SK287153B6 - Hexahydrofuro[2,3-b]furan-3-yl-N-{3-[(1,3-benzodioxol-5- ylsulfonyl)(izobutyl)amino]1-benzyl-2-hydroxypropyl}karbamát, jeho použitie a farmaceutický prípravok s jeho obsahom - Google Patents
Hexahydrofuro[2,3-b]furan-3-yl-N-{3-[(1,3-benzodioxol-5- ylsulfonyl)(izobutyl)amino]1-benzyl-2-hydroxypropyl}karbamát, jeho použitie a farmaceutický prípravok s jeho obsahom Download PDFInfo
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- SK287153B6 SK287153B6 SK570-2002A SK5702002A SK287153B6 SK 287153 B6 SK287153 B6 SK 287153B6 SK 5702002 A SK5702002 A SK 5702002A SK 287153 B6 SK287153 B6 SK 287153B6
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- compound
- carbamate
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- hiv
- hydroxypropyl
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- JLFNLZLINWHATN-UHFFFAOYSA-N pentaethylene glycol Chemical compound OCCOCCOCCOCCOCCO JLFNLZLINWHATN-UHFFFAOYSA-N 0.000 description 1
- XDRYMKDFEDOLFX-UHFFFAOYSA-N pentamidine Chemical compound C1=CC(C(=N)N)=CC=C1OCCCCCOC1=CC=C(C(N)=N)C=C1 XDRYMKDFEDOLFX-UHFFFAOYSA-N 0.000 description 1
- 229960004448 pentamidine Drugs 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 230000036470 plasma concentration Effects 0.000 description 1
- YIQPUIGJQJDJOS-UHFFFAOYSA-N plerixafor Chemical compound C=1C=C(CN2CCNCCCNCCNCCC2)C=CC=1CN1CCCNCCNCCCNCC1 YIQPUIGJQJDJOS-UHFFFAOYSA-N 0.000 description 1
- 229960002169 plerixafor Drugs 0.000 description 1
- 229920000447 polyanionic polymer Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 235000011009 potassium phosphates Nutrition 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 230000000069 prophylactic effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- WTTIBCHOELPGFK-LBPRGKRZSA-N r82150 Chemical compound C1N(CC=C(C)C)[C@@H](C)CN2C(=S)NC3=CC=CC1=C32 WTTIBCHOELPGFK-LBPRGKRZSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 108010043277 recombinant soluble CD4 Proteins 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000010076 replication Effects 0.000 description 1
- 230000001177 retroviral effect Effects 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 102200042996 rs1057521927 Human genes 0.000 description 1
- 102200156953 rs121964883 Human genes 0.000 description 1
- 102220246449 rs143520192 Human genes 0.000 description 1
- 102220067568 rs202141764 Human genes 0.000 description 1
- 102220014375 rs397517056 Human genes 0.000 description 1
- 102220018603 rs397517057 Human genes 0.000 description 1
- 102200002453 rs55758736 Human genes 0.000 description 1
- 102220053718 rs573489857 Human genes 0.000 description 1
- 238000010956 selective crystallization Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- FIAFUQMPZJWCLV-UHFFFAOYSA-N suramin Chemical compound OS(=O)(=O)C1=CC(S(O)(=O)=O)=C2C(NC(=O)C3=CC=C(C(=C3)NC(=O)C=3C=C(NC(=O)NC=4C=C(C=CC=4)C(=O)NC=4C(=CC=C(C=4)C(=O)NC=4C5=C(C=C(C=C5C(=CC=4)S(O)(=O)=O)S(O)(=O)=O)S(O)(=O)=O)C)C=CC=3)C)=CC=C(S(O)(=O)=O)C2=C1 FIAFUQMPZJWCLV-UHFFFAOYSA-N 0.000 description 1
- 229960005314 suramin Drugs 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- VCMJCVGFSROFHV-WZGZYPNHSA-N tenofovir disoproxil fumarate Chemical compound OC(=O)\C=C\C(O)=O.N1=CN=C2N(C[C@@H](C)OCP(=O)(OCOC(=O)OC(C)C)OCOC(=O)OC(C)C)C=NC2=C1N VCMJCVGFSROFHV-WZGZYPNHSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 229960000838 tipranavir Drugs 0.000 description 1
- NZPXPXAGXYTROM-FYBSXPHGSA-N tipranavir Chemical compound C([C@@]1(CCC)OC(O)=C([C@H](CC)C=2C=C(NS(=O)(=O)C=3N=CC(=CC=3)C(F)(F)F)C=CC=2)C(=O)C1)CC1=CC=CC=C1 NZPXPXAGXYTROM-FYBSXPHGSA-N 0.000 description 1
- 229950011282 tivirapine Drugs 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- DBGVGMSCBYYSLD-UHFFFAOYSA-N tributylstannane Chemical compound CCCC[SnH](CCCC)CCCC DBGVGMSCBYYSLD-UHFFFAOYSA-N 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 230000009385 viral infection Effects 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
-
- 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
-
- 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
- A61P31/12—Antivirals
-
- 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
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- 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
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- Virology (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15785099P | 1999-10-06 | 1999-10-06 | |
| PCT/EP2000/009917 WO2001025240A1 (en) | 1999-10-06 | 2000-10-06 | HEXAHYDROFURO'2,3-B!FURAN-3-YL-N- {3'(1,3-BENZODIOXOL -5- YLSULFONYL) (ISOBUTYL) AMINO! -1-BENZYL-2-HYDROXYPROPYL} CARBAMATE AS RETROVIRAL PROTEASE INHIBITOR |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SK5702002A3 SK5702002A3 (en) | 2003-01-09 |
| SK287153B6 true SK287153B6 (sk) | 2010-01-07 |
Family
ID=22565540
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK570-2002A SK287153B6 (sk) | 1999-10-06 | 2000-10-06 | Hexahydrofuro[2,3-b]furan-3-yl-N-{3-[(1,3-benzodioxol-5- ylsulfonyl)(izobutyl)amino]1-benzyl-2-hydroxypropyl}karbamát, jeho použitie a farmaceutický prípravok s jeho obsahom |
Country Status (25)
| Country | Link |
|---|---|
| US (2) | US6649651B1 (cs) |
| EP (1) | EP1222192B8 (cs) |
| JP (1) | JP4951179B2 (cs) |
| KR (1) | KR100792391B1 (cs) |
| CN (1) | CN1191256C (cs) |
| AP (1) | AP1459A (cs) |
| AT (1) | ATE398623T1 (cs) |
| AU (1) | AU781656B2 (cs) |
| BR (1) | BR0014602A (cs) |
| CA (1) | CA2386850C (cs) |
| CZ (1) | CZ300031B6 (cs) |
| DE (1) | DE60039244D1 (cs) |
| DK (1) | DK1222192T3 (cs) |
| ES (1) | ES2307533T3 (cs) |
| HU (1) | HU228938B1 (cs) |
| IL (2) | IL149005A0 (cs) |
| MX (1) | MXPA02003607A (cs) |
| NO (1) | NO327996B1 (cs) |
| NZ (1) | NZ518580A (cs) |
| OA (1) | OA12053A (cs) |
| PL (1) | PL204924B1 (cs) |
| RU (1) | RU2247123C2 (cs) |
| SK (1) | SK287153B6 (cs) |
| WO (1) | WO2001025240A1 (cs) |
| ZA (1) | ZA200202655B (cs) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CZ300031B6 (cs) * | 1999-10-06 | 2009-01-14 | Tibotec Pharmaceuticals Ltd. | Hexahydrofuro[2,3-b]furan-3-yl-N-{3-[(1,3-benzodioxol-5-ylsulfonyl) (isobutyl)amino]-1-benzyl-2-hydroxypropyl}karbamát a farmaceutický prípravek s jeho obsahem |
| OA12464A (en) * | 2001-04-09 | 2006-05-24 | Tibotec Pharm Ltd | Broadspectrum 2-(substituted-amino)-benzoxazole sulfonamide HIV protease inhibitors. |
| AP1758A (en) * | 2001-09-10 | 2007-07-30 | Tibotec Pharm Ltd | Method for the preparation of hexahydro-furo [2,3-b]furan-3-ol. |
| AU2003202914A1 (en) * | 2002-01-07 | 2003-07-24 | Sequoia Pharmaceuticals | Broad spectrum inhibitors |
| US7285566B2 (en) * | 2002-01-07 | 2007-10-23 | Erickson John W | Resistance-repellent retroviral protease inhibitors |
| US7157489B2 (en) * | 2002-03-12 | 2007-01-02 | The Board Of Trustees Of The University Of Illinois | HIV protease inhibitors |
| IL165043A0 (en) | 2002-05-17 | 2005-12-18 | Tibotec Pharm Ltd | broadspectrum substituted benzisoxazole sulfonamide hiv protease inhibitors |
| OA12893A (en) * | 2002-08-02 | 2006-10-13 | Tibotec Pharm Ltd | Broadspectrum 2-Amino-Benzothiazole Sulfonamide HIV Protease Inhibitors. |
| WO2004060895A1 (ja) | 2002-12-27 | 2004-07-22 | Sumitomo Chemical Company, Limited | ヘキサヒドロフロフラノール誘導体の製造方法、その中間体及びその製造方法 |
| JP2007528423A (ja) | 2004-03-11 | 2007-10-11 | セコイア、ファーマシューティカルズ、インコーポレイテッド | 耐性防止レトロウイルスプロテアーゼ阻害薬 |
| TWI383975B (zh) | 2004-03-31 | 2013-02-01 | Tibotec Pharm Ltd | 製備（３Ｒ，３ａＳ，６ａＲ）六氫-呋喃并〔２，３-ｂ〕呋喃-３-醇之方法 |
| KR100698291B1 (ko) * | 2004-12-29 | 2007-03-22 | 엘지전자 주식회사 | 조명계 |
| PT1856125E (pt) | 2005-02-25 | 2009-11-06 | Tibotec Pharm Ltd | Síntese de precursor de inibidor de proteases |
| FR2888849B1 (fr) * | 2005-07-19 | 2007-10-05 | Pierre Fabre Medicament Sa | Procede de preparation de la 4b-amino-4'-demethyl-4-desoxypodophyllotoxine |
| KR101636221B1 (ko) | 2006-07-07 | 2016-07-04 | 길리애드 사이언시즈, 인코포레이티드 | 치료제의 약동학 특성의 모듈레이터 |
| US20080070910A1 (en) * | 2006-07-24 | 2008-03-20 | Desai Manoj C | Therapeutic compounds and methods |
| PL2089371T3 (pl) | 2006-11-09 | 2011-06-30 | Janssen Sciences Ireland Uc | Sposoby wytwarzania heksahydrofuro[2,3-b]furan-3-olu |
| US9808527B2 (en) | 2006-11-21 | 2017-11-07 | Purdue Research Foundation | Methods and compositions for treating HIV infections |
| PL2487162T3 (pl) | 2007-02-23 | 2017-03-31 | Gilead Sciences, Inc. | Modulatory farmakokinetycznych właściwości środków terapeutycznych |
| WO2008115894A1 (en) | 2007-03-16 | 2008-09-25 | Sequoia Pharmaceuticals | Benzofuran-derived hiv protease inhibitors |
| CN101796040A (zh) | 2007-07-06 | 2010-08-04 | 吉里德科学公司 | 治疗剂的药代动力学特性调节剂 |
| ES2555209T3 (es) | 2008-01-04 | 2015-12-29 | Gilead Sciences, Inc. | Inhibidores del citocromo P450 |
| WO2009091941A1 (en) * | 2008-01-17 | 2009-07-23 | Purdue Research Foundation | Small molecule inhibitors of hiv proteases |
| EP2307345A4 (en) * | 2008-07-01 | 2012-05-02 | Purdue Research Foundation | NON-PEPTIDINHIBITORS OF HIV-1 PROTEASE |
| US8501961B2 (en) | 2008-07-09 | 2013-08-06 | Purdue Research Foundation | HIV protease inhibitors and methods for using |
| AU2010338425B2 (en) | 2009-12-21 | 2015-07-23 | Janssen Sciences Ireland Uc | Degradable removable implant for the sustained release of an active compound |
| PL2643326T3 (pl) | 2010-11-23 | 2017-06-30 | Mylan Laboratories, Limited | Sposób przygotowania (3R, 3aS, 6aR)-heksahydrofuro[2,3-b]furan-3-olu |
| WO2014024898A1 (ja) | 2012-08-09 | 2014-02-13 | 住友化学株式会社 | ヘキサヒドロフロフラノール誘導体の製造方法 |
| CN103664976B (zh) * | 2013-12-12 | 2015-11-04 | 惠州市莱佛士制药技术有限公司 | 一种顺式六氢呋喃并[2,3-b]呋喃-3-醇的制备方法 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE154800T1 (de) * | 1992-08-25 | 1997-07-15 | Searle & Co | N-(alkanoylamino-2-hydroxypropyl)-sulfonamide verwendbar als retrovirale proteaseninhibitoren |
| DE69332002T2 (de) * | 1992-08-25 | 2002-12-19 | Monsanto Co | Hydroxyethylaminosulfonamide verwendbar als Inhibitoren retroviraler Proteasen |
| IS2334B (is) * | 1992-09-08 | 2008-02-15 | Vertex Pharmaceuticals Inc., (A Massachusetts Corporation) | Aspartyl próteasi hemjari af nýjum flokki súlfonamíða |
| US5723490A (en) * | 1992-09-08 | 1998-03-03 | Vertex Pharmaceuticals Incorporated | THF-containing sulfonamide inhibitors of aspartyl protease |
| AU7669794A (en) | 1993-08-24 | 1995-03-21 | G.D. Searle & Co. | Hydroxyethylamino sulphonamides useful as retroviral protease inhibitors |
| UA49803C2 (uk) * | 1994-06-03 | 2002-10-15 | Дж.Д. Сьорль Енд Ко | Спосіб лікування ретровірусних інфекцій |
| US5705500A (en) * | 1995-03-10 | 1998-01-06 | G.D. Searle & Co. | Sulfonylalkanoylamino hydroxyethylamino sulfonamide retroviral protease inhibitors |
| US5691372A (en) * | 1995-04-19 | 1997-11-25 | Vertex Pharmaceuticals Incorporated | Oxygenated-Heterocycle containing sulfonamide inhibitors of aspartyl protease |
| EP1088098B2 (en) | 1998-06-23 | 2015-07-01 | THE UNITED STATES OF AMERICA, represented by THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES | Fitness assay and methods for reducing resistance of hiv to therapy |
| WO1999067254A2 (en) * | 1998-06-23 | 1999-12-29 | The United States Of America Represented By The Secretary, Department Of Health And Human Services | Multi-drug resistant retroviral protease inhibitors and use thereof |
| GB9815567D0 (en) * | 1998-07-18 | 1998-09-16 | Glaxo Group Ltd | Antiviral compound |
| CZ300031B6 (cs) * | 1999-10-06 | 2009-01-14 | Tibotec Pharmaceuticals Ltd. | Hexahydrofuro[2,3-b]furan-3-yl-N-{3-[(1,3-benzodioxol-5-ylsulfonyl) (isobutyl)amino]-1-benzyl-2-hydroxypropyl}karbamát a farmaceutický prípravek s jeho obsahem |
-
2000
- 2000-10-06 CZ CZ20021419A patent/CZ300031B6/cs not_active IP Right Cessation
- 2000-10-06 EP EP00966144A patent/EP1222192B8/en not_active Expired - Lifetime
- 2000-10-06 AT AT00966144T patent/ATE398623T1/de not_active IP Right Cessation
- 2000-10-06 AP APAP/P/2002/002472A patent/AP1459A/en active
- 2000-10-06 US US10/089,991 patent/US6649651B1/en not_active Expired - Lifetime
- 2000-10-06 JP JP2001528184A patent/JP4951179B2/ja not_active Expired - Lifetime
- 2000-10-06 KR KR1020027004284A patent/KR100792391B1/ko not_active Expired - Lifetime
- 2000-10-06 IL IL14900500A patent/IL149005A0/xx active IP Right Grant
- 2000-10-06 MX MXPA02003607A patent/MXPA02003607A/es active IP Right Grant
- 2000-10-06 RU RU2002111657/04A patent/RU2247123C2/ru active
- 2000-10-06 PL PL354351A patent/PL204924B1/pl unknown
- 2000-10-06 AU AU76638/00A patent/AU781656B2/en not_active Expired
- 2000-10-06 ES ES00966144T patent/ES2307533T3/es not_active Expired - Lifetime
- 2000-10-06 SK SK570-2002A patent/SK287153B6/sk not_active IP Right Cessation
- 2000-10-06 DE DE60039244T patent/DE60039244D1/de not_active Expired - Lifetime
- 2000-10-06 WO PCT/EP2000/009917 patent/WO2001025240A1/en active IP Right Grant
- 2000-10-06 HU HU0203130A patent/HU228938B1/hu unknown
- 2000-10-06 CA CA2386850A patent/CA2386850C/en not_active Expired - Lifetime
- 2000-10-06 BR BR0014602-1A patent/BR0014602A/pt not_active Application Discontinuation
- 2000-10-06 OA OA1200200096A patent/OA12053A/en unknown
- 2000-10-06 CN CNB008165874A patent/CN1191256C/zh not_active Expired - Lifetime
- 2000-10-06 NZ NZ518580A patent/NZ518580A/en not_active IP Right Cessation
- 2000-10-06 DK DK00966144T patent/DK1222192T3/da active
-
2002
- 2002-04-04 IL IL149005A patent/IL149005A/en unknown
- 2002-04-04 NO NO20021598A patent/NO327996B1/no not_active IP Right Cessation
- 2002-04-04 ZA ZA200202655A patent/ZA200202655B/xx unknown
-
2003
- 2003-06-25 US US10/606,342 patent/US7157495B2/en not_active Expired - Lifetime
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Owner name: THE GOVERNMENT OF THE UNITED STATES OF AMERICA, ES Free format text: FORMER OWNER: JANSSEN R&D IRELAND, EASTGATE, LITTLE ISLAND, CO CORK, IE; THE GOVERNMENT OF T HE UNITED STATES OF AMERICA, REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES; NATIONAL INSTITUTES OF HEALTH OFFICE OF T ECHNOLOGY TRANSFER, ROCKVILLE, MD, US Effective date: 20161206 Owner name: JANSSEN SCIENCES IRELAND UC, EASTGATE, LITTLE , IE Free format text: FORMER OWNER: JANSSEN R&D IRELAND, EASTGATE, LITTLE ISLAND, CO CORK, IE; THE GOVERNMENT OF T HE UNITED STATES OF AMERICA, REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES; NATIONAL INSTITUTES OF HEALTH OFFICE OF T ECHNOLOGY TRANSFER, ROCKVILLE, MD, US Effective date: 20161206 Owner name: NATIONAL INSTITUTES OF HEALTH OFFICE OF TECHNO, US Free format text: FORMER OWNER: JANSSEN R&D IRELAND, EASTGATE, LITTLE ISLAND, CO CORK, IE; THE GOVERNMENT OF T HE UNITED STATES OF AMERICA, REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES; NATIONAL INSTITUTES OF HEALTH OFFICE OF T ECHNOLOGY TRANSFER, ROCKVILLE, MD, US Effective date: 20161206 |
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| TC4A | Change of owner's name |
Owner name: NATIONAL INSTITUTES OF HEALTH OFFICE OF T ECHN, US Effective date: 20161206 Owner name: JANSSEN R&D IRELAND, EASTGATE, LITTLE ISLAND, , IE Effective date: 20161206 Owner name: THE GOVERNMENT OF T HE UNITED STATES OF AMERIC, ES Effective date: 20161206 |
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| MK4A | Expiry of patent |
Expiry date: 20201006 |