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WO2004024089A3 - Inhibition or activation of adam9 and adam15 for treatment of vascularization-related disease and wound healing - Google Patents

Inhibition or activation of adam9 and adam15 for treatment of vascularization-related disease and wound healing Download PDF

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Publication number
WO2004024089A3
WO2004024089A3 PCT/US2003/028751 US0328751W WO2004024089A3 WO 2004024089 A3 WO2004024089 A3 WO 2004024089A3 US 0328751 W US0328751 W US 0328751W WO 2004024089 A3 WO2004024089 A3 WO 2004024089A3
Authority
WO
WIPO (PCT)
Prior art keywords
adam
adam9
adam15
neovascularization
inhibition
Prior art date
Application number
PCT/US2003/028751
Other languages
French (fr)
Other versions
WO2004024089A2 (en
Inventor
Carl P Blobel
Keisuke Horiuchi
Gisela Weskamp
Klaus Preissner
Original Assignee
Sloan Kettering Inst Cancer
Univ Mannheim Heidelberg
Univ Giessen Justus Liebig
Carl P Blobel
Keisuke Horiuchi
Gisela Weskamp
Hammes Hans Peter
Klaus Preissner
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
Application filed by Sloan Kettering Inst Cancer, Univ Mannheim Heidelberg, Univ Giessen Justus Liebig, Carl P Blobel, Keisuke Horiuchi, Gisela Weskamp, Hammes Hans Peter, Klaus Preissner filed Critical Sloan Kettering Inst Cancer
Priority to AU2003270625A priority Critical patent/AU2003270625A1/en
Publication of WO2004024089A2 publication Critical patent/WO2004024089A2/en
Publication of WO2004024089A3 publication Critical patent/WO2004024089A3/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4406Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 3, e.g. zimeldine

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)

Abstract

Inhibition of neovascularization is achieved by exposing a tissue susceptible to neovascularization to a therapeutic agent effective to inhibit ADAM 9 and/or ADAM 15. The therapeutic agent may be, for example, an antibody, a small molecule therapeutic, an antisense or RNAi therapeutic, or an agent for introducing targeted mutations in the genetic sequence for ADAM9 and/or ADAM 15. Thus, an individual suffering from a condition associated with pathological neovascularization is treated by administration of a therapeutic agent effective to inhibit a ADAM 9 or ADAM 15. Activation of ADAM9 or ADAM 15 can be used for promotion of neovascularization, for example to facilitate wound healing, perfusion or circulation. In this case, the therapeutic agent used is one which enhances the active amount of ADAM9 and/or ADAM15. Inhibition or activation of ADAM9 and/or ADAM15 in accordance with the methods of the invention provides an attractive alternative to targeting of other ADAM species, such as ADAM10, because neither ADAM9 nor ADAM15 appears to be essential for development or maintenance. Thus, side effects are minimised.
PCT/US2003/028751 2002-09-11 2003-09-11 Inhibition or activation of adam9 and adam15 for treatment of vascularization-related disease and wound healing WO2004024089A2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU2003270625A AU2003270625A1 (en) 2002-09-11 2003-09-11 Inhibition or activation of adam9 and adam15 for treatment of vascularization-related disease and wound healing

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US40985802P 2002-09-11 2002-09-11
US60/409858 2002-09-11

Publications (2)

Publication Number Publication Date
WO2004024089A2 WO2004024089A2 (en) 2004-03-25
WO2004024089A3 true WO2004024089A3 (en) 2005-02-03

Family

ID=31994015

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2003/028751 WO2004024089A2 (en) 2002-09-11 2003-09-11 Inhibition or activation of adam9 and adam15 for treatment of vascularization-related disease and wound healing

Country Status (2)

Country Link
AU (1) AU2003270625A1 (en)
WO (1) WO2004024089A2 (en)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7309487B2 (en) * 2004-02-09 2007-12-18 George Inana Methods and compositions for detecting and treating retinal diseases
MX2007009222A (en) * 2005-02-02 2008-01-16 Raven Biotechnologies Inc Adam-9 modulators.
EP2243488B1 (en) * 2006-01-19 2013-08-14 Eyegene Inc. Pharmaceutical composition for treating vascular-related diseases comprising peptide
GB2453589A (en) * 2007-10-12 2009-04-15 King S College London Protease inhibition
CN101946003B (en) * 2008-02-14 2013-05-15 株式会社遗传科技 Anti-adam-15 antibodies and utilization of the same
WO2009118660A2 (en) * 2008-03-24 2009-10-01 Salman Rahman Adam-15 antibodies and immunogenic peptides
JP2012517821A (en) * 2009-02-19 2012-08-09 ガラパゴス・ナムローゼ・フェンノートシャップ Identification method and compound useful for diagnosis and treatment of diseases including inflammation
US9732157B2 (en) 2010-10-01 2017-08-15 Salman Rahman Methods for the development of metzincin-selective catalytic cleft directed antibodies for therapeutic and diagnostic applications
EP3700521B1 (en) 2017-10-29 2024-06-12 China Medical University Use of adam9 inhibitor compound and composition including adam9 inhibitor compound
TWI735210B (en) * 2019-04-26 2021-08-01 中國醫藥大學 Use of adam9 inhibitor as immune modulator
CN114578052A (en) * 2022-03-08 2022-06-03 新疆医科大学第一附属医院 Application of ADAM10 in occlusive cardiovascular and cerebrovascular diseases

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6465468B1 (en) * 1999-03-22 2002-10-15 Darwin Discovery Limited Hydroxamic and carboxylic acid derivatives

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6465468B1 (en) * 1999-03-22 2002-10-15 Darwin Discovery Limited Hydroxamic and carboxylic acid derivatives

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
ROGHANI ET AL: "Metalloprotease-Disintergrin MDC 9: Intracellular maturation and catalytic activity", J. OF BIO. CHEM., vol. 274, no. 6, 1999, pages 3531 - 3540, XP000919470 *

Also Published As

Publication number Publication date
AU2003270625A1 (en) 2004-04-30
WO2004024089A2 (en) 2004-03-25
AU2003270625A8 (en) 2004-04-30

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