NO332842B1 - NTP-peptider, deres anvendelse og sammensetning omfattende det samme - Google Patents
NTP-peptider, deres anvendelse og sammensetning omfattende det samme Download PDFInfo
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- NO332842B1 NO332842B1 NO20041844A NO20041844A NO332842B1 NO 332842 B1 NO332842 B1 NO 332842B1 NO 20041844 A NO20041844 A NO 20041844A NO 20041844 A NO20041844 A NO 20041844A NO 332842 B1 NO332842 B1 NO 332842B1
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Classifications
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- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
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- 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
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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Landscapes
- Health & Medical Sciences (AREA)
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US33147701P | 2001-11-16 | 2001-11-16 | |
PCT/CA2002/001757 WO2003044053A2 (en) | 2001-11-16 | 2002-11-18 | Peptides effective in the treatment of tumors and other conditions requiring the removal or destruction of cells |
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NO20041844L NO20041844L (no) | 2004-07-06 |
NO332842B1 true NO332842B1 (no) | 2013-01-21 |
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NO20041844A NO332842B1 (no) | 2001-11-16 | 2004-05-04 | NTP-peptider, deres anvendelse og sammensetning omfattende det samme |
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EP (1) | EP1442058B1 (pt) |
JP (2) | JP4717349B2 (pt) |
KR (4) | KR20120123573A (pt) |
CN (1) | CN100509846C (pt) |
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AU (1) | AU2002342463B2 (pt) |
BR (1) | BRPI0213786B8 (pt) |
CA (1) | CA2467053C (pt) |
CY (1) | CY1107578T1 (pt) |
DE (1) | DE60213274T2 (pt) |
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NO (1) | NO332842B1 (pt) |
NZ (1) | NZ532721A (pt) |
PL (1) | PL207591B1 (pt) |
PT (1) | PT1442058E (pt) |
WO (1) | WO2003044053A2 (pt) |
ZA (1) | ZA200403624B (pt) |
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US7317077B2 (en) * | 2001-11-16 | 2008-01-08 | Nymox Pharmaceutical Corporation | Peptides effective in the treatment of tumors and other conditions requiring the removal or destruction of cells |
CN1867299B (zh) | 2003-09-12 | 2010-09-29 | 明诺医学有限公司 | 动脉粥样硬化物的可选择偏心重塑和/或消融 |
US20090232866A1 (en) * | 2003-10-07 | 2009-09-17 | Mariann Pavone-Gyongyosi | Oligopeptides as coating material for medical products |
CN1965082A (zh) * | 2004-02-06 | 2007-05-16 | 尼莫克斯股份有限公司 | 人源化抗体 |
US8396548B2 (en) | 2008-11-14 | 2013-03-12 | Vessix Vascular, Inc. | Selective drug delivery in a lumen |
US9713730B2 (en) | 2004-09-10 | 2017-07-25 | Boston Scientific Scimed, Inc. | Apparatus and method for treatment of in-stent restenosis |
CN100427502C (zh) * | 2005-06-09 | 2008-10-22 | 南京大学 | 抗肿瘤寡肽及其制备方法和应用 |
DK1994152T3 (da) * | 2006-02-28 | 2013-03-11 | Nymox Corp | Peptider der er effektive i behandlingen af tumorer og andre tilstande der kræver fjernelse eller destruktion af celler |
WO2007104149A1 (en) * | 2006-03-10 | 2007-09-20 | Nymox Corporation | Method of preventing or reducing the risk or incidence of cancer using neural thread protein based peptides |
US8019435B2 (en) | 2006-05-02 | 2011-09-13 | Boston Scientific Scimed, Inc. | Control of arterial smooth muscle tone |
US20080027005A1 (en) * | 2006-07-31 | 2008-01-31 | Paul Averback | Peptides effective in the treatment of tumors and other conditions requiring the removal or destruction of cells |
AU2007310991B2 (en) | 2006-10-18 | 2013-06-20 | Boston Scientific Scimed, Inc. | System for inducing desirable temperature effects on body tissue |
EP2076193A4 (en) | 2006-10-18 | 2010-02-03 | Minnow Medical Inc | MATCHED RF-ENERGY AND ELECTRO-TISSUE CHARACTERIZATION FOR THE SELECTIVE TREATMENT OF TARGET TISSUE |
EP2992850A1 (en) | 2006-10-18 | 2016-03-09 | Vessix Vascular, Inc. | Inducing desirable temperature effects on body tissue |
KR20110104504A (ko) | 2008-11-17 | 2011-09-22 | 미노우 메디컬, 인코포레이티드 | 조직 토폴로지의 지식 여하에 따른 에너지의 선택적 축적 |
JP5625043B2 (ja) * | 2009-04-13 | 2014-11-12 | ザ・フェインスタイン・インスティチュート・フォー・メディカル・リサーチThe Feinstein Institute for Medical Research | 低温誘導性rna結合タンパク質(cirp)を阻害することによる炎症性疾患の治療 |
KR20130108067A (ko) | 2010-04-09 | 2013-10-02 | 베식스 바스큘라 인코포레이티드 | 조직 치료를 위한 발전 및 제어 장치 |
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US10549127B2 (en) | 2012-09-21 | 2020-02-04 | Boston Scientific Scimed, Inc. | Self-cooling ultrasound ablation catheter |
US10835305B2 (en) | 2012-10-10 | 2020-11-17 | Boston Scientific Scimed, Inc. | Renal nerve modulation devices and methods |
WO2014143571A1 (en) | 2013-03-11 | 2014-09-18 | Boston Scientific Scimed, Inc. | Medical devices for modulating nerves |
WO2014163987A1 (en) | 2013-03-11 | 2014-10-09 | Boston Scientific Scimed, Inc. | Medical devices for modulating nerves |
US9808311B2 (en) | 2013-03-13 | 2017-11-07 | Boston Scientific Scimed, Inc. | Deflectable medical devices |
US10265122B2 (en) | 2013-03-15 | 2019-04-23 | Boston Scientific Scimed, Inc. | Nerve ablation devices and related methods of use |
EP2967734B1 (en) | 2013-03-15 | 2019-05-15 | Boston Scientific Scimed, Inc. | Methods and apparatuses for remodeling tissue of or adjacent to a body passage |
AU2014237950B2 (en) | 2013-03-15 | 2017-04-13 | Boston Scientific Scimed, Inc. | Control unit for use with electrode pads and a method for estimating an electrical leakage |
US9943365B2 (en) | 2013-06-21 | 2018-04-17 | Boston Scientific Scimed, Inc. | Renal denervation balloon catheter with ride along electrode support |
WO2014205399A1 (en) | 2013-06-21 | 2014-12-24 | Boston Scientific Scimed, Inc. | Medical devices for renal nerve ablation having rotatable shafts |
US9707036B2 (en) | 2013-06-25 | 2017-07-18 | Boston Scientific Scimed, Inc. | Devices and methods for nerve modulation using localized indifferent electrodes |
CN105358084B (zh) | 2013-07-01 | 2018-11-09 | 波士顿科学国际有限公司 | 用于肾神经消融的医疗器械 |
EP3019105B1 (en) | 2013-07-11 | 2017-09-13 | Boston Scientific Scimed, Inc. | Devices for nerve modulation |
US10413357B2 (en) | 2013-07-11 | 2019-09-17 | Boston Scientific Scimed, Inc. | Medical device with stretchable electrode assemblies |
EP3049007B1 (en) | 2013-07-19 | 2019-06-12 | Boston Scientific Scimed, Inc. | Spiral bipolar electrode renal denervation balloon |
CN105555220B (zh) | 2013-07-22 | 2019-05-17 | 波士顿科学国际有限公司 | 用于肾神经消融的医疗器械 |
EP3024405A1 (en) | 2013-07-22 | 2016-06-01 | Boston Scientific Scimed, Inc. | Renal nerve ablation catheter having twist balloon |
JP6159888B2 (ja) | 2013-08-22 | 2017-07-05 | ボストン サイエンティフィック サイムド,インコーポレイテッドBoston Scientific Scimed,Inc. | 腎神経変調バルーンへの接着性を向上させたフレキシブル回路 |
US9895194B2 (en) | 2013-09-04 | 2018-02-20 | Boston Scientific Scimed, Inc. | Radio frequency (RF) balloon catheter having flushing and cooling capability |
WO2015038947A1 (en) | 2013-09-13 | 2015-03-19 | Boston Scientific Scimed, Inc. | Ablation balloon with vapor deposited cover layer |
CN105764923A (zh) | 2013-09-24 | 2016-07-13 | 范因斯坦医学研究院 | 对可冷诱导的rna结合蛋白活性进行抑制的肽 |
US11246654B2 (en) | 2013-10-14 | 2022-02-15 | Boston Scientific Scimed, Inc. | Flexible renal nerve ablation devices and related methods of use and manufacture |
EP3057488B1 (en) | 2013-10-14 | 2018-05-16 | Boston Scientific Scimed, Inc. | High resolution cardiac mapping electrode array catheter |
US9770606B2 (en) | 2013-10-15 | 2017-09-26 | Boston Scientific Scimed, Inc. | Ultrasound ablation catheter with cooling infusion and centering basket |
EP3057520A1 (en) | 2013-10-15 | 2016-08-24 | Boston Scientific Scimed, Inc. | Medical device balloon |
WO2015057961A1 (en) | 2013-10-18 | 2015-04-23 | Boston Scientific Scimed, Inc. | Balloon catheters with flexible conducting wires and related methods of use and manufacture |
EP3060153A1 (en) | 2013-10-25 | 2016-08-31 | Boston Scientific Scimed, Inc. | Embedded thermocouple in denervation flex circuit |
WO2015103617A1 (en) | 2014-01-06 | 2015-07-09 | Boston Scientific Scimed, Inc. | Tear resistant flex circuit assembly |
JP6325121B2 (ja) | 2014-02-04 | 2018-05-16 | ボストン サイエンティフィック サイムド,インコーポレイテッドBoston Scientific Scimed,Inc. | 双極電極上の温度センサの代替配置 |
US11000679B2 (en) | 2014-02-04 | 2021-05-11 | Boston Scientific Scimed, Inc. | Balloon protection and rewrapping devices and related methods of use |
US20160215031A1 (en) * | 2015-01-27 | 2016-07-28 | Nymox Pharnaceutical Corporation | Method of treating disorders requiring destruction or removal of cells |
US10078207B2 (en) | 2015-03-18 | 2018-09-18 | Endochoice, Inc. | Systems and methods for image magnification using relative movement between an image sensor and a lens assembly |
US20160361380A1 (en) | 2015-06-12 | 2016-12-15 | Nymox Corporation | Combination compositions for treating disorders requiring removal or destruction of unwanted cellular proliferations |
US10583167B2 (en) * | 2015-06-29 | 2020-03-10 | The University Of British Columbia | Mammalian glucosidase inhibitors, methods for their use and pharmaceutical compositions thereof |
US11628202B2 (en) * | 2015-07-24 | 2023-04-18 | Nymox Corporation | Methods of reducing the need for surgery in patients suffering from benign prostatic hyperplasia |
US10183058B2 (en) * | 2016-06-17 | 2019-01-22 | Nymox Corporation | Method of preventing or reducing the progression of prostate cancer |
US10172910B2 (en) | 2016-07-28 | 2019-01-08 | Nymox Corporation | Method of preventing or reducing the incidence of acute urinary retention |
US10532081B2 (en) | 2016-09-07 | 2020-01-14 | Nymox Corporation | Method of ameliorating or preventing the worsening or the progression of symptoms of BPH |
US10335453B2 (en) | 2017-03-01 | 2019-07-02 | Nymox Corporation | Compositions and methods for improving sexual function |
US10835538B2 (en) | 2018-03-28 | 2020-11-17 | Nymox Corporation | Method of treating benign prostatic hyperlasia with antibiotics |
US20200061150A1 (en) * | 2018-08-23 | 2020-02-27 | Nymox Corporation | Method of inducing selective prostate glandular pharmaco-ablation with sparing of nerves and preservation of sexual function |
US20200360466A1 (en) | 2019-05-13 | 2020-11-19 | Nymox Corporation | Method of improving lower urinary tract symptoms |
US11298400B2 (en) | 2019-05-13 | 2022-04-12 | Nymox Corporation | Method of enhancing the therapeutic efficacy of fexapotide triflutate in treating LUTS |
US11278588B2 (en) | 2019-05-13 | 2022-03-22 | Nymox Corporation | Method of treating lower urinary tract symptoms with fexapotide triflutate |
US11231421B2 (en) | 2019-07-31 | 2022-01-25 | Nymox Corporation | Methods of treating multifocal cancer |
US11331374B2 (en) | 2019-07-31 | 2022-05-17 | Nymox Corporation | Focal treatment of prostate cancer |
Family Cites Families (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US594863A (en) * | 1897-12-07 | Otto p | ||
US5169933A (en) * | 1988-08-15 | 1992-12-08 | Neorx Corporation | Covalently-linked complexes and methods for enhanced cytotoxicity and imaging |
US5948634A (en) * | 1988-12-21 | 1999-09-07 | The General Hospital Coporation | Neural thread protein gene expression and detection of alzheimer's disease |
JP3309972B2 (ja) * | 1988-12-21 | 2002-07-29 | ザ・ジェネラル・ホスピタル・コーポレイション | 神経系疾患または機能障害の検出法 |
JPH06256387A (ja) | 1991-06-14 | 1994-09-13 | Suetsuna Yoko | 新規なペプチド、その製法およびそれを有効成分とする 血圧降下剤 |
DK0697893T3 (da) | 1993-04-20 | 2006-02-20 | Gen Hospital Corp | Nervetrådproteingenekspression og detektion af Alzheimers sygdom |
FR2757486B1 (fr) | 1996-12-24 | 1999-03-26 | Sanofi Sa | Receptacle de conditionnement de deux produits pouvant s'ecouler et maintenus separes avant d'etre melanges pour utilisation |
EP0975651A4 (en) | 1997-02-26 | 2005-03-09 | Gen Hospital Corp | TRANSGENIC ANIMALS AND CELL LINES FOR THE SCREENING OF MEDICAMENTS FOR THE TREATMENT OR PREVENTION OF ALZHEIMER'S DISEASE |
US6238667B1 (en) * | 1997-09-19 | 2001-05-29 | Heinz Kohler | Method of affinity cross-linking biologically active immunogenic peptides to antibodies |
CA2335986A1 (en) * | 1998-06-26 | 2000-01-06 | Simeng Suy | Use of tempo and tempo derivatives for inducing cell death |
AU2185199A (en) * | 1998-09-30 | 2000-04-17 | Yoko Aida | Apoptosis inducers |
AU2373800A (en) * | 1998-12-11 | 2000-06-26 | Incyte Pharmaceuticals, Inc. | Neuron-associated proteins |
EA200100770A1 (ru) * | 1999-01-11 | 2002-02-28 | Леадд Б.В. | Применение агентов, индуцирующих апоптоз, в лечении (ауто)имунных заболеваний |
WO2000055198A1 (en) | 1999-03-12 | 2000-09-21 | Human Genome Sciences, Inc. | 50 human secreted proteins |
WO2000063230A2 (en) | 1999-03-26 | 2000-10-26 | Human Genome Sciences, Inc. | 49 human secreted proteins |
WO2000056767A1 (en) | 1999-03-19 | 2000-09-28 | Human Genome Sciences, Inc. | 46 human secreted proteins |
EP1220947A2 (en) | 1999-03-26 | 2002-07-10 | Human Genome Sciences, Inc. | 50 human secreted proteins |
EP1165827A4 (en) | 1999-03-26 | 2003-05-02 | Human Genome Sciences Inc | 45 HUMAN SECRETED PROTEINS |
WO2001035921A1 (en) | 1999-11-16 | 2001-05-25 | Unilever Plc | Cosmetic compositions containing anise extract and retinoids |
AU1940001A (en) | 1999-11-30 | 2001-06-12 | Curagen Corporation | Nucleic acids containing single nucleotide polymorphisms and methods of use thereof |
CN1300779A (zh) | 1999-12-22 | 2001-06-27 | 上海博德基因开发有限公司 | 一种新的多肽-人神经元线蛋白17和编码这种多肽的多核苷酸 |
CN1300783A (zh) | 1999-12-23 | 2001-06-27 | 上海生元基因开发有限公司 | 新的人神经元线蛋白及其编码序列 |
WO2002000718A2 (en) | 2000-06-26 | 2002-01-03 | Millennium Pharmaceuticals, Inc. | A human calcium channel protein and uses thereof |
US6783969B1 (en) | 2001-03-05 | 2004-08-31 | Nuvelo, Inc. | Cathepsin V-like polypeptides |
EP1392347B1 (en) * | 2001-05-16 | 2005-08-03 | Nymox Corporation | Preventing cell death using segments of neural thread proteins |
CA2448348C (en) * | 2001-05-25 | 2013-07-16 | Nymox Corporation | Peptides effective in the treatment of tumors and other conditions requiring the removal or destruction of cells |
KR101005130B1 (ko) * | 2001-07-19 | 2011-01-04 | 니목스 코포레이션 | 종양 및 세포의 제거 또는 파괴를 필요로 하는 다른질환의 치료에 효과적인 펩티드 |
US7317077B2 (en) * | 2001-11-16 | 2008-01-08 | Nymox Pharmaceutical Corporation | Peptides effective in the treatment of tumors and other conditions requiring the removal or destruction of cells |
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