AR083268A1 - Conjugado de naloxol-peg cristalino - Google Patents

Conjugado de naloxol-peg cristalino

Info

Publication number
AR083268A1
AR083268A1 ARP110103631A ARP110103631A AR083268A1 AR 083268 A1 AR083268 A1 AR 083268A1 AR P110103631 A ARP110103631 A AR P110103631A AR P110103631 A ARP110103631 A AR P110103631A AR 083268 A1 AR083268 A1 AR 083268A1
Authority
AR
Argentina
Prior art keywords
naloxol
crystal
peg conjugate
salt forms
forms
Prior art date
Application number
ARP110103631A
Other languages
English (en)
Spanish (es)
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=AR083268(A1) "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 AR083268A1 publication Critical patent/AR083268A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C55/00—Saturated compounds having more than one carboxyl group bound to acyclic carbon atoms
    • C07C55/02—Dicarboxylic acids
    • C07C55/06—Oxalic acid
    • C07C55/07—Salts thereof
    • 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
    • A61K47/50—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/56—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 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
    • A61K47/59—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 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
    • A61K47/60—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 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P39/00—General protective or antinoxious agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/41—Preparation of salts of carboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D489/00—Heterocyclic 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:
    • C07D489/02—Heterocyclic 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
    • C07D489/04—Salts; Organic complexes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13—Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Pain & Pain Management (AREA)
  • Toxicology (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)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
ARP110103631A 2010-09-30 2011-09-30 Conjugado de naloxol-peg cristalino AR083268A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US38850110P 2010-09-30 2010-09-30

Publications (1)

Publication Number Publication Date
AR083268A1 true AR083268A1 (es) 2013-02-13

Family

ID=45893441

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP110103631A AR083268A1 (es) 2010-09-30 2011-09-30 Conjugado de naloxol-peg cristalino

Country Status (39)

Country Link
US (2) US9012469B2 (enExample)
EP (2) EP2992903B8 (enExample)
JP (1) JP6034789B2 (enExample)
KR (1) KR101791724B1 (enExample)
CN (1) CN103237547B (enExample)
AR (1) AR083268A1 (enExample)
AU (1) AU2011307608B8 (enExample)
BR (1) BR112013007113B1 (enExample)
CA (1) CA2812649C (enExample)
CL (1) CL2013000866A1 (enExample)
CO (1) CO6700851A2 (enExample)
CR (1) CR20130146A (enExample)
CU (1) CU24317B1 (enExample)
DK (1) DK2621496T4 (enExample)
EA (1) EA023929B1 (enExample)
EC (1) ECSP13012531A (enExample)
ES (2) ES2819305T3 (enExample)
GT (1) GT201300084A (enExample)
HR (1) HRP20151420T4 (enExample)
HU (1) HUE026726T2 (enExample)
IL (1) IL225308A0 (enExample)
ME (1) ME02313B (enExample)
MX (1) MX2013003587A (enExample)
MY (1) MY173890A (enExample)
NI (1) NI201300034A (enExample)
NZ (1) NZ609874A (enExample)
PE (1) PE20140636A1 (enExample)
PH (1) PH12013500561A1 (enExample)
PL (1) PL2621496T5 (enExample)
PT (1) PT2621496E (enExample)
RS (1) RS54488B8 (enExample)
SA (1) SA111320808B1 (enExample)
SG (1) SG188474A1 (enExample)
SI (1) SI2621496T2 (enExample)
SM (1) SMT201600004B (enExample)
TW (1) TWI518088B (enExample)
UA (1) UA112847C2 (enExample)
UY (1) UY33643A (enExample)
WO (1) WO2012044243A1 (enExample)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SI2621496T2 (sl) 2010-09-30 2019-04-30 Astrazeneca Ab Kristalinični konjugat naloksol-PEG
CA2886276A1 (en) * 2012-10-30 2014-05-08 Nektar Therapeutics Solid salt form of alpha-6-mpeg6-o-hydroxycodone as opioid agonists and uses thereof
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 (en) 2016-04-05 2017-10-11 Sandoz Ag Solid dispersion comprising opioid antagonists
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 (en) * 2017-09-19 2019-03-28 Msn Laboratories Private Limited, R&D Center IMPROVED PROCESS FOR THE PREPARATION OF (5Α, 6Α) -17-ALLYL-6- (2,5,8,11,14,17,20-HEPTAOXADOCOSAN-22-YLOXY) -4,5-EPOXYMORPHINANE-3,14-DIOL AND ITS PHARMACEUTICALLY ACCEPTABLE SALTS
JP7690493B2 (ja) * 2020-05-04 2025-06-10 大鵬薬品工業株式会社 Iapアンタゴニスト化合物及びその中間体、並びにそれを合成する方法
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

Family Cites Families (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2507136A (en) † 1949-02-19 1950-05-09 New York Quinine And Chemical Alkaloid purification
EP0668764A1 (en) * 1992-09-21 1995-08-30 QIN, Bo-yi Methods for identifying and using low/non-addictive opioid analgesics
WO1999030727A1 (en) 1997-12-17 1999-06-24 Enzon, Inc. Polymeric prodrugs of amino- and hydroxyl-containing bioactive agents
US6624142B2 (en) 1997-12-30 2003-09-23 Enzon, Inc. Trimethyl lock based tetrapartate prodrugs
EP0995757A3 (en) 1998-08-26 2002-05-22 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Bivalent inhibitors of the proteasome
US6380405B1 (en) 1999-09-13 2002-04-30 Nobex Corporation Taxane prodrugs
CA2394980C (en) 1999-12-22 2008-05-13 Shearwater Corporation Sterically hindered derivatives of water soluble polymers
US6413507B1 (en) 1999-12-23 2002-07-02 Shearwater Corporation Hydrolytically degradable carbamate derivatives of poly (ethylene glycol)
WO2001062299A2 (en) 2000-02-28 2001-08-30 Shearwater Corporation Water-soluble polymer conjugates of artelinic acid
US7829074B2 (en) 2001-10-18 2010-11-09 Nektar Therapeutics Hydroxypatite-targeting poly(ethylene glycol) and related polymers
US20020182172A1 (en) 2000-11-30 2002-12-05 Shearwater Corporation Water-soluble polymer conjugates of triazine derivatives
DE60122580T2 (de) 2000-12-22 2007-08-30 Smithkline Beecham P.L.C., Brentford 5-4'-2'-(n-methyl-n-(2-pyridyl)amino) ethoxy!benzyl!thiazolidin-2,4-dion mesylatsalz
EP1362053B1 (en) 2001-02-20 2007-11-14 Enzon, Inc. Terminally-branched polymeric linkers and polymeric conjugates containing the same
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
US7056500B2 (en) 2001-10-18 2006-06-06 Nektar Therapeutics Al, Corporation Polymer conjugates of opioid antagonists
KR20050040832A (ko) 2001-10-29 2005-05-03 넥타르 테라퓨틱스 에이엘, 코포레이션 단백질 키나아제 c 억제제의 중합체 공액
DE60219677T2 (de) 2001-10-30 2008-05-15 Nektar Therapeutics Al, Corp., Huntsville Wasserlösliche polymerkonjugate von retinoesäure
LT2425821T (lt) * 2002-04-05 2017-07-25 Euro-Celtique S.A. Farmacinis preparatas, turintis oksikodono ir naloksono
GB0317815D0 (en) 2003-07-30 2003-09-03 Amersham Health As Imaging agents
NZ547168A (en) 2003-11-24 2010-05-28 Biogenerix Ag Glycopegylated erythropoietin
US20060182692A1 (en) 2003-12-16 2006-08-17 Fishburn C S Chemically modified small molecules
CN1925875A (zh) 2003-12-16 2007-03-07 尼克塔治疗亚拉巴马公司 化学改性的小分子
US8320574B2 (en) * 2006-04-20 2012-11-27 Hewlett-Packard Development Company, L.P. Methods and systems for reducing acoustic echoes in communication systems
ES2629766T3 (es) 2006-04-21 2017-08-14 Nektar Therapeutics Reducción estereoselectiva de una morfinona
JP2010509227A (ja) * 2006-11-07 2010-03-25 ネクター セラピューティックス エイエル,コーポレイション オピオイド作動薬およびオピオイド拮抗薬の用量形態および同時投与
US8173666B2 (en) 2007-03-12 2012-05-08 Nektar Therapeutics Oligomer-opioid agonist conjugates
CN102014907A (zh) * 2008-05-07 2011-04-13 尼克塔治疗公司 外周作用阿片拮抗剂的口服给药
MX2012000980A (es) † 2009-07-21 2012-06-12 Nektar Therapeutics Conjugados de agonistas de oligómeros-opioides.
SI2621496T2 (sl) 2010-09-30 2019-04-30 Astrazeneca Ab Kristalinični konjugat naloksol-PEG

Also Published As

Publication number Publication date
PH12013500561A1 (en) 2013-06-10
EP2621496B1 (en) 2015-12-16
US9149539B1 (en) 2015-10-06
EP2992903B1 (en) 2020-07-15
SG188474A1 (en) 2013-05-31
MX2013003587A (es) 2013-05-31
KR101791724B9 (ko) 2022-06-16
EP2992903A1 (en) 2016-03-09
ME02313B (me) 2016-06-20
AU2011307608A8 (en) 2015-08-27
TWI518088B (zh) 2016-01-21
BR112013007113A2 (pt) 2017-07-25
AU2011307608A1 (en) 2013-05-02
CU24317B1 (es) 2018-02-08
TW201307356A (zh) 2013-02-16
NI201300034A (es) 2014-01-23
RS54488B1 (sr) 2016-06-30
DK2621496T3 (en) 2016-01-18
BR112013007113B1 (pt) 2020-09-24
ES2562643T5 (es) 2019-05-24
AU2011307608B8 (en) 2015-08-27
CL2013000866A1 (es) 2013-08-30
EA023929B1 (ru) 2016-07-29
US20150038524A1 (en) 2015-02-05
IL225308A0 (en) 2013-06-27
EP2992903B8 (en) 2022-06-08
HRP20151420T1 (hr) 2016-01-29
CR20130146A (es) 2013-05-15
RS54488B8 (sr) 2022-11-30
DK2621496T4 (en) 2019-03-18
JP2013538849A (ja) 2013-10-17
MY173890A (en) 2020-02-26
NZ609874A (en) 2014-10-31
SI2621496T2 (sl) 2019-04-30
HRP20151420T4 (hr) 2019-04-05
US9012469B2 (en) 2015-04-21
RS54488B2 (sr) 2019-03-29
HUE026726T2 (en) 2016-07-28
WO2012044243A1 (en) 2012-04-05
SMT201600004B (it) 2016-02-25
SA111320808B1 (ar) 2014-12-15
PE20140636A1 (es) 2014-06-18
CN103237547A (zh) 2013-08-07
PL2621496T5 (pl) 2019-05-31
PT2621496E (pt) 2016-02-01
GT201300084A (es) 2015-01-16
AU2011307608B2 (en) 2015-04-09
KR20130135844A (ko) 2013-12-11
UA112847C2 (uk) 2016-11-10
ES2562643T3 (es) 2016-03-07
KR101791724B1 (ko) 2017-10-30
HK1187248A1 (zh) 2014-04-04
ECSP13012531A (es) 2013-06-28
CU20130047A7 (es) 2013-08-29
EA201300423A1 (ru) 2013-09-30
EP2621496A1 (en) 2013-08-07
SI2621496T1 (sl) 2016-02-29
PL2621496T3 (pl) 2016-05-31
ES2819305T8 (es) 2022-05-26
ES2562643T8 (es) 2022-07-12
CA2812649C (en) 2016-03-01
CA2812649A1 (en) 2012-04-05
US20150283257A1 (en) 2015-10-08
CN103237547B (zh) 2015-10-07
CO6700851A2 (es) 2013-06-28
ES2819305T3 (es) 2021-04-15
EP2621496B2 (en) 2018-12-12
UY33643A (es) 2012-04-30
JP6034789B2 (ja) 2016-11-30
EP2621496A4 (en) 2014-09-24

Similar Documents

Publication Publication Date Title
CR20130146A (es) Conjugado de naloxol-peg cristalino
ECSP078030A (es) Formas cristalinas y otras formas de las sales de ácido láctico de 4-amino-5-fluoro-3-[6-(4-metilpiperazin -1-il)-1h-bencimidazol-2 -il]-1h-quinolin-2-ona
MX2015004771A (es) Metodos para tratar cancer.
CO6640270A2 (es) Morfolinopirimidad y su uso en terapia
CL2011000589A1 (es) Compuestos derivados de pirrolidin-2-carboxamida, inhibidores de la interaccion p53-mdm2; composicion farmaceutica que los comprende; y su uso en la preparacion de medicamentos utiles para el tratamiento del cancer.
BR112014009087A2 (pt) formulações de etanercept estabilizadas com xilitol
ECSP12012208A (es) Formulaciones orales y sales lipofílicas de metilnaltrexona
ECSP099721A (es) Inhibidores de cinasa p70 s6
UY32649A (es) "sales de 4-(dimetilamino)butil 2-(4-((2-amino-4-metil-6-(pentilamino)pirimidin-5-il)metil)fenil)acetato"
BR112015000229A2 (pt) formulações aquosas estáveis de etanercept
GT200800285A (es) Aminopirazolopiridinas sustituidas y sus sales, sus preparaciones y composiciones farmaceuticas que las comprenden
CR20110216A (es) Derivados de ácido 1-amino-2-ciclobutiletilborónico
CR11333A (es) cis-IMIDAZOLINAS QUIRALES
MX2015012414A (es) Sal de omecamtiv mecarbilo y proceso para preparar la sal.
ECSP14013215A (es) Compuestos novedosos
ECSP088288A (es) DERIVADOS DE 7-(2-AMINO-1-HIDROXI-ETIL)-4-HIDROXIBENZOTIAZOL-2(3H)-ONA COMO AGONISTAS DE LOS ADRENOCEPTORES ß2
CO7091174A2 (es) Compuestos triazolo como inhibidores de pde10
CO6640301A2 (es) Compuestos ologo-benzamida y su uso
SV2010003752A (es) Derivados de urea heterociclicos para el tratamiento de infecciones bacterianas
BR112013030605A2 (pt) formulações orais de antioxidantes direcionados mitocondrialmente e preparação e uso dos mesmos
AR063027A1 (es) Derivados de sulfonamida
BR112014026817A2 (pt) derivados do pantotenato para o tratamento de transtornos neurológicos
BR112016010051A2 (pt) ?conjugados de anticorpo-fármaco anti-efna4?
UY34552A (es) Forma cristalina delta de la sal de arginina de perindoprilo, su procedimiento de preparación, y las composiciones farmacéuticas que la contienen
MX2015005510A (es) Forma salina solida de la alfa-6-mpeg6-o-hidroxicodona como agonistas opioides y sus usos.

Legal Events

Date Code Title Description
FC Refusal