CA2812649C - Crystalline naloxol-peg conjugate - Google Patents

Crystalline naloxol-peg conjugate Download PDF

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Publication number
CA2812649C
CA2812649C CA2812649A CA2812649A CA2812649C CA 2812649 C CA2812649 C CA 2812649C CA 2812649 A CA2812649 A CA 2812649A CA 2812649 A CA2812649 A CA 2812649A CA 2812649 C CA2812649 C CA 2812649C
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CA
Canada
Prior art keywords
naloxol
mpeg7
salt
oxalate salt
polyethylene glycol
Prior art date
Legal status (The legal status 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 status listed.)
Active
Application number
CA2812649A
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English (en)
French (fr)
Other versions
CA2812649A1 (en
Inventor
Bengt Leonard Aslund
Carl-Johan Aurell
Martin Hans Bohlin
Tesfai Sebhatu
Bo Ingvar Ymen
Eric Thomas Healy
David Richard Jensen
David Thomas Jonaitis
Stephan Parent
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
AstraZeneca AB
Nektar Therapeutics
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AstraZeneca AB
Nektar Therapeutics
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Application filed by AstraZeneca AB, Nektar Therapeutics filed Critical AstraZeneca AB
Publication of CA2812649A1 publication Critical patent/CA2812649A1/en
Application granted granted Critical
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    • 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

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (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)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Compression Or Coding Systems Of Tv Signals (AREA)
CA2812649A 2010-09-30 2011-09-29 Crystalline naloxol-peg conjugate Active CA2812649C (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US38850110P 2010-09-30 2010-09-30
US61/388,501 2010-09-30
PCT/SE2011/051161 WO2012044243A1 (en) 2010-09-30 2011-09-29 Crystalline naloxol-peg conjugate

Publications (2)

Publication Number Publication Date
CA2812649A1 CA2812649A1 (en) 2012-04-05
CA2812649C true CA2812649C (en) 2016-03-01

Family

ID=45893441

Family Applications (1)

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CA2812649A Active CA2812649C (en) 2010-09-30 2011-09-29 Crystalline naloxol-peg conjugate

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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) ES2562643T5 (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 (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2562643T5 (es) 2010-09-30 2019-05-24 Astrazeneca Ab Conjugado de naloxol-peg cristalino
MX367773B (es) * 2012-10-30 2019-09-05 Nektar Therapeutics Forma salina sólida de la alfa-6-mpeg6-o-hidroxicodona como agonistas opioides y sus usos.
SG11201707350TA (en) * 2015-03-10 2017-10-30 Rhodes Tech Acetate salt of buprenorphine and methods for preparing buprenorphine
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
EP3544590A4 (en) 2016-11-23 2020-10-28 Aurobindo Pharma Limited NALOXEGOL OXALATE AND SOLID DISPERSION OF IT
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
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
WO1994006426A1 (en) * 1992-09-21 1994-03-31 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
KR100653153B1 (ko) 1999-12-22 2006-12-01 넥타르 테라퓨틱스 에이엘, 코포레이션 수용성 중합체의 입체장애 유도체
US6413507B1 (en) 1999-12-23 2002-07-02 Shearwater Corporation Hydrolytically degradable carbamate derivatives of poly (ethylene glycol)
AU2001257577A1 (en) 2000-02-28 2001-09-03 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
WO2002043772A2 (en) 2000-11-30 2002-06-06 Shearwater Corporation Water-soluble polymer conjugates of triazine derivatives
ES2270955T3 (es) 2000-12-22 2007-04-16 Smithkline Beecham Plc Sal mesilato de 5-(4-(2-(n-metil-n-(2-piridil)amino)etoxi)bencil)tiazolidina-2,4-diona.
WO2002065988A2 (en) 2001-02-20 2002-08-29 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
DK2939696T3 (en) 2001-10-18 2016-05-23 Nektar Therapeutics Polymer Conjugates of Opioid Antagonists
MXPA04004026A (es) 2001-10-29 2004-07-08 Nektar Therapeutics Al Corp Conjugados polimericos de inhibidores de la proteina quinasa c.
ATE359829T1 (de) 2001-10-30 2007-05-15 Nektar Therapeutics Al Corp Wasserlösliche polymerkonjugate von retinoesäure
DK2425821T5 (en) 2002-04-05 2018-02-12 Mundipharma As Pharmaceutical preparation containing oxycodone and naloxone
GB0317815D0 (en) 2003-07-30 2003-09-03 Amersham Health As Imaging agents
US7405198B2 (en) 2003-11-24 2008-07-29 Neose Technologies, Inc. Glycopegylated erythropoietin
DK1694363T3 (en) 2003-12-16 2014-03-24 Nektar Therapeutics Monodisperse PEGylated Naloxole Compositions
US20060182692A1 (en) 2003-12-16 2006-08-17 Fishburn C S Chemically modified small molecules
US8320574B2 (en) * 2006-04-20 2012-11-27 Hewlett-Packard Development Company, L.P. Methods and systems for reducing acoustic echoes in communication systems
EP2010539B1 (en) 2006-04-21 2017-06-14 Nektar Therapeutics Stereoselective reduction of a morphinone
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
EA201001643A1 (ru) * 2008-05-07 2011-06-30 Нектар Терапеутикс Пероральное введение периферически действующих опиоидных антагонистов
CA2768392C (en) 2009-07-21 2018-04-17 Nektar Therapeutics Oligomer-opioid agonist conjugates
ES2562643T5 (es) 2010-09-30 2019-05-24 Astrazeneca Ab Conjugado de naloxol-peg cristalino

Also Published As

Publication number Publication date
US20150038524A1 (en) 2015-02-05
UA112847C2 (uk) 2016-11-10
EP2621496A1 (en) 2013-08-07
ES2562643T5 (es) 2019-05-24
TWI518088B (zh) 2016-01-21
RS54488B1 (en) 2016-06-30
ES2562643T8 (es) 2022-07-12
BR112013007113A2 (pt) 2017-07-25
SMT201600004B (it) 2016-02-25
GT201300084A (es) 2015-01-16
EA023929B1 (ru) 2016-07-29
KR20130135844A (ko) 2013-12-11
CU20130047A7 (es) 2013-08-29
PL2621496T3 (pl) 2016-05-31
PE20140636A1 (es) 2014-06-18
AR083268A1 (es) 2013-02-13
EP2621496A4 (en) 2014-09-24
SG188474A1 (en) 2013-05-31
RS54488B8 (sr) 2022-11-30
HK1187248A1 (zh) 2014-04-04
HRP20151420T4 (hr) 2019-04-05
MX2013003587A (es) 2013-05-31
IL225308A0 (en) 2013-06-27
MY173890A (en) 2020-02-26
JP2013538849A (ja) 2013-10-17
CA2812649A1 (en) 2012-04-05
CL2013000866A1 (es) 2013-08-30
KR101791724B1 (ko) 2017-10-30
SI2621496T2 (sl) 2019-04-30
CO6700851A2 (es) 2013-06-28
JP6034789B2 (ja) 2016-11-30
US9149539B1 (en) 2015-10-06
EP2621496B1 (en) 2015-12-16
CU24317B1 (es) 2018-02-08
NZ609874A (en) 2014-10-31
EP2621496B2 (en) 2018-12-12
UY33643A (es) 2012-04-30
AU2011307608A8 (en) 2015-08-27
EP2992903A1 (en) 2016-03-09
PH12013500561A1 (en) 2013-06-10
ES2819305T3 (es) 2021-04-15
CN103237547A (zh) 2013-08-07
DK2621496T4 (en) 2019-03-18
ECSP13012531A (es) 2013-06-28
EP2992903B1 (en) 2020-07-15
WO2012044243A1 (en) 2012-04-05
ES2819305T8 (es) 2022-05-26
NI201300034A (es) 2014-01-23
SI2621496T1 (sl) 2016-02-29
RS54488B2 (sr) 2019-03-29
KR101791724B9 (ko) 2022-06-16
AU2011307608B2 (en) 2015-04-09
TW201307356A (zh) 2013-02-16
PT2621496E (pt) 2016-02-01
SA111320808B1 (ar) 2014-12-15
CN103237547B (zh) 2015-10-07
ME02313B (me) 2016-06-20
EP2992903B8 (en) 2022-06-08
HRP20151420T1 (hr) 2016-01-29
US20150283257A1 (en) 2015-10-08
US9012469B2 (en) 2015-04-21
EA201300423A1 (ru) 2013-09-30
CR20130146A (es) 2013-05-15
HUE026726T2 (en) 2016-07-28
AU2011307608A1 (en) 2013-05-02
DK2621496T3 (en) 2016-01-18
ES2562643T3 (es) 2016-03-07
BR112013007113B1 (pt) 2020-09-24
AU2011307608B8 (en) 2015-08-27
PL2621496T5 (pl) 2019-05-31

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