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IMS Company Profiles - Report Buyer

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<strong>IMS</strong> COM PANY PRO FILES TAKEDA<br />

Product Class Date Terms of Agreement<br />

Omacor (TAK 085) A 2005 Takeda licensed the Japanese rights to Omacor from<br />

Pronova.<br />

Matuzumab L 2005 Takeda signed a co-development and co-promotion<br />

agreement for matuzumab with originator Merck KGaA in<br />

September 2005.<br />

Ilaprazole A 2005 Il Yang licensed worldwide rights to ilaprazole, a proton<br />

pump inhibitor, outside South Korea and China, to TAP.<br />

R 851 J 2005 Collaboration to jointly develop and market 3Ms topical<br />

immune response modifier. Takeda has acquired<br />

exclusive Japan/Asia region rights. In 2007 this<br />

agreement was updated granting Takeda full rights to the<br />

drug from 3M.<br />

GnRH analogue, Norwood<br />

Immunology/TAP<br />

L 2005 TAP and Norwood Immunology are jointly developing<br />

GnRH analogues, which have potential in bone marrow<br />

transplants, cancer and HIV infection.<br />

TAK 363/TRK 130 G 2005 A compound for the treatment of urinary incontinence,<br />

co-developed by Takeda and Toray. Toray will market it<br />

in Japan and Takeda will market it in overseas territories.<br />

It was discovered in Toray’s compound library through<br />

joint research by both companies<br />

Idebenone N 2005 Collaborative deal with regarding development of<br />

Santhera’s idebenone, a small molecule with potential in<br />

the treatment of Friedreich’s ataxia. Santhera will<br />

conduct all clinical development to gain regulatory<br />

approval in Europe and the USA. Takeda will support<br />

development and obtain an exclusive marketing license in<br />

the EU and Switzerland. Santhera plans to market<br />

idebenone independently in the USA. In August 2007<br />

Santhera granted Takeda marketing rights in the EU and<br />

Switzerland to idebenone for the treatment of Duchenne<br />

Muscular Dystrophy (DMD).<br />

Amitiza (lubiprostone) A 2004 Takeda agreed to jointly market lubiprostone in the USA<br />

and Canada with originator Sucampo Takeda also<br />

acquired an option to lubipristone in other territories,<br />

such as Japan and Europe.<br />

Arxxant (ruboxistaurin) A 2003 Takeda signed an agreement with Lilly for joint<br />

development and co-marketing of the product in Japan.<br />

cetilistat (ATL 962) A 2003 Alizyme granted Takeda exclusive rights to develop,<br />

manufacture and market in Japan.<br />

© 2009 <strong>IMS</strong> Health In cor po rated or its af fil i ates Page 97

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