Tokyo retreated in the week to January 12 (four trading days only because the last day was a national holiday in Japan). The Nikkei 225 was down 2.3%, to close at the 8,800 mark, while the Topix index fell 2.4%. The market opened higher but suffered a setback towards the weekend, reflecting profit-taking of export-oriented issues and a dearth of positive news. Investors continued to anticipate that forthcoming October-December 2008 quarterly earnings reports of Japanese companies - to be unveiled later this month - would likely involve some downward revisions to their full-year guidance due to the impact of the global economic downturn and the yen's strength. The pharmaceutical index dropped 4.7%, underperforming the market.
Takeda was off 2.8%, without responding to a report the previous week that it had commenced a Phase III clinical trial of ATL-962, a treatment for obesity-related diabetes or dyslipidemia. The drug, originated by the UK's Alizyme, has a mechanism of action for causing weight loss by reducing digestion or the absorption of fat from the diet. Takeda in-licensed the product in January 2004, acquiring exclusive rights to develop, manufacture and market it in Japan and is to pay milestones and royalties on future sales. Takeda's share performance was not aided either by the receipt of Ministry of Health, Labor and Welfare approval of an additional indication - concomitant therapy with biguanides - for Actos (pioglitazone), its insulin-sensitizer antidiabetes drug. Biguanides act primarily by reducing the amount of glucose produced by the liver. In the comparative study, Actos/biguanides concomitant therapy showed a statistically-significant difference from biguanides monotherapy on improving HbA1c without increasing the risk of hypoglycemia. Takeda expects that the concomitant therapy will offer an additional option for superior glycemic control.
Meiji Seika lost 2.9%, despite a media report that the company is set to release a new mid-term strategic plan for the fiscal years ending 2010 and 2012 targeting expansion of generic drug sales to 18.0 billion yen ($201.6 million) from the estimated 10.5 billion yen in the current fiscal year. The company also plans to expand sales of drugs in core therapeutic areas such as antibiotics and central nervous system treatments, expecting to receive an approval in Japan in the next fiscal year for ME1211, an oral carbapenem antibiotic for the treatment of respiratory tract infections, and Org3770, its antidepressant and antianxyolitic. The firm's detailing force is to be increased to 800 from 700 at present. Overseas business will be strengthened, with the planned introduction of the antibacterial drug Meiact (cefditoren pivoxil) in newly-developing countries.
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