPH078806B2 (en) * | 1990-08-16 | 1995-02-01 | 旭化成工業株式会社 | Nasal emulsion containing calcitonin |
| JP3179538B2 (en) * | 1990-12-11 | 2001-06-25 | ノバルティス アクチエンゲゼルシャフト | Aqueous solution of stable human calcitonin |
| IT1244500B (en) * | 1991-03-21 | 1994-07-15 | Pulitzer Italiana | USE OF TROMETAMINE MINERAL SALTS IN PHARMACEUTICAL COMPOSITIONS BASED ON CALCITONIN ADMINISTRABLE BY RECTAL ROUTE IN HUMAN THERAPY |
| IT1251685B (en) * | 1991-10-11 | 1995-05-19 | Isf Spa | PHARMACEUTICAL COMPOSITIONS CONTAINING A CALCITONIN |
| US5571788A (en) * | 1991-12-09 | 1996-11-05 | Ciba-Geigy Corporation | Stable calcitonin pharmaceutical compositions |
| IT1255895B (en) * | 1992-10-20 | 1995-11-17 | Laura Chiodini | PHARMACEUTICAL COMPOSITIONS CONTAINING A CALCITONIN |
| EP0726075A1 (en) * | 1995-02-08 | 1996-08-14 | Therapicon Srl | Pharmaceutical non-inorganic saline solutions for endonasal administration |
-
1995
- 1995-02-08 EP EP95101681A patent/EP0726075A1/en not_active Withdrawn
- 1995-02-08 DE DE0726075T patent/DE726075T1/en active Pending
- 1995-11-15 GB GBGB9523442.3A patent/GB9523442D0/en active Pending
-
1996
- 1996-02-01 ZA ZA96779A patent/ZA96779B/en unknown
- 1996-02-02 EP EP96903997A patent/EP0809654B1/en not_active Expired - Lifetime
- 1996-02-02 JP JP8523975A patent/JPH11506416A/en not_active Ceased
- 1996-02-02 DE DE29622959U patent/DE29622959U1/en not_active Expired - Lifetime
- 1996-02-02 AT AT96903997T patent/ATE191719T1/en not_active IP Right Cessation
- 1996-02-02 AU AU47879/96A patent/AU4787996A/en not_active Abandoned
- 1996-02-02 KR KR1019970705486A patent/KR100430101B1/en not_active IP Right Cessation
- 1996-02-02 PT PT96903997T patent/PT809654E/en unknown
- 1996-02-02 CA CA002210664A patent/CA2210664A1/en not_active Abandoned
- 1996-02-02 ZA ZA96835A patent/ZA96835B/en unknown
- 1996-02-02 ES ES96903997T patent/ES2146869T3/en not_active Expired - Lifetime
- 1996-02-02 DE DE69607749T patent/DE69607749T2/en not_active Expired - Fee Related
- 1996-02-02 WO PCT/EP1996/000487 patent/WO1996024618A1/en active IP Right Grant
- 1996-02-05 KR KR1019960002720A patent/KR100397034B1/en not_active IP Right Cessation
- 1996-02-07 PL PL96312683A patent/PL183398B1/en not_active IP Right Cessation
- 1996-02-07 HU HU9600266A patent/HUP9600266A3/en unknown
- 1996-02-07 JP JP02092496A patent/JP4123309B2/en not_active Expired - Fee Related
- 1996-02-08 DE DE69620393T patent/DE69620393T2/en not_active Expired - Lifetime
- 1996-02-08 AU AU47863/96A patent/AU4786396A/en not_active Abandoned
- 1996-02-08 AT AT96903969T patent/ATE215381T1/en not_active IP Right Cessation
- 1996-02-08 BR BR9607410A patent/BR9607410A/en not_active IP Right Cessation
- 1996-02-08 CA CA002212520A patent/CA2212520A1/en not_active Abandoned
- 1996-02-08 ES ES96903969T patent/ES2173267T3/en not_active Expired - Lifetime
- 1996-02-08 PT PT96903969T patent/PT809512E/en unknown
- 1996-02-08 WO PCT/EP1996/000446 patent/WO1996024370A1/en active IP Right Grant
- 1996-02-08 EP EP96903969A patent/EP0809512B1/en not_active Expired - Lifetime
- 1996-02-08 PE PE1996000091A patent/PE28397A1/en not_active Application Discontinuation
-
1997
- 1997-08-08 US US08/907,602 patent/US6107277A/en not_active Expired - Fee Related
- 1997-08-08 US US08/908,986 patent/US6087338A/en not_active Expired - Fee Related
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