HRP20161429T1 - Farmaceutski sastav - Google Patents
Farmaceutski sastav Download PDFInfo
- Publication number
- HRP20161429T1 HRP20161429T1 HRP20161429TT HRP20161429T HRP20161429T1 HR P20161429 T1 HRP20161429 T1 HR P20161429T1 HR P20161429T T HRP20161429T T HR P20161429TT HR P20161429 T HRP20161429 T HR P20161429T HR P20161429 T1 HRP20161429 T1 HR P20161429T1
- Authority
- HR
- Croatia
- Prior art keywords
- range
- present
- mass percent
- pharmaceutical composition
- oral pharmaceutical
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 claims 8
- 239000008203 oral pharmaceutical composition Substances 0.000 claims 6
- XNRVGTHNYCNCFF-UHFFFAOYSA-N Lapatinib ditosylate monohydrate Chemical compound O.CC1=CC=C(S(O)(=O)=O)C=C1.CC1=CC=C(S(O)(=O)=O)C=C1.O1C(CNCCS(=O)(=O)C)=CC=C1C1=CC=C(N=CN=C2NC=3C=C(Cl)C(OCC=4C=C(F)C=CC=4)=CC=3)C2=C1 XNRVGTHNYCNCFF-UHFFFAOYSA-N 0.000 claims 5
- 229920000168 Microcrystalline cellulose Polymers 0.000 claims 4
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims 4
- 235000019359 magnesium stearate Nutrition 0.000 claims 4
- 229940016286 microcrystalline cellulose Drugs 0.000 claims 4
- 235000019813 microcrystalline cellulose Nutrition 0.000 claims 4
- 239000008108 microcrystalline cellulose Substances 0.000 claims 4
- 239000000203 mixture Substances 0.000 claims 4
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims 4
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims 4
- 229940069328 povidone Drugs 0.000 claims 4
- 229940079832 sodium starch glycolate Drugs 0.000 claims 4
- 229920003109 sodium starch glycolate Polymers 0.000 claims 4
- 239000008109 sodium starch glycolate Substances 0.000 claims 4
- 239000007888 film coating Substances 0.000 claims 2
- 238000009501 film coating Methods 0.000 claims 2
Classifications
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- 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
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
- A61K47/38—Cellulose; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2013—Organic compounds, e.g. phospholipids, fats
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/2027—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2059—Starch, including chemically or physically modified derivatives; Amylose; Amylopectin; Dextrin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
- A61K9/2806—Coating materials
- A61K9/2833—Organic macromolecular compounds
- A61K9/286—Polysaccharides, e.g. gums; Cyclodextrin
- A61K9/2866—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
Claims (6)
1. Oralni farmaceutski sastav koji predstavlja sastav jezgre tablete, naznačen time, da obuhvaća sljedeće:
(i) N-{3-kloro-4-[(3-fluorobenzil)oksi]fenil}-6-[5-({[2-(metansulfonil)etil]amino}metil)-2-furil]-4-kinazolinamin-ditosilat-monohidrat koji je prisutan u rasponu od 30 do 60 masenih postotaka;
(ii) povidon koji je prisutan u rasponu od 4 do 9 masenih postotaka;
(iii) natrijev škrobni glikolat koji je prisutan u rasponu od 2 do 8 masenih postotaka;
(iv) mikrokristalna celuloza koja je prisutna u rasponu od 35 do 50 masenih postotaka; i
(v) magnezijev stearat koji je prisutan u rasponu od 0,6 do 1,3 masenih postotaka.
2. Oralni farmaceutski sastav prema zahtjevu 1, naznačen time, da:
(i) je navedeni N-{3-kloro-4-[(3-fluorobenzil)oksi]fenil}-6-[5-({[2-(metansulfonil)etil]amino}metil)-2-furil]-4-kinazolinamin-ditosilat-
monohidrat prisutan u rasponu od 42 do 48 masenih postotaka;
(ii) je navedeni povidon prisutan u rasponu od 5,5 do 7,5 masenih postotaka;
(iii) je navedeni natrijev škrobni glikolat prisutan u rasponu od 3,5 do 5,5 masenih postotaka;
(iv) je spomenuta mikrokristalna celuloza prisutna u rasponu od 40 do 46 masenih postotaka; i
(v) je navedeni magnezijev stearat prisutan u rasponu od 0,8 do 1,2 masenih postotaka.
3. Oralni farmaceutski sastav koji predstavlja sastav tablete, naznačen time, da obuhvaća sljedeće:
(i) N-{3-kloro-4-[(3-fluorobenzil)oksi]fenil}-6-[5-({[2-(metansulfonil)etil]amino}metil)-2-furil]-4-kinazolinamin-ditosilat-monohidrat koji je prisutan u rasponu od 30 do 60 masenih postotaka;
(ii) povidon koji je prisutan u rasponu od 4 do 9 masenih postotaka;
(iii) natrijev škrobni glikolat koji je prisutan u rasponu od 2 do 8 masenih postotaka;
(iv) mikrokristalna celuloza koja je prisutna u rasponu od 35 do 50 masenih postotaka;
(v) magnezijev stearat koji je prisutan u rasponu od 0,6 do 1,3 masenih postotaka; i
(vi) obloga filmom koja je prisutna u rasponu od 2,5 do 3,5 masenih postotaka od sastava jezgre tablete.
4. Oralni farmaceutski sastav prema zahtjevu 3, naznačen time, da obuhvaća sljedeće:
(i) N-{3-kloro-4-[(3-fluorobenzil)oksi]fenil}-6-[5-({[2-(metansulfonil)etil]amino}metil)-2-furil]-4-kinazolinamin-ditosilat-monohidrat koji je prisutan u rasponu od 42 do 48 masenih postotaka;
(ii) povidon koji je prisutan u rasponu od 5,5 do 7,5 masenih postotaka;
(iii) natrijev škrobni glikolat koji je prisutan u rasponu od 3,5 do 5,5 masenih postotaka;
(iv) mikrokristalna celuloza koja je prisutna u rasponu od 40 do 46 masenih postotaka;
(v) magnezijev stearat koji je prisutan u rasponu od 0,8 do 1,2 masenih postotaka; i
(vi) obloga filmom koja je prisutna u rasponu od 2,8 do 3,2 masenih postotaka od sastava jezgre tablete.
5. Oralni farmaceutski sastav prema zahtjevu 3, naznačen time, da obuhvaća sljedeće:
N-{3-kloro-4-[(3-fluorobenzil)oksi]fenil}-6-[5-({[2-(metansulfonil)etil]amino}metil)-2-furil]-4-kinazolinamin-ditosilat-monohidrat koji je prisutan u rasponu od 30 do 47 masenih postotaka.
6. Oralni farmaceutski sastav prema bilo kojem od zahtjeva 1 do 5, naznačen time, da se upotrebljava u liječenju.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US67280505P | 2005-04-19 | 2005-04-19 | |
| EP06750475.3A EP1871347B1 (en) | 2005-04-19 | 2006-04-18 | Pharmaceutical composition |
| PCT/US2006/014447 WO2006113649A1 (en) | 2005-04-19 | 2006-04-18 | Pharmaceutical composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HRP20161429T1 true HRP20161429T1 (hr) | 2016-12-16 |
Family
ID=37115487
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HRP20161429TT HRP20161429T1 (hr) | 2005-04-19 | 2016-11-02 | Farmaceutski sastav |
Country Status (28)
| Country | Link |
|---|---|
| US (3) | US8821927B2 (hr) |
| EP (1) | EP1871347B1 (hr) |
| JP (1) | JP5202302B2 (hr) |
| KR (1) | KR101356748B1 (hr) |
| CN (1) | CN101203211B (hr) |
| AR (1) | AR054252A1 (hr) |
| AU (1) | AU2006236423B2 (hr) |
| BR (1) | BRPI0609962B1 (hr) |
| CA (1) | CA2606207C (hr) |
| CY (1) | CY1118179T1 (hr) |
| DK (1) | DK1871347T3 (hr) |
| EA (1) | EA200702253A1 (hr) |
| ES (1) | ES2601503T3 (hr) |
| HR (1) | HRP20161429T1 (hr) |
| HU (1) | HUE030982T2 (hr) |
| IL (1) | IL186336A0 (hr) |
| LT (1) | LT1871347T (hr) |
| MA (1) | MA29404B1 (hr) |
| MX (1) | MX2007013089A (hr) |
| NO (1) | NO20075111L (hr) |
| NZ (1) | NZ562223A (hr) |
| PE (1) | PE20061430A1 (hr) |
| PL (1) | PL1871347T3 (hr) |
| PT (1) | PT1871347T (hr) |
| SI (1) | SI1871347T1 (hr) |
| TW (1) | TW200716204A (hr) |
| WO (1) | WO2006113649A1 (hr) |
| ZA (1) | ZA200708705B (hr) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200716204A (en) * | 2005-04-19 | 2007-05-01 | Smithkline Beecham Cork Ltd | Pharmaceutical composition |
| WO2009137714A2 (en) * | 2008-05-07 | 2009-11-12 | Teva Pharmaceutical Industries Ltd. | Forms of lapatinib ditosylate and processes for preparation thereof |
| EP2158912A1 (en) * | 2008-08-25 | 2010-03-03 | Ratiopharm GmbH | Pharmaceutical composition comprising N-[3-chhloro-4-[3-fluorophenyl)methoxy)phenyl]6-[5[[[2-(methylsulfonyl)ethyl]amino]methyl]-2-furyl]-4-quinazolinamine |
| EP2158913A1 (en) | 2008-08-25 | 2010-03-03 | Ratiopharm GmbH | Pharmaceutical composition comprising N-[3-chhloro-4-[(3-fluorophenyl)methoxy]phenyl]6-(5[[[2-(methylsulfonyl)ethyl]amino]methyl]-2-furyl]-4-quinazolinamine |
| WO2010099150A1 (en) * | 2009-02-24 | 2010-09-02 | Smithkline Beecham (Cork) Limited | Pharmaceutical tablet and process |
| US20120245351A1 (en) * | 2009-09-29 | 2012-09-27 | Natco Pharma Limited | Process for the preparation of lapatinib and its pharmaceutically acceptable salts |
| WO2011146710A1 (en) | 2010-05-21 | 2011-11-24 | Glaxosmithkline Llc | Combination |
| US9180129B2 (en) | 2010-05-21 | 2015-11-10 | Novartis Ag | Combination of lapatinib and trametinib |
| US9907767B2 (en) | 2010-08-03 | 2018-03-06 | Velicept Therapeutics, Inc. | Pharmaceutical compositions and the treatment of overactive bladder |
| AU2011285928B9 (en) | 2010-08-03 | 2018-08-02 | B3Ar Therapeutics, Inc. | Combinations of beta - 3 adrenergic receptor agonists and muscarinic receptor antagonists for treating overactive bladder |
| WO2014128107A1 (en) | 2013-02-19 | 2014-08-28 | Hexal Ag | Pharmaceutical composition comprising n-[3-chloro-4-(3-fluorobenzyloxy)phenyl]-6-[5({[2-(methylsulfonyl)ethyl]amino}methyl)-2-furyl]quinazolin-4-amine or a pharmaceutically acceptable salt, solvate or solvated salt thereof |
| WO2014170910A1 (en) | 2013-04-04 | 2014-10-23 | Natco Pharma Limited | Process for the preparation of lapatinib |
| US9636340B2 (en) | 2013-11-12 | 2017-05-02 | Ayyappan K. Rajasekaran | Kinase inhibitors |
| KR20170086659A (ko) | 2014-12-03 | 2017-07-26 | 벨리셉트 테라퓨틱스, 인크. | 하부 요로 증상을 위한 변형 방출형 솔라베그론을 이용한 조성물 및 방법 |
| CN106389373B (zh) * | 2015-07-29 | 2019-07-02 | 四川科伦药物研究院有限公司 | 一种二甲苯磺酸拉帕替尼片剂及其制备方法 |
| CN106511289A (zh) * | 2015-09-10 | 2017-03-22 | 湖北生物医药产业技术研究院有限公司 | 甲苯磺酸拉帕替尼片剂及其制备方法 |
| IL310527A (en) | 2015-10-23 | 2024-03-01 | B3Ar Therapeutics Inc | Zwitterion solvegron and its uses |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5506248A (en) * | 1993-08-02 | 1996-04-09 | Bristol-Myers Squibb Company | Pharmaceutical compositions having good dissolution properties |
| GB9508538D0 (en) | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quinazoline derivatives |
| US5760041A (en) | 1996-02-05 | 1998-06-02 | American Cyanamid Company | 4-aminoquinazoline EGFR Inhibitors |
| CA2288140C (en) | 1997-04-25 | 2007-04-03 | Janssen Pharmaceutica N.V. | Farnesyltransferase inhibiting quinazolinones |
| TW436485B (en) | 1997-08-01 | 2001-05-28 | American Cyanamid Co | Substituted quinazoline derivatives |
| RS49779B (sr) | 1998-01-12 | 2008-06-05 | Glaxo Group Limited, | Biciklična heteroaromatična jedinjenja kao inhibitori protein tirozin kinaze |
| CN1305872C (zh) | 2000-06-30 | 2007-03-21 | 葛兰素集团有限公司 | 喹唑啉类化合物的制备方法 |
| AU2002236765A1 (en) | 2001-01-16 | 2002-07-30 | Glaxo Group Limited | Pharmaceutical combination for the treatment of cancer containing a 4-quinazolineamine and another anti-neoplastic agent |
| US20050176740A1 (en) | 2002-04-08 | 2005-08-11 | Spector Neil L. | Cancer treatment method comprising administering an erb-family inhibitor and a raf and/or ras inhibitor |
| EP1810034A4 (en) | 2002-06-19 | 2008-06-25 | Smithkline Beecham Corp | PREDICTIVE MARKERS IN CANCER THERAPY |
| TW200716204A (en) * | 2005-04-19 | 2007-05-01 | Smithkline Beecham Cork Ltd | Pharmaceutical composition |
-
2006
- 2006-04-18 TW TW095113811A patent/TW200716204A/zh unknown
- 2006-04-18 ES ES06750475.3T patent/ES2601503T3/es active Active
- 2006-04-18 SI SI200632109A patent/SI1871347T1/sl unknown
- 2006-04-18 EP EP06750475.3A patent/EP1871347B1/en active Active
- 2006-04-18 DK DK06750475.3T patent/DK1871347T3/en active
- 2006-04-18 KR KR1020077026740A patent/KR101356748B1/ko active IP Right Grant
- 2006-04-18 LT LTEP06750475.3T patent/LT1871347T/lt unknown
- 2006-04-18 WO PCT/US2006/014447 patent/WO2006113649A1/en active Application Filing
- 2006-04-18 US US11/911,843 patent/US8821927B2/en active Active
- 2006-04-18 EA EA200702253A patent/EA200702253A1/ru unknown
- 2006-04-18 BR BRPI0609962-9A patent/BRPI0609962B1/pt active IP Right Grant
- 2006-04-18 JP JP2008507783A patent/JP5202302B2/ja active Active
- 2006-04-18 NZ NZ562223A patent/NZ562223A/en not_active IP Right Cessation
- 2006-04-18 AR AR20060101526A patent/AR054252A1/es not_active Application Discontinuation
- 2006-04-18 PL PL06750475T patent/PL1871347T3/pl unknown
- 2006-04-18 PT PT67504753T patent/PT1871347T/pt unknown
- 2006-04-18 PE PE2006000406A patent/PE20061430A1/es not_active Application Discontinuation
- 2006-04-18 CA CA2606207A patent/CA2606207C/en active Active
- 2006-04-18 AU AU2006236423A patent/AU2006236423B2/en not_active Revoked
- 2006-04-18 HU HUE06750475A patent/HUE030982T2/en unknown
- 2006-04-18 CN CN2006800219417A patent/CN101203211B/zh active Active
- 2006-04-18 MX MX2007013089A patent/MX2007013089A/es active IP Right Grant
-
2007
- 2007-10-07 IL IL186336A patent/IL186336A0/en unknown
- 2007-10-09 NO NO20075111A patent/NO20075111L/no not_active Application Discontinuation
- 2007-10-11 ZA ZA200708705A patent/ZA200708705B/xx unknown
- 2007-10-25 MA MA30318A patent/MA29404B1/fr unknown
-
2014
- 2014-07-28 US US14/444,637 patent/US20140335177A1/en not_active Abandoned
-
2016
- 2016-01-29 US US15/009,927 patent/US20160143909A1/en not_active Abandoned
- 2016-11-02 HR HRP20161429TT patent/HRP20161429T1/hr unknown
- 2016-11-03 CY CY20161101115T patent/CY1118179T1/el unknown
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