
Date and time:13:30 - 14:30, Monday, May 15, 2006
Location:10th Floor Conference Room, DAIICHI SANKYO Head Offices
A1. It is fine to understand that this to be temporary. In fiscal 2006, two American companies have posted sales from the portion for 15 months, that is, as a result of modifications to the fiscal term, and Zepharma newly joined the group, therefore the tradition expectations are changing. There is a need to review sales for fiscal 2007, including these modification contributors.
A2. The strengths of Daiichi Asubio Pharma are in biotechnology-based drugs and peptide research, and we wish to work on drug discovery by taking advantage of these features. Concerning company structure, we wish not to stay independent going forward, instead we will devise development fields and drug discovery fields within our interim-term management plan that would generate the most synergy for Daiichi Sankyo Group.
A3.We have no such plan.
A4. The status is as announced by AnGes MG. The status of development concerning peripheral arteriosclerosis is planned for announcement at the annual meeting of the American Society for Vascular Surgery to be held in Philadelphia, USA, in June. Concerning ischemic heart disease, there are issues with the catheter, however, no particular adverse effect was confirmed.
A5. Last year we obtained the approval on the combination drug. Drug price and such vary by country, however, we plan to take this to market from this summer to autumn in France and Italy. In addition, we also plan to sell Olmesartan as a single agent in China.
A6. The format for prescriptions changed starting this April, and since it has been only a month, we cannot make any statements. Also, the national policy is to actively promote the use of generic drugs, and we cannot fight national policy. Prescription drug companies will supply a level and quality of information that generic drug companies cannot perform. For example, we supply information such as mega-studies on Mevalotin, which is something that generic drug companies can in no way do.
A7. Daiichi Pharmaceutical had planned a joint sales, however, the scheme changed during the integration. We also believe an agreement was reached that has the least anti-synergy to Daiichi Sankyo.
A8. We wish to take the sales to 100.0 billion yen in the mid to long term. In addition, we newly entered the market on skin care and health food, and expect about 30% of the sales from there.
A9. We plan to limit co-promotions to 2 products until March 2007. Relatedly, each company has already performed training on products of the other company.
A10.We plan to have a 2,500-person structure for MR. The organization design is mostly completed.
A11. In the US, 70~80% of drugs become generic drugs within a year after the patents expire. Authorized generics is perhaps possible as a countermeasure to generic drugs, however, the situation in the US is that evidence like mega-studies are utilized not for Mevalotin but for Pravastatin drug overall.
A12.We have planned for approximately 9,000. We are currently planning the staff count needed for the organization.