CU24317B1 - Conjugado de naloxol-peg cristalino - Google Patents

Conjugado de naloxol-peg cristalino

Info

Publication number
CU24317B1
CU24317B1 CUP2013000047A CU20130047A CU24317B1 CU 24317 B1 CU24317 B1 CU 24317B1 CU P2013000047 A CUP2013000047 A CU P2013000047A CU 20130047 A CU20130047 A CU 20130047A CU 24317 B1 CU24317 B1 CU 24317B1
Authority
CU
Cuba
Prior art keywords
naloxol
crystal
peg conjugate
salt forms
formula
Prior art date
Application number
CUP2013000047A
Other languages
English (en)
Spanish (es)
Other versions
CU20130047A7 (es
Inventor
Bengt Leonard Aslund
Carl Johan Aurell
Martin Hans Bohlin
Eric Thomas Healy
David Richard Jensen
David Thomas Jonaitis
Stephan Parent
Tesfai Sebhatu
Bo Ingvar Ymen
Original Assignee
Astrazeneca Ab
Nektar Therapeutics
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=45893441&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CU24317(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Astrazeneca Ab, Nektar Therapeutics filed Critical Astrazeneca Ab
Publication of CU20130047A7 publication Critical patent/CU20130047A7/es
Publication of CU24317B1 publication Critical patent/CU24317B1/xx

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C55/00Saturated compounds having more than one carboxyl group bound to acyclic carbon atoms
    • C07C55/02Dicarboxylic acids
    • C07C55/06Oxalic acid
    • C07C55/07Salts thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/56Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule
    • A61K47/59Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas or polyurethanes
    • A61K47/60Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas or polyurethanes the organic macromolecular compound being a polyoxyalkylene oligomer, polymer or dendrimer, e.g. PEG, PPG, PEO or polyglycerol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P39/00General protective or antinoxious agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/41Preparation of salts of carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D489/00Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula:
    • C07D489/02Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula: with oxygen atoms attached in positions 3 and 6, e.g. morphine, morphinone
    • C07D489/04Salts; Organic complexes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Toxicology (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Emergency Medicine (AREA)
  • Compression Or Coding Systems Of Tv Signals (AREA)
CUP2013000047A 2010-09-30 2011-09-29 Conjugado de naloxol-peg cristalino CU24317B1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US38850110P 2010-09-30 2010-09-30
PCT/SE2011/051161 WO2012044243A1 (fr) 2010-09-30 2011-09-29 Conjugué cristallin de naloxol-peg

Publications (2)

Publication Number Publication Date
CU20130047A7 CU20130047A7 (es) 2013-08-29
CU24317B1 true CU24317B1 (es) 2018-02-08

Family

ID=45893441

Family Applications (1)

Application Number Title Priority Date Filing Date
CUP2013000047A CU24317B1 (es) 2010-09-30 2011-09-29 Conjugado de naloxol-peg cristalino

Country Status (39)

Country Link
US (2) US9012469B2 (fr)
EP (2) EP2992903B8 (fr)
JP (1) JP6034789B2 (fr)
KR (1) KR101791724B1 (fr)
CN (1) CN103237547B (fr)
AR (1) AR083268A1 (fr)
AU (1) AU2011307608B8 (fr)
BR (1) BR112013007113B1 (fr)
CA (1) CA2812649C (fr)
CL (1) CL2013000866A1 (fr)
CO (1) CO6700851A2 (fr)
CR (1) CR20130146A (fr)
CU (1) CU24317B1 (fr)
DK (1) DK2621496T4 (fr)
EA (1) EA023929B1 (fr)
EC (1) ECSP13012531A (fr)
ES (2) ES2562643T5 (fr)
GT (1) GT201300084A (fr)
HK (1) HK1187248A1 (fr)
HR (1) HRP20151420T4 (fr)
HU (1) HUE026726T2 (fr)
IL (1) IL225308A0 (fr)
ME (1) ME02313B (fr)
MX (1) MX2013003587A (fr)
MY (1) MY173890A (fr)
NI (1) NI201300034A (fr)
NZ (1) NZ609874A (fr)
PE (1) PE20140636A1 (fr)
PL (1) PL2621496T5 (fr)
PT (1) PT2621496E (fr)
RS (1) RS54488B8 (fr)
SA (1) SA111320808B1 (fr)
SG (1) SG188474A1 (fr)
SI (1) SI2621496T2 (fr)
SM (1) SMT201600004B (fr)
TW (1) TWI518088B (fr)
UA (1) UA112847C2 (fr)
UY (1) UY33643A (fr)
WO (1) WO2012044243A1 (fr)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9012469B2 (en) 2010-09-30 2015-04-21 Astrazeneca Ab Crystalline naloxol-peg conjugate
PL2914599T3 (pl) * 2012-10-30 2018-05-30 Nektar Therapeutics Stałe postacie soli alfa-6-MPEG6-O-hydroksykodonu jako agoniści opioidowi i ich zastosowania
CN107660207B (zh) * 2015-03-10 2020-09-29 罗德科技公司 丁丙诺啡乙酸盐及用于制备丁丙诺啡的方法
CN107033154B (zh) * 2016-02-02 2020-02-04 上海瀚迈生物医药科技有限公司 阿片受体拮抗剂缀合物及其应用
CN107033155B (zh) * 2016-02-04 2019-04-26 国药集团国瑞药业有限公司 一种吗啡酮类化合物的立体选择性还原方法
EP3228307A1 (fr) 2016-04-05 2017-10-11 Sandoz Ag Solid dispersion contenant des antagonistes opioides
CN107303392A (zh) * 2016-04-19 2017-10-31 石家庄蒎格医药科技有限公司 一种聚乙二醇-纳洛酮组合物及应用
US11077103B2 (en) * 2016-11-23 2021-08-03 Aurobindo Pharma Ltd. Naloxegol oxalate and solid dispersion thereof
US11373198B2 (en) * 2016-12-02 2022-06-28 Honda Motor Co., Ltd. Evaluation device, evaluation method, and evaluation program
WO2019058387A1 (fr) * 2017-09-19 2019-03-28 Msn Laboratories Private Limited, R&D Center Procédé amélioré de préparation de (5α,6α)-17-allyl-6-(2,5,8,11,14,17,20-heptaoxadocosan-22-yloxy) -4,5-époxymorphinane-3,14-diol et de ses sels pharmaceutiquement acceptables
CN114137133B (zh) * 2021-12-03 2023-06-09 北京尚修堂医药科技有限公司 一种纳洛醇-peg衍生物有关物质的检测方法

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US2507136A (en) 1949-02-19 1950-05-09 New York Quinine And Chemical Alkaloid purification
EP0668764A1 (fr) * 1992-09-21 1995-08-30 QIN, Bo-yi Procedes d'identification et d'utilisation d'analgesiques opioides de faible dependance ou de non dependance
EP1037649B1 (fr) 1997-12-17 2009-09-30 Enzon, Inc. Prodrogues polymeriques d'agents bioactifs contenant amine ou hydroxy
US6624142B2 (en) 1997-12-30 2003-09-23 Enzon, Inc. Trimethyl lock based tetrapartate prodrugs
EP0995757A3 (fr) 1998-08-26 2002-05-22 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Inhibiteurs bivalentes de la proteasome
US6380405B1 (en) 1999-09-13 2002-04-30 Nobex Corporation Taxane prodrugs
JP4861586B2 (ja) 1999-12-22 2012-01-25 ネクター セラピューティックス 水溶性ポリマーの立体的に妨害される誘導体
US6413507B1 (en) 1999-12-23 2002-07-02 Shearwater Corporation Hydrolytically degradable carbamate derivatives of poly (ethylene glycol)
WO2001062299A2 (fr) 2000-02-28 2001-08-30 Shearwater Corporation Conjugues polymeres hydrosolubles d'acide artelinique
US7829074B2 (en) 2001-10-18 2010-11-09 Nektar Therapeutics Hydroxypatite-targeting poly(ethylene glycol) and related polymers
JP2004514701A (ja) 2000-11-30 2004-05-20 ネクター セラピューティクス エーエル,コーポレイション トリアジン誘導体の水溶性ポリマー複合体
PT1349855E (pt) 2000-12-22 2006-12-29 Smithkline Beecham Plc Sal misilato de 5-{4-[2-(n-metil-n-(2-piridil)amino)etoxi]benzil}tiazolidino-2, 4-diona
CA2437989A1 (fr) 2001-02-20 2002-08-29 Enzon, Inc. Lieurs polymeres a terminaisons ramifiees, et conjugues polymeres en contenant
US6828305B2 (en) 2001-06-04 2004-12-07 Nobex Corporation Mixtures of growth hormone drug-oligomer conjugates comprising polyalkylene glycol, uses thereof, and methods of making same
US6713452B2 (en) 2001-06-04 2004-03-30 Nobex Corporation Mixtures of calcitonin drug-oligomer conjugates comprising polyalkylene glycol, uses thereof, and methods of making same
US6756354B2 (en) 2001-09-05 2004-06-29 Deanna Jean Nelson Therapeutic compositions containing oligo (ethylene glycol)-terminated 1,2-dithiolanes and their conjugates
CA2463938C (fr) 2001-10-18 2011-08-09 Nektar Therapeutics Al, Corporation Conjugues polymeres d'antagonistes opioides
EP1441772A2 (fr) 2001-10-29 2004-08-04 Nektar Therapeutics Al, Corporation Conjugues polymeres d'inhibiteurs de proteine kinease c
ATE359829T1 (de) 2001-10-30 2007-05-15 Nektar Therapeutics Al Corp Wasserlösliche polymerkonjugate von retinoesäure
ES2733044T1 (es) 2002-04-05 2019-11-27 Mundipharma Pharmaceuticals S L Composición farmacéutica que contiene oxicodona y naloxona
GB0317815D0 (en) 2003-07-30 2003-09-03 Amersham Health As Imaging agents
CA2547140A1 (fr) 2003-11-24 2005-06-09 Neose Technologies, Inc. Erythropoietine glycopegylee
CA2758460C (fr) 2003-12-16 2014-09-23 Nektar Therapeutics Methodes de preparation de compositions de reactifs oligo (ethylene glycol) monodisperses
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NZ572252A (en) 2006-04-21 2011-09-30 Nektar Therapeutics Stereoselective reduction of a morphinone
MX2009004965A (es) * 2006-11-07 2009-06-05 Nektar Therapeutics Al Corp Formas de dosificacion y co-administracion de un agonista de opioides y un antagonista de opioides.
US8173666B2 (en) 2007-03-12 2012-05-08 Nektar Therapeutics Oligomer-opioid agonist conjugates
BRPI0912219A2 (pt) 2008-05-07 2015-10-06 Nektar Therapeutics método, forma de dose unitária, e, antagonista de opióide oralmente administrável que atua perifericamente.
CA2768392C (fr) 2009-07-21 2018-04-17 Nektar Therapeutics Conjugues oligomeres-agonistes opioides
US9012469B2 (en) 2010-09-30 2015-04-21 Astrazeneca Ab Crystalline naloxol-peg conjugate

Also Published As

Publication number Publication date
GT201300084A (es) 2015-01-16
JP6034789B2 (ja) 2016-11-30
EP2992903A1 (fr) 2016-03-09
TW201307356A (zh) 2013-02-16
EP2621496A1 (fr) 2013-08-07
SG188474A1 (en) 2013-05-31
AU2011307608B2 (en) 2015-04-09
EP2621496B1 (fr) 2015-12-16
NZ609874A (en) 2014-10-31
RS54488B8 (sr) 2022-11-30
NI201300034A (es) 2014-01-23
DK2621496T4 (en) 2019-03-18
ECSP13012531A (es) 2013-06-28
ES2819305T3 (es) 2021-04-15
UA112847C2 (uk) 2016-11-10
HK1187248A1 (zh) 2014-04-04
ME02313B (me) 2016-06-20
SI2621496T1 (sl) 2016-02-29
HRP20151420T4 (hr) 2019-04-05
JP2013538849A (ja) 2013-10-17
UY33643A (es) 2012-04-30
AU2011307608A1 (en) 2013-05-02
CN103237547A (zh) 2013-08-07
CN103237547B (zh) 2015-10-07
KR101791724B9 (ko) 2022-06-16
CR20130146A (es) 2013-05-15
BR112013007113A2 (pt) 2017-07-25
EP2992903B1 (fr) 2020-07-15
ES2562643T8 (es) 2022-07-12
CO6700851A2 (es) 2013-06-28
KR20130135844A (ko) 2013-12-11
AU2011307608B8 (en) 2015-08-27
US9012469B2 (en) 2015-04-21
DK2621496T3 (en) 2016-01-18
AR083268A1 (es) 2013-02-13
HUE026726T2 (en) 2016-07-28
BR112013007113B1 (pt) 2020-09-24
US20150283257A1 (en) 2015-10-08
AU2011307608A8 (en) 2015-08-27
CA2812649A1 (fr) 2012-04-05
IL225308A0 (en) 2013-06-27
CU20130047A7 (es) 2013-08-29
EA201300423A1 (ru) 2013-09-30
EP2992903B8 (fr) 2022-06-08
HRP20151420T1 (hr) 2016-01-29
ES2819305T8 (es) 2022-05-26
MY173890A (en) 2020-02-26
MX2013003587A (es) 2013-05-31
EP2621496B2 (fr) 2018-12-12
SMT201600004B (it) 2016-02-25
ES2562643T5 (es) 2019-05-24
RS54488B1 (en) 2016-06-30
SA111320808B1 (ar) 2014-12-15
CA2812649C (fr) 2016-03-01
RS54488B2 (sr) 2019-03-29
PL2621496T3 (pl) 2016-05-31
CL2013000866A1 (es) 2013-08-30
PT2621496E (pt) 2016-02-01
ES2562643T3 (es) 2016-03-07
PE20140636A1 (es) 2014-06-18
US9149539B1 (en) 2015-10-06
EP2621496A4 (fr) 2014-09-24
TWI518088B (zh) 2016-01-21
US20150038524A1 (en) 2015-02-05
PL2621496T5 (pl) 2019-05-31
EA023929B1 (ru) 2016-07-29
WO2012044243A1 (fr) 2012-04-05
KR101791724B1 (ko) 2017-10-30
SI2621496T2 (sl) 2019-04-30

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