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<strong>IMS</strong> COM PANY PRO FILES TAKEDA<br />
three years, but can be ex tended. If the com pa nies do not re new the part ner ship, Takeda will be el i gi ble<br />
to re ceive de clin ing tail pay ments for a pe riod of three years fol low ing 2006. Un der the agree ment,<br />
TPNA’s 1,000-strong US sales force will co-pro mote the prod ucts and Takeda will re ceive an un dis closed<br />
per cent age of net sales for the Kos’s (now Abbott’s) cur rent cho les terol franchise above a specific<br />
baseline level.<br />
Lifecycle Man age ment: Kos an nounced in July 2006 that it had sub mit ted a sup ple men tal NDA to the<br />
US FDA, seek ing the ap proval of a com plete dos age range of Niaspan CF, a caplet for mu la tion of the<br />
prod uct. The Niaspan CF range in cludes an op ti mized 1000mg caplet formulation.<br />
� Central Nervous System Agents<br />
ANPEC TAKEDA (mor phine hy dro chlo ride) was launched in Ja pan in 1991. It was co-launched with<br />
Tanab (now Mitsubishi Tanabe Pharm), Sankyo (now Daiichi Sankyo), Shionogi and Dainippon (now<br />
Dainippon Sumitomo, all Ja pan), which mar ket it as Anpec Tanabe, Anpec Sankyo etc. A con cen trated<br />
high-dose ver sion of mor phine hy dro chlo ride has been filed in Ja pan by Takeda and its joint de vel op ment<br />
part ners (with the lab o ra tory code MH 200), for the treat ment of se vere pain due to cancer.<br />
EURODIN (estazolam), an in ter me di ate-act ing benzo diaz epine, has been mar keted world wide for the<br />
short-term man age ment of in som nia since 1967. It was orig i nally de vel oped by the Takeda/Abbott joint<br />
ven ture, TAP (USA), dis solved in May 2008. In 2003, estazolam was launched in Tai wan, Rus sia and Lat -<br />
via as a treat ment for insomnia.<br />
HIRTONIN (protirelin), a thyrotropin-re leas ing hor mone, has been on the mar ket for some years as a<br />
di ag nos tic and ther a peu tic agent and was launched by Takeda in Ja pan as Hirtonin in 1978 as a<br />
nootropic. In 1988, Takeda Italia launched it as a nootropic un der the name Irtonin.<br />
MS CONTIN TAKEDA (mor phine sul fate) is a slow-re lease mor phine prod uct, orig i nally de vel oped by<br />
Mundipharma (Swit zer land). It was li censed out to Takeda for Ja pan and launched there in 1989. It was<br />
co-de vel oped with Tanabe (now Mitsubishi Tanabe Pharma), Sankyo (now Daiichi Sankyo), Shionogi and<br />
Dainippon (now Dainippon Sumitomo), which co-mar ket the prod uct in Ja pan as MS Contin Tanabe,<br />
MS Contin Sankyo etc. A high-dose con cen trated ver sion was launched in Japan in 1995.<br />
NICHOLIN (citicoline), an oral neuroprotective is avail able in more than 70 coun tries for the treat ment<br />
of ischemic stroke. Takeda sells the drug in Ja pan.<br />
OPSO TAKEDA (mor phine hy dro chlo ride) is an oral for mu la tion pre-pre pared in dos age units of 5mg<br />
and 10mg. It is in di cated for mod er ate to se vere pain in can cer, and was launched in Ja pan in 2003.<br />
OXYCONTIN TAKEDA (oxycodone) is a re tard-film coated tab let for mu la tion used for mod er ate to se -<br />
vere pain in var i ous types of can cer. It was launched in Ja pan in 2003.<br />
PREPENON TAKEDA (in ject able mor phine hy dro chlo ride) was launched in Ja pan in 2001, through a<br />
part ner ship with Terumo (Ja pan). It is in di cated for the re lief of pain in can cer pa tients. Takeda is re spon -<br />
si ble for sales and Terumo for de vel op ment and pro duc tion. Prepenon is sold in pre-filled sy ringes, in -<br />
creas ing con ve nience for pa tients treat ing themselves at home.<br />
PROVIGIL (modafinil), a non-am phet amine psychostimulant for narcolepsy and id io pathic<br />
hypersomnia. It was first launched in France in 1994 for the treat ment of narcolepsy and id io pathic<br />
hypersomnia, and has sub se quently been launched in most mar kets world wide, in clud ing the USA, Eu -<br />
rope, Can ada and Aus tra lia, and is await ing ap proval in Ja pan for this in di ca tion. In Au gust 2006 the US<br />
FDA is sued a non-ap prov able let ter for Cephalon’s s NDA for the use of modafinil in the treat ment of at -<br />
© 2009 <strong>IMS</strong> Health In cor po rated or its af fil i ates Page 45