NL1008139C2 - Antimicrobiële peptiden. - Google Patents
Antimicrobiële peptiden. Download PDFInfo
- Publication number
- NL1008139C2 NL1008139C2 NL1008139A NL1008139A NL1008139C2 NL 1008139 C2 NL1008139 C2 NL 1008139C2 NL 1008139 A NL1008139 A NL 1008139A NL 1008139 A NL1008139 A NL 1008139A NL 1008139 C2 NL1008139 C2 NL 1008139C2
- Authority
- NL
- Netherlands
- Prior art keywords
- amino acids
- peptide
- peptides according
- domain
- amino acid
- Prior art date
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- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 1
- 240000000968 Parkia biglobosa Species 0.000 description 1
- 241000235645 Pichia kudriavzevii Species 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 241001135221 Prevotella intermedia Species 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 241000589516 Pseudomonas Species 0.000 description 1
- 241000589517 Pseudomonas aeruginosa Species 0.000 description 1
- 102000018968 Salivary Cystatins Human genes 0.000 description 1
- 108010026774 Salivary Cystatins Proteins 0.000 description 1
- 102000001848 Salivary Proteins and Peptides Human genes 0.000 description 1
- 108010029987 Salivary Proteins and Peptides Proteins 0.000 description 1
- 241000607142 Salmonella Species 0.000 description 1
- 241000293869 Salmonella enterica subsp. enterica serovar Typhimurium Species 0.000 description 1
- 241000191940 Staphylococcus Species 0.000 description 1
- 108010059993 Vancomycin Proteins 0.000 description 1
- 241000607734 Yersinia <bacteria> Species 0.000 description 1
- 241000607447 Yersinia enterocolitica Species 0.000 description 1
- 230000009435 amidation Effects 0.000 description 1
- 238000007112 amidation reaction Methods 0.000 description 1
- 229940009444 amphotericin Drugs 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000000843 anti-fungal effect Effects 0.000 description 1
- 230000001857 anti-mycotic effect Effects 0.000 description 1
- 230000000656 anti-yeast Effects 0.000 description 1
- 238000011482 antibacterial activity assay Methods 0.000 description 1
- 102000036639 antigens Human genes 0.000 description 1
- 108091007433 antigens Proteins 0.000 description 1
- 239000002543 antimycotic Substances 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- 208000032343 candida glabrata infection Diseases 0.000 description 1
- 229940055022 candida parapsilosis Drugs 0.000 description 1
- 150000001718 carbodiimides Chemical class 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 125000000151 cysteine group Chemical group N[C@@H](CS)C(=O)* 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 210000003743 erythrocyte Anatomy 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 229960003692 gamma aminobutyric acid Drugs 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 230000009036 growth inhibition Effects 0.000 description 1
- 230000002949 hemolytic effect Effects 0.000 description 1
- 229910052588 hydroxylapatite Inorganic materials 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000002054 inoculum Substances 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229960003085 meticillin Drugs 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- XYJRXVWERLGGKC-UHFFFAOYSA-D pentacalcium;hydroxide;triphosphate Chemical compound [OH-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O XYJRXVWERLGGKC-UHFFFAOYSA-D 0.000 description 1
- 238000010647 peptide synthesis reaction Methods 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 108010005636 polypeptide C Proteins 0.000 description 1
- 239000003910 polypeptide antibiotic agent Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 238000004007 reversed phase HPLC Methods 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000002798 spectrophotometry method Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- HNKJADCVZUBCPG-UHFFFAOYSA-N thioanisole Chemical compound CSC1=CC=CC=C1 HNKJADCVZUBCPG-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 239000001974 tryptic soy broth Substances 0.000 description 1
- 108010050327 trypticase-soy broth Proteins 0.000 description 1
- 229960003165 vancomycin Drugs 0.000 description 1
- MYPYJXKWCTUITO-LYRMYLQWSA-N vancomycin Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=C2C=C3C=C1OC1=CC=C(C=C1Cl)[C@@H](O)[C@H](C(N[C@@H](CC(N)=O)C(=O)N[C@H]3C(=O)N[C@H]1C(=O)N[C@H](C(N[C@@H](C3=CC(O)=CC(O)=C3C=3C(O)=CC=C1C=3)C(O)=O)=O)[C@H](O)C1=CC=C(C(=C1)Cl)O2)=O)NC(=O)[C@@H](CC(C)C)NC)[C@H]1C[C@](C)(N)[C@H](O)[C@H](C)O1 MYPYJXKWCTUITO-LYRMYLQWSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229940098232 yersinia enterocolitica Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/08—Linear peptides containing only normal peptide links having 12 to 20 amino acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
- C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
- C07K14/4723—Cationic antimicrobial peptides, e.g. defensins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Biochemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Communicable Diseases (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Toxicology (AREA)
- Zoology (AREA)
- Gastroenterology & Hepatology (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicinal Preparation (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL1008139A NL1008139C2 (nl) | 1998-01-27 | 1998-01-27 | Antimicrobiële peptiden. |
| CA002319094A CA2319094C (fr) | 1998-01-27 | 1999-01-26 | Peptides antimicrobiens |
| JP2000528598A JP2003524578A (ja) | 1998-01-27 | 1999-01-26 | 抗微生物性ペプチド |
| AT99902926T ATE278710T1 (de) | 1998-01-27 | 1999-01-26 | Antimikrobiell wirksame peptide |
| PCT/NL1999/000045 WO1999037678A2 (fr) | 1998-01-27 | 1999-01-26 | Peptides antimicrobiens |
| US09/601,124 US6638531B1 (en) | 1998-01-27 | 1999-01-26 | Antimicrobial peptides |
| EP99902926A EP1051433B1 (fr) | 1998-01-27 | 1999-01-26 | Peptides antimicrobiens |
| AU23014/99A AU759026B2 (en) | 1998-01-27 | 1999-01-26 | Antimicrobial peptides |
| ES99902926T ES2229669T3 (es) | 1998-01-27 | 1999-01-26 | Peptidos antimicrobianos. |
| DE69920877T DE69920877T2 (de) | 1998-01-27 | 1999-01-26 | Antimikrobiell wirksame peptide |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL1008139 | 1998-01-27 | ||
| NL1008139A NL1008139C2 (nl) | 1998-01-27 | 1998-01-27 | Antimicrobiële peptiden. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NL1008139C2 true NL1008139C2 (nl) | 1999-07-28 |
Family
ID=19766423
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL1008139A NL1008139C2 (nl) | 1998-01-27 | 1998-01-27 | Antimicrobiële peptiden. |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US6638531B1 (fr) |
| EP (1) | EP1051433B1 (fr) |
| JP (1) | JP2003524578A (fr) |
| AT (1) | ATE278710T1 (fr) |
| AU (1) | AU759026B2 (fr) |
| CA (1) | CA2319094C (fr) |
| DE (1) | DE69920877T2 (fr) |
| ES (1) | ES2229669T3 (fr) |
| NL (1) | NL1008139C2 (fr) |
| WO (1) | WO1999037678A2 (fr) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000001427A1 (fr) * | 1998-07-02 | 2000-01-13 | Stichting Skeletal Tissue Engineering Group Amsterdam | Ciment a base d'os, contenant des peptides antimicrobiens |
| NL1010692C2 (nl) * | 1998-12-01 | 2000-06-06 | Stichting Tech Wetenschapp | Antivirale peptiden. |
| EP1174027A1 (fr) * | 2000-07-17 | 2002-01-23 | HOM Consultancy B.V. | Utilisations de peptides antimicrobiens |
| US7550558B2 (en) * | 2001-06-01 | 2009-06-23 | Fundacao De Ampara A Pesquiso Do Estado De Sao Paolo (Fapesp) | Antimicrobial peptides and methods for identifying and using such peptides |
| US7550430B2 (en) * | 2003-08-18 | 2009-06-23 | E.I. Du Pont De Nemours And Company | Cationic antimicrobial peptides and compositions |
| JP2005350424A (ja) * | 2004-06-14 | 2005-12-22 | Kyocera Chemical Corp | 固形製剤および固形製剤の製造方法 |
| EP3384938A1 (fr) | 2011-09-12 | 2018-10-10 | Moderna Therapeutics, Inc. | Acides nucléiques techniques et leurs procédés d'utilisation |
| AU2013243949A1 (en) | 2012-04-02 | 2014-10-30 | Moderna Therapeutics, Inc. | Modified polynucleotides for the production of biologics and proteins associated with human disease |
| EP2833923A4 (fr) | 2012-04-02 | 2016-02-24 | Moderna Therapeutics Inc | Polynucléotides modifiés pour la production de protéines |
| US8963676B1 (en) * | 2013-03-12 | 2015-02-24 | XP Power Limited | Configurable transformer module |
| WO2014144004A1 (fr) | 2013-03-15 | 2014-09-18 | The Board Of Trustees Of The University Of Arkansas | Peptides ayant une activité antifongique et procédés d'utilisation des peptides |
| EP3423477B1 (fr) | 2015-06-30 | 2021-09-29 | Chain Antimicrobials OY | Nouveaux peptides antimicrobiens, leurs variants et leurs utilisations |
| WO2017001732A1 (fr) | 2015-06-30 | 2017-01-05 | Oulun Yliopisto | Nouveaux peptides antimicrobiens, leurs variants et leurs utilisations |
| ES2808780T3 (es) | 2015-06-30 | 2021-03-01 | Chain Antimicrobials Oy | Nuevos péptidos antimicrobianos, sus variantes y usos |
| KR20180101341A (ko) | 2015-11-10 | 2018-09-12 | 비스테라, 인크. | 리포폴리사카라이드에 특이적으로 결합하는 항체 분자-약물 접합체 및 그의 용도 |
| JP6658265B2 (ja) * | 2016-04-26 | 2020-03-04 | ライオン株式会社 | インビトロバイオフィルムモデルの製造方法、ならびに評価方法及び口腔用組成物を選定する方法 |
| EP3571223B1 (fr) | 2017-01-18 | 2024-09-18 | Visterra, Inc. | Conjugués molécule d'anticorps-médicament et leurs utilisations |
| EP3737750B1 (fr) | 2018-01-09 | 2024-06-05 | Theriva Biologics, Inc. | Agents de phosphatase alcaline pour le traitement de troubles neurodéveloppementaux |
| EP3768302A4 (fr) | 2018-03-20 | 2021-12-15 | Synthetic Biologics, Inc. | Formulations de phosphatase alcaline intestinale |
| EP3773686B1 (fr) | 2018-03-20 | 2023-06-07 | Theriva Biologics, Inc. | Agents au phosphatase alcaline pour le traitement de troubles dus à une exposition à des radiations |
| JP2023521319A (ja) | 2020-04-03 | 2023-05-24 | ビステラ， インコーポレイテッド | 抗体分子－薬物コンジュゲートおよびその使用 |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1991012815A1 (fr) * | 1990-02-23 | 1991-09-05 | Bristol-Myers Squibb Company | COMPOSITIONS ET PROCEDES POUR TRAITER DES INFECTIONS CAUSEES PAR DES ORGANISMES SENSIBLES AUX ANTIBIOTIQUES β-LACTAME |
| WO1992001462A1 (fr) * | 1990-07-19 | 1992-02-06 | The Scripps Research Institute | Compositions de peptides amphiphiles et analogues de ces compositions |
| WO1993024138A1 (fr) * | 1992-06-01 | 1993-12-09 | Magainin Pharmaceuticals, Inc. | Peptides biologiquement actifs presentant des substitutions n-terminales |
| WO1996008270A2 (fr) * | 1994-09-13 | 1996-03-21 | Magainin Pharmaceuticals Inc. | Procede permettant d'inhiber la transmission de maladies sexuellement transmissibles a l'aide d'antimicrobiens du type magainin ou de composes de squalamine |
| WO1996040251A1 (fr) * | 1995-06-07 | 1996-12-19 | Ophidian Pharmaceuticals, Inc. | Prevention et traitement de la septicemie |
-
1998
- 1998-01-27 NL NL1008139A patent/NL1008139C2/nl not_active IP Right Cessation
-
1999
- 1999-01-26 AU AU23014/99A patent/AU759026B2/en not_active Ceased
- 1999-01-26 CA CA002319094A patent/CA2319094C/fr not_active Expired - Fee Related
- 1999-01-26 DE DE69920877T patent/DE69920877T2/de not_active Expired - Fee Related
- 1999-01-26 WO PCT/NL1999/000045 patent/WO1999037678A2/fr active IP Right Grant
- 1999-01-26 US US09/601,124 patent/US6638531B1/en not_active Expired - Fee Related
- 1999-01-26 AT AT99902926T patent/ATE278710T1/de not_active IP Right Cessation
- 1999-01-26 ES ES99902926T patent/ES2229669T3/es not_active Expired - Lifetime
- 1999-01-26 JP JP2000528598A patent/JP2003524578A/ja active Pending
- 1999-01-26 EP EP99902926A patent/EP1051433B1/fr not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1991012815A1 (fr) * | 1990-02-23 | 1991-09-05 | Bristol-Myers Squibb Company | COMPOSITIONS ET PROCEDES POUR TRAITER DES INFECTIONS CAUSEES PAR DES ORGANISMES SENSIBLES AUX ANTIBIOTIQUES β-LACTAME |
| WO1992001462A1 (fr) * | 1990-07-19 | 1992-02-06 | The Scripps Research Institute | Compositions de peptides amphiphiles et analogues de ces compositions |
| WO1993024138A1 (fr) * | 1992-06-01 | 1993-12-09 | Magainin Pharmaceuticals, Inc. | Peptides biologiquement actifs presentant des substitutions n-terminales |
| WO1996008270A2 (fr) * | 1994-09-13 | 1996-03-21 | Magainin Pharmaceuticals Inc. | Procede permettant d'inhiber la transmission de maladies sexuellement transmissibles a l'aide d'antimicrobiens du type magainin ou de composes de squalamine |
| WO1996040251A1 (fr) * | 1995-06-07 | 1996-12-19 | Ophidian Pharmaceuticals, Inc. | Prevention et traitement de la septicemie |
Non-Patent Citations (8)
| Title |
|---|
| AOYAGI H ET AL: "SYNTHESIS OF ANTIBACTERIAL PEPTIDES, GRAMICIDIN S ANALOGS AND DESIGNED AMPHIPHILIC OLIGOPEPTIDES", TETRAHEDRON, vol. 44, no. 3, 1 January 1988 (1988-01-01), pages 877 - 886, XP000574054 * |
| CHEMICAL ABSTRACTS, vol. 103, no. 19, 11 November 1985, Columbus, Ohio, US; abstract no. 160837, SASAKI, TOORU ET AL: "Syntheses and properties of H-[Orn-Leu]n-OH (n = 1-12) and cyclo[Orn-Leu-]n (n = 2-8)" XP002083173 * |
| CHEMICAL ABSTRACTS, vol. 106, no. 25, 22 June 1987, Columbus, Ohio, US; abstract no. 214352, MIHARA, HISAKAZU ET AL: "Design and synthesis of basic amphiphilic peptides possessing antimicrobial activity and their interaction with lipids" XP002083172 * |
| MIHARA, HISAKAZU ET AL: "Design and synthesis of amphiphilic basic peptides with antibacterial activity and their interaction with model membrane", BULL. CHEM. SOC. JPN. (1987), 60(2), 697-706 CODEN: BCSJA8;ISSN: 0009-2673, 1987, XP002083171 * |
| PEPT. CHEM. (1985), VOLUME DATE 1984, 22ND, 361-6 CODEN: PECHDP;ISSN: 0388-3698, 1985 * |
| PEPT. CHEM. (1986), VOLUME DATE 1985, 23RD, 223-8 CODEN: PECHDP;ISSN: 0388-3698, 1986 * |
| TAKAHASHI, SHO ET AL: "Synthesis of.alpha.-helices having a positively charged random coil-block on either N- or C-terminal", BULL. CHEM. SOC. JPN. (1988), 61(7), 2467-71 CODEN: BCSJA8;ISSN: 0009-2673, 1988, XP002083167 * |
| TOSSI, ALESSANDRO ET AL: "Identification and characterization of a primary antibacterial domain in CAP18, a lipopolysaccharide binding protein from rabbit leukocytes", FEBS LETT. (1994), 339(1-2), 108-12 CODEN: FEBLAL;ISSN: 0014-5793, 1994, XP002083170 * |
Also Published As
| Publication number | Publication date |
|---|---|
| ES2229669T3 (es) | 2005-04-16 |
| EP1051433B1 (fr) | 2004-10-06 |
| AU2301499A (en) | 1999-08-09 |
| WO1999037678A3 (fr) | 1999-10-14 |
| ATE278710T1 (de) | 2004-10-15 |
| CA2319094C (fr) | 2009-03-17 |
| AU759026B2 (en) | 2003-04-03 |
| EP1051433A2 (fr) | 2000-11-15 |
| JP2003524578A (ja) | 2003-08-19 |
| US6638531B1 (en) | 2003-10-28 |
| DE69920877D1 (de) | 2004-11-11 |
| WO1999037678A2 (fr) | 1999-07-29 |
| CA2319094A1 (fr) | 1999-07-29 |
| DE69920877T2 (de) | 2005-02-03 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| SD | Assignments of patents |
Owner name: AM-PHARMA B.V. |
|
| VD1 | Lapsed due to non-payment of the annual fee |
Effective date: 20040801 |