JP2012526798A5 - - Google Patents

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Publication number
JP2012526798A5
JP2012526798A5 JP2012510440A JP2012510440A JP2012526798A5 JP 2012526798 A5 JP2012526798 A5 JP 2012526798A5 JP 2012510440 A JP2012510440 A JP 2012510440A JP 2012510440 A JP2012510440 A JP 2012510440A JP 2012526798 A5 JP2012526798 A5 JP 2012526798A5
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JP
Japan
Prior art keywords
composition according
agonist
iop
meca
subject
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.)
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Application number
JP2012510440A
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English (en)
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JP2012526798A (ja
JP5849044B2 (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/IL2010/000393 external-priority patent/WO2010134067A1/en
Publication of JP2012526798A publication Critical patent/JP2012526798A/ja
Publication of JP2012526798A5 publication Critical patent/JP2012526798A5/ja
Application granted granted Critical
Publication of JP5849044B2 publication Critical patent/JP5849044B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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Claims (9)

  1. AR作動薬がIOPの被検者のIOPの低下に有効であり有効成分として前記AR作動薬および生理学的に許容される担体を含有する、前記被検者のIOPを低下させる医薬組成物。
  2. 前記被検者がヒト被検者である、請求項に記載に医薬組成物。
  3. 亢進したIOPを有する被験者のIOPを低下させるための、請求項1または2に記載の医薬組成物。
  4. 前記担体がA R作動薬の経口投与に好適である、請求項1から3のいずれか1項に記載の組成物。
  5. 1日2回の投与に好適な剤形で製剤された、請求項記載の組成物。
  6. 前記担体が前記 R作動薬の局所投与に好適である、請求項からいずれか1項に記載の組成物。
  7. 目に前記 R作動薬を投与するために製剤した、請求項記載の組成物。
  8. 前記A AR作動薬がN−2‐(4−アミノフェニル)エチルアデノシン(APNEA)、N‐(4‐アミノ‐3‐ヨードベンジル)‐アデノシン‐5’‐N‐メチルウロンアミド(AB−MECA)、N‐(3‐ヨードベンジル)‐アデノシン‐5’‐N‐メチルウロンアミド(IB‐MECA)および2−クロロ−N−(3−ヨードベンジル)−アデノシン‐5’‐N‐メチルウロンアミド(CI‐IB−MECA)からなる群から選択される、請求項1から7のいずれか1項に記載の組成物。
  9. 前記A AR作動薬がIB−MECAである、請求項記載の組成物。
JP2012510440A 2009-05-17 2010-05-16 眼圧低下のためのa3アデノシン受容体作動薬 Expired - Fee Related JP5849044B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
IL198787 2009-05-17
IL19878709 2009-05-17
PCT/IL2010/000393 WO2010134067A1 (en) 2009-05-17 2010-05-16 A3 adenosine receptor agonists for the reduction of intraocular pressure

Publications (3)

Publication Number Publication Date
JP2012526798A JP2012526798A (ja) 2012-11-01
JP2012526798A5 true JP2012526798A5 (ja) 2013-07-04
JP5849044B2 JP5849044B2 (ja) 2016-01-27

Family

ID=42352183

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2012510440A Expired - Fee Related JP5849044B2 (ja) 2009-05-17 2010-05-16 眼圧低下のためのa3アデノシン受容体作動薬

Country Status (10)

Country Link
US (1) US8557790B2 (ja)
EP (1) EP2432475A1 (ja)
JP (1) JP5849044B2 (ja)
KR (1) KR20120022919A (ja)
CN (1) CN102427819A (ja)
AU (1) AU2010250759B2 (ja)
CA (1) CA2761499A1 (ja)
IL (1) IL216114A (ja)
MX (1) MX2011012229A (ja)
WO (1) WO2010134067A1 (ja)

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5443836A (en) 1993-03-15 1995-08-22 Gensia, Inc. Methods for protecting tissues and organs from ischemic damage
AU7331094A (en) 1993-07-13 1995-02-13 United States Of America, As Represented By The Secretary, Department Of Health And Human Services, The A3 adenosine receptor agonists
US5688774A (en) 1993-07-13 1997-11-18 The United States Of America As Represented By The Department Of Health And Human Services A3 adenosine receptor agonists
AU1399297A (en) 1996-01-24 1997-08-20 Sumitomo Chemical Company, Limited Dihalopropene compounds, their use as insecticides/acaricides and intermediates for their production
US6048865A (en) 1997-07-29 2000-04-11 Medco Research, Inc. N6 -substituted-adenosine-5'-uronamides as adenosine receptor modulator
WO1999006053A1 (en) 1997-07-29 1999-02-11 Medco Research, Inc. N6-substituted-adenosine-5'-uronamides as adenosine receptor modulators
US6329349B1 (en) 1997-10-23 2001-12-11 Trustees Of The University Of Pennsylvania Methods for reducing ischemic injury of the heart via the sequential administration of monophosphoryl lipid A and adenosine receptor agents
US6217896B1 (en) 1999-04-01 2001-04-17 Uab Research Foundation Conjunctival inserts for topical delivery of medication or lubrication
IL133680A0 (en) 1999-09-10 2001-04-30 Can Fite Technologies Ltd Pharmaceutical compositions comprising an adenosine receptor agonist or antagonist
AU2003282359A1 (en) * 2002-11-19 2004-06-15 Can-Fite Biopharma Ltd. A3ar agonists for the treatment of inflammatory arthritis
BRPI0517639A (pt) * 2004-11-08 2008-10-14 Can Fite Biopharma Ltd método para o tratamento de ressorção óssea acelerada, composição farmacêutica, e, uso de um agonista de a3ar
CN101083998A (zh) * 2004-11-22 2007-12-05 王者制药研究发展有限公司 用腺苷a3受体激动剂强化治疗hif-1介导的病症
WO2007002139A2 (en) * 2005-06-22 2007-01-04 The Trustees Of The University Of Pennsylvania Neuroprotection of retinal ganglion cells
DK1983990T3 (da) * 2006-01-26 2011-07-11 Us Gov Health & Human Serv Allosteriske A3-adenosin-receptormodulatorer
BRPI0621052A2 (pt) * 2006-01-27 2012-07-17 Can Fite Biopharma Ltd uso de um agonista de receptor de adenosina a3 (a3ar)
US8153781B2 (en) * 2007-06-29 2012-04-10 The United States Of America As Represented By The Secretary, Department Of Health And Human Services Dendrimer conjugates of agonists and antagonists of the GPCR superfamily
EP3039030B1 (en) * 2013-08-29 2018-09-19 Yeda Research and Development Co. Ltd. Selective inhibitors of alpha2 isoform of na,k-atpase and use for reduction of intra-ocular pressure

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