ATE304356T1 - Zusammenstellungen zur krebsbehandlung - Google Patents

Zusammenstellungen zur krebsbehandlung

Info

Publication number
ATE304356T1
ATE304356T1 AT02011928T AT02011928T ATE304356T1 AT E304356 T1 ATE304356 T1 AT E304356T1 AT 02011928 T AT02011928 T AT 02011928T AT 02011928 T AT02011928 T AT 02011928T AT E304356 T1 ATE304356 T1 AT E304356T1
Authority
AT
Austria
Prior art keywords
disease
sarcoma
cancer treatment
treatment compositions
treating
Prior art date
Application number
AT02011928T
Other languages
German (de)
English (en)
Inventor
Amato Robert D
Original Assignee
Childrens Medical Center
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=26699202&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ATE304356(T1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Childrens Medical Center filed Critical Childrens Medical Center
Application granted granted Critical
Publication of ATE304356T1 publication Critical patent/ATE304356T1/de

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19—Carboxylic acids, e.g. valproic acid
    • A—HUMAN NECESSITIES
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
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    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/4035—Isoindoles, e.g. phthalimide
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    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
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    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
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    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
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    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Oncology (AREA)
  • Immunology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Diabetes (AREA)
  • Communicable Diseases (AREA)
  • Hematology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Virology (AREA)
  • Rheumatology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Dermatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Vascular Medicine (AREA)
  • Emergency Medicine (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Pain & Pain Management (AREA)
  • Urology & Nephrology (AREA)
  • Molecular Biology (AREA)
  • Biotechnology (AREA)
  • Obesity (AREA)
  • Endocrinology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
AT02011928T 1993-03-01 1994-02-24 Zusammenstellungen zur krebsbehandlung ATE304356T1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US2504693A 1993-03-01 1993-03-01
US08/168,817 US5629327A (en) 1993-03-01 1993-12-15 Methods and compositions for inhibition of angiogenesis

Publications (1)

Publication Number Publication Date
ATE304356T1 true ATE304356T1 (de) 2005-09-15

Family

ID=26699202

Family Applications (2)

Application Number Title Priority Date Filing Date
AT02011928T ATE304356T1 (de) 1993-03-01 1994-02-24 Zusammenstellungen zur krebsbehandlung
AT94909773T ATE218865T1 (de) 1993-03-01 1994-02-24 Thalidomid zur hemmung der angiogenese

Family Applications After (1)

Application Number Title Priority Date Filing Date
AT94909773T ATE218865T1 (de) 1993-03-01 1994-02-24 Thalidomid zur hemmung der angiogenese

Country Status (20)

Country Link
US (18) US5629327A (US20020061911A1-20020523-C00002.png)
EP (4) EP1537870A3 (US20020061911A1-20020523-C00002.png)
JP (4) JPH08507767A (US20020061911A1-20020523-C00002.png)
KR (1) KR100506043B1 (US20020061911A1-20020523-C00002.png)
AT (2) ATE304356T1 (US20020061911A1-20020523-C00002.png)
AU (1) AU676722B2 (US20020061911A1-20020523-C00002.png)
BR (1) BR9400764A (US20020061911A1-20020523-C00002.png)
CA (3) CA2342974C (US20020061911A1-20020523-C00002.png)
CO (1) CO4230017A1 (US20020061911A1-20020523-C00002.png)
DE (3) DE69434490T2 (US20020061911A1-20020523-C00002.png)
DK (2) DK0688211T3 (US20020061911A1-20020523-C00002.png)
ES (2) ES2245711T3 (US20020061911A1-20020523-C00002.png)
FR (1) FR08C0036I2 (US20020061911A1-20020523-C00002.png)
HK (1) HK1052865A1 (US20020061911A1-20020523-C00002.png)
LU (1) LU91471I2 (US20020061911A1-20020523-C00002.png)
NL (1) NL300358I2 (US20020061911A1-20020523-C00002.png)
NZ (4) NZ262676A (US20020061911A1-20020523-C00002.png)
PE (1) PE10095A1 (US20020061911A1-20020523-C00002.png)
PT (1) PT688211E (US20020061911A1-20020523-C00002.png)
WO (1) WO1994020085A1 (US20020061911A1-20020523-C00002.png)

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US6582959B2 (en) 1991-03-29 2003-06-24 Genentech, Inc. Antibodies to vascular endothelial cell growth factor
US8143283B1 (en) * 1993-03-01 2012-03-27 The Children's Medical Center Corporation Methods for treating blood-born tumors with thalidomide
US5629327A (en) * 1993-03-01 1997-05-13 Childrens Hospital Medical Center Corp. Methods and compositions for inhibition of angiogenesis
US6114355A (en) * 1993-03-01 2000-09-05 D'amato; Robert Methods and compositions for inhibition of angiogenesis
US6228879B1 (en) 1997-10-16 2001-05-08 The Children's Medical Center Methods and compositions for inhibition of angiogenesis
US20040248799A1 (en) * 1993-05-27 2004-12-09 Holaday John W. Compositions and methods for treating cancer and hyperproliferative disorders
US6805865B1 (en) 1993-05-27 2004-10-19 Entremed, Inc. Compositions and methods for treating cancer and hyperproliferative disorders
DE4422237A1 (de) 1994-06-24 1996-01-04 Gruenenthal Gmbh Verwendung von Lactamverbindungen als pharmazeutische Wirkstoffe
US6429221B1 (en) * 1994-12-30 2002-08-06 Celgene Corporation Substituted imides
US6358735B1 (en) 1995-06-30 2002-03-19 University Of Kansas Medical Center Method for inhibiting angiogenesis and tumors with the isolated NC1 α3 chain monomer of type IV collagen
US6440729B1 (en) 1995-06-30 2002-08-27 University Of Kansas Medical Center Treating angiogenesis-mediated diseases with the α2 monomer of type IV collagen
US6518281B2 (en) * 1995-08-29 2003-02-11 Celgene Corporation Immunotherapeutic agents
US6346510B1 (en) 1995-10-23 2002-02-12 The Children's Medical Center Corporation Therapeutic antiangiogenic endostatin compositions
JP3263598B2 (ja) * 1995-11-01 2002-03-04 有限会社ドット 経鼻吸収用生理活性ペプチド組成物
EP2177517B1 (en) * 1996-07-24 2011-10-26 Celgene Corporation Amino substituted 2-(2,6-dioxopiperidin-3-yl)-phthalimide for reducing TNF alpha levels
DE122007000079I2 (de) * 1996-07-24 2010-08-12 Celgene Corp Substituierte 2-(2,6-dioxopiperidin-3-yl)-phthalimide und -1-oxoisoindoline und verfahren zur reduzierung des tnf-alpha-spiegels
US5635517B1 (en) * 1996-07-24 1999-06-29 Celgene Corp Method of reducing TNFalpha levels with amino substituted 2-(2,6-dioxopiperidin-3-YL)-1-oxo-and 1,3-dioxoisoindolines
US5798368A (en) * 1996-08-22 1998-08-25 Celgene Corporation Tetrasubstituted 2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolines and method of reducing TNFα levels
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BR9400764A (pt) 1994-11-01
FR08C0036I1 (US20020061911A1-20020523-C00002.png) 2008-10-17
US8012996B2 (en) 2011-09-06
DE122008000044I2 (US20020061911A1-20020523-C00002.png) 2010-12-30
US5629327A (en) 1997-05-13
WO1994020085A1 (en) 1994-09-15
EP1245229A2 (en) 2002-10-02
CA2342974A1 (en) 1994-09-15
EP1537870A3 (en) 2007-12-12
ES2245711T3 (es) 2006-01-16
JP2008088182A (ja) 2008-04-17
US5593990A (en) 1997-01-14
JP2001278789A (ja) 2001-10-10
US6235756B1 (en) 2001-05-22
EP1245229A3 (en) 2004-05-06
KR960701632A (ko) 1996-03-28
US6071948A (en) 2000-06-06
US20030176463A1 (en) 2003-09-18
CA2342974C (en) 2005-08-16
FR08C0036I2 (US20020061911A1-20020523-C00002.png) 2009-11-20
CA2157288A1 (en) 1994-09-15
US20020052398A1 (en) 2002-05-02
JP2004359693A (ja) 2004-12-24
NZ262676A (en) 1999-08-30
CA2157288C (en) 2005-11-08
PE10095A1 (es) 1995-04-25
NZ336527A (en) 2005-01-28
US6420414B1 (en) 2002-07-16
JP4065373B2 (ja) 2008-03-26
NZ535670A (en) 2006-05-26
HK1052865A1 (en) 2003-10-03
AU676722B2 (en) 1997-03-20
NL300358I1 (nl) 2008-11-03

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