SG11201407337QA - Cyclodextrin complexation methods for formulating peptide proteasome inhibitors - Google Patents

Cyclodextrin complexation methods for formulating peptide proteasome inhibitors

Info

Publication number
SG11201407337QA
SG11201407337QA SG11201407337QA SG11201407337QA SG11201407337QA SG 11201407337Q A SG11201407337Q A SG 11201407337QA SG 11201407337Q A SG11201407337Q A SG 11201407337QA SG 11201407337Q A SG11201407337Q A SG 11201407337QA SG 11201407337Q A SG11201407337Q A SG 11201407337QA
Authority
SG
Singapore
Prior art keywords
international
lllll
proteasome inhibitors
methods
llll
Prior art date
Application number
SG11201407337QA
Other languages
English (en)
Inventor
Evan Lewis
Peter Shwonek
Sean Dalziel
Mouhannad Jumaa
Original Assignee
Onyx Therapeutics Inc
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=48326170&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SG11201407337Q(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Onyx Therapeutics Inc filed Critical Onyx Therapeutics Inc
Publication of SG11201407337QA publication Critical patent/SG11201407337QA/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/19Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles lyophilised, i.e. freeze-dried, solutions or dispersions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/04Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • A61K38/07Tetrapeptides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/55Protease inhibitors
    • 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
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/36Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
    • A61K47/40Cyclodextrins; Derivatives 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
    • A61K47/69Medicinal 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 conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
    • A61K47/6949Medicinal 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 conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes
    • A61K47/6951Medicinal 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 conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes using cyclodextrin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0019Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y5/00Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S530/00Chemistry: natural resins or derivatives; peptides or proteins; lignins or reaction products thereof
    • Y10S530/827Proteins from mammals or birds
    • Y10S530/829Blood

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Nanotechnology (AREA)
  • Immunology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Biotechnology (AREA)
  • General Engineering & Computer Science (AREA)
  • Medical Informatics (AREA)
  • Molecular Biology (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Biophysics (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Dermatology (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
SG11201407337QA 2012-05-08 2013-05-08 Cyclodextrin complexation methods for formulating peptide proteasome inhibitors SG11201407337QA (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201261644122P 2012-05-08 2012-05-08
US201361777475P 2013-03-12 2013-03-12
PCT/US2013/040127 WO2013169897A1 (en) 2012-05-08 2013-05-08 Cylodextrin complexation methods for formulating peptide proteasome inhibitors

Publications (1)

Publication Number Publication Date
SG11201407337QA true SG11201407337QA (en) 2014-12-30

Family

ID=48326170

Family Applications (2)

Application Number Title Priority Date Filing Date
SG11201407337QA SG11201407337QA (en) 2012-05-08 2013-05-08 Cyclodextrin complexation methods for formulating peptide proteasome inhibitors
SG10201609318UA SG10201609318UA (en) 2012-05-08 2013-05-08 Cyclodextrin complexation methods for formulating peptide proteasome inhibitors

Family Applications After (1)

Application Number Title Priority Date Filing Date
SG10201609318UA SG10201609318UA (en) 2012-05-08 2013-05-08 Cyclodextrin complexation methods for formulating peptide proteasome inhibitors

Country Status (24)

Country Link
US (1) US10159746B2 (de)
EP (2) EP4410374A2 (de)
JP (1) JP6410264B2 (de)
KR (5) KR20240119191A (de)
CN (2) CN104411334A (de)
AU (2) AU2013259573B2 (de)
CA (1) CA2873044C (de)
CL (1) CL2014003055A1 (de)
DK (1) DK2662094T3 (de)
EA (1) EA033614B1 (de)
ES (1) ES2981576T3 (de)
FI (1) FI2662094T3 (de)
HK (2) HK1207827A1 (de)
HR (1) HRP20240724T1 (de)
HU (1) HUE066956T2 (de)
IL (1) IL235553B (de)
LT (1) LT2662094T (de)
MX (2) MX364393B (de)
PL (1) PL2662094T3 (de)
PT (1) PT2662094T (de)
RS (1) RS65647B1 (de)
SG (2) SG11201407337QA (de)
SI (1) SI2662094T1 (de)
WO (1) WO2013169897A1 (de)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015009888A2 (en) 2013-07-19 2015-01-22 Onyx Therapeutics, Inc. Peptide epoxyketone proteasome inhibitors in combination with pim kinase inhibitors for treatment of cancers
CN104945470B (zh) * 2014-03-30 2020-08-11 浙江大学 杂环构建的三肽环氧酮类化合物及制备和应用
KR102655020B1 (ko) 2016-06-29 2024-04-04 케자르 라이프 사이언스 펩티드 에폭시케톤 면역프로테아좀 억제제의 결정질 염
EA201990157A1 (ru) 2016-06-29 2019-05-31 Кезар Лайф Сайнсиз Способ получения пептидного эпоксикетонового ингибитора иммунопротеасомы и его предшественников
WO2018038687A1 (en) 2016-08-22 2018-03-01 Mustafa Nevzat Ilaç Sanayii A.Ş. Pharmaceutical formulations comprising a bortezomib-cyclodextrin complex
TWI773706B (zh) * 2016-11-29 2022-08-11 瑞士商歐庫利斯公司 用於眼用活性藥物成分輸送的固體環糊精複合物之製備
AU2018263924B2 (en) * 2017-05-03 2024-07-04 Cydex Pharmaceuticals, Inc. Composition containing cyclodextrin and busulfan
EP3993807A1 (de) 2019-07-01 2022-05-11 Oculis SA Verfahren zur stabilisierung des ph einer wässrigen zusammensetzung mit einem arzneimittel
CN110882221B (zh) * 2019-11-29 2021-06-29 健进制药有限公司 一种注射用卡非佐米冻干制剂的生产工艺
WO2022159319A2 (en) * 2021-01-19 2022-07-28 Mountain Valley Md Inc A porous aluminum nanoparticulate structure

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4522811A (en) 1982-07-08 1985-06-11 Syntex (U.S.A.) Inc. Serial injection of muramyldipeptides and liposomes enhances the anti-infective activity of muramyldipeptides
US5340736A (en) 1991-05-13 1994-08-23 The President & Fellows Of Harvard College ATP-dependent protease and use of inhibitors for same in the treatment of cachexia and muscle wasting
US5858784A (en) 1991-12-17 1999-01-12 The Regents Of The University Of California Expression of cloned genes in the lung by aerosol- and liposome-based delivery
DE19505263A1 (de) * 1995-02-16 1996-08-22 Consortium Elektrochem Ind Verfahren zur Reinigung von wasserlöslichen Cyclodextrinderivaten
WO1998010779A1 (en) 1996-09-13 1998-03-19 New York University Method for treating parasitic diseases with proteasome inhibitors
US6042820A (en) 1996-12-20 2000-03-28 Connaught Laboratories Limited Biodegradable copolymer containing α-hydroxy acid and α-amino acid units
GB9713149D0 (en) 1997-06-21 1997-08-27 Pfizer Ltd Pharmaceutical formulations
PT889056E (pt) 1997-07-01 2006-07-31 Pfizer Prod Inc Processo para produzir um,a ciclodextrina.
US6472375B1 (en) 1998-04-16 2002-10-29 John Wayne Cancer Institute DNA vaccine and methods for its use
US6831099B1 (en) 1999-05-12 2004-12-14 Yale University Enzyme inhibition
DE50110956D1 (de) 2000-10-12 2006-10-19 Viromics Gmbh Proteasome inhibitoren zur behandlung von hepatitis-virus infektionen
NZ548225A (en) * 2003-12-31 2012-12-21 Cydex Pharmaceuticals Inc Inhalant formulation containing sulfoakyl ether cyclodextrin and corticosteroid
US7232818B2 (en) 2004-04-15 2007-06-19 Proteolix, Inc. Compounds for enzyme inhibition
CN102174076A (zh) 2004-04-15 2011-09-07 普罗特奥里克斯公司 用于抑制蛋白酶体酶的化合物
DK1819353T3 (da) * 2004-12-07 2011-05-16 Proteolix Inc Sammensætning til proteasomhæmning
BRPI0618653A2 (pt) * 2005-11-15 2011-09-06 Baxter Int composições compreendendo inibidores da lipoxigenase e ciclodextrina
KR20150131405A (ko) * 2007-10-04 2015-11-24 오닉스 세라퓨틱스, 인크. 결정형 펩티드 에폭시 케톤 프로테아제 저해제 및 아미노산 케토-에폭시드의 합성
US7635773B2 (en) 2008-04-28 2009-12-22 Cydex Pharmaceuticals, Inc. Sulfoalkyl ether cyclodextrin compositions
EP2349313A4 (de) 2008-10-21 2012-08-29 Onyx Therapeutics Inc Kombinationstherapie mit peptidepoxyketonen
KR20200106100A (ko) 2012-02-28 2020-09-10 사이덱스 파마슈티칼스, 인크. 알킬화된 시클로덱스트린 조성물 및 이의 제조 및 사용 방법

Also Published As

Publication number Publication date
HK1207827A1 (en) 2016-02-12
JP6410264B2 (ja) 2018-10-24
SG10201609318UA (en) 2016-12-29
IL235553A0 (en) 2015-01-29
MX2014013552A (es) 2015-05-08
MX364393B (es) 2019-04-24
CA2873044A1 (en) 2013-11-14
KR20150008165A (ko) 2015-01-21
PT2662094T (pt) 2024-07-04
HRP20240724T1 (hr) 2024-08-30
DK2662094T3 (da) 2024-07-08
RS65647B1 (sr) 2024-07-31
CN104411334A (zh) 2015-03-11
EA201491994A1 (ru) 2015-04-30
EP4410374A2 (de) 2024-08-07
HUE066956T2 (hu) 2024-09-28
CN107693772A (zh) 2018-02-16
IL235553B (en) 2018-04-30
KR102054329B1 (ko) 2019-12-10
AU2013259573A1 (en) 2014-11-27
KR20220088949A (ko) 2022-06-28
PL2662094T3 (pl) 2024-08-05
JP2015516430A (ja) 2015-06-11
EP2662094A1 (de) 2013-11-13
AU2018200444A1 (en) 2018-02-08
US20150111838A1 (en) 2015-04-23
CA2873044C (en) 2021-01-26
ES2981576T3 (es) 2024-10-09
SI2662094T1 (sl) 2024-09-30
AU2018200444B2 (en) 2019-10-31
CL2014003055A1 (es) 2015-02-13
EA033614B1 (ru) 2019-11-11
KR20190137963A (ko) 2019-12-11
HK1250927A1 (zh) 2019-01-18
KR20240119191A (ko) 2024-08-06
LT2662094T (lt) 2024-07-10
KR20200130748A (ko) 2020-11-19
US10159746B2 (en) 2018-12-25
AU2013259573B2 (en) 2018-02-15
FI2662094T3 (fi) 2024-06-26
EP2662094B1 (de) 2024-04-17
MX2019004845A (es) 2021-03-31
WO2013169897A1 (en) 2013-11-14

Similar Documents

Publication Publication Date Title
SG11201407337QA (en) Cyclodextrin complexation methods for formulating peptide proteasome inhibitors
SG11201804170RA (en) Polycyclic tlr7/8 antagonists and use thereof in the treatment of immune disorders
SG11201810983PA (en) Novel heterocyclic derivatives useful as shp2 inhibitors
SG11201808682XA (en) Silicone atoms containing ivacaftor analogues
SG11201808990QA (en) Compositions for topical application of compounds
SG11201805645QA (en) Lsd1 inhibitors
SG11201408769QA (en) Methods of reducing the risk of a cardiovascular event in a subject on statin therapy
SG11201805300QA (en) Heterocyclic compounds as immunomodulators
SG11201803920TA (en) Compounds and compositions useful for treating disorders related to ntrk
SG11201806583XA (en) Compositions containing tucaresol or its analogs
SG11201408739VA (en) Inhibitors of hepatitis c virus
SG11201408094YA (en) Neprilysin inhibitors
SG11201805380YA (en) Urea-based prostate specific membrane antigen (psma) inhibitors for imaging and therapy
CA2859619C (en) Bromodomain inhibitors
SG11201407200TA (en) Liquid formulation
SG11201407228PA (en) N-aryltriazole compounds as lpar antagonists
SG11201407580YA (en) Composition comprising two antibodies engineered to have reduced and increased effector function
SG11201408174UA (en) Antibody formulation
SG11201408539UA (en) Enhancing autophagy or increasing longevity by administration of urolithins or precursors thereof
SG11201407220YA (en) N-alkyltriazole compounds as lpar antagonists
SG11201809499UA (en) Processes for preparing phosphorodiamidate morpholino oligomers
SG11201811416VA (en) Crystalline solid forms of a bet inhibitor
SG11201809497RA (en) Processes for preparing phosphorodiamidate morpholino oligomers
SG11201402986RA (en) Kinase inhibitors
SG11201900405XA (en) Compounds, compositions and methods for treating or preventing a sympton associated with gout or hyperuricemia