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1)
Pipeline:
We currently have four projects under development –
three of them will be in the clinical stage in 2007.
We also have access to a wide variety of in-licensing
opportunities throughout Japan and abroad.
2) Experience and
expertise:
Our top management and board of directors encompass
more than 20 years of experience on average in the Japanese
and international pharmaceutical industries, including
firms such as Eisai, Santen, Astellas, Pfizer, Kyowa
Hakko, Roche (Chugai) and Novartis. We have been involved
in the registration of more than 10 drugs, including
teprenone (Selbex; Eisai), rabeprozole sodium (Pariet;
Eisai), valsartan (Diovan; Novartis), chimeric anti-TNFa
antibody (Remicade; Centocor/Tanabe), oseltamivir (Tamiflu;
Roche) and sildenafil citrate (Viagra; Pfizer). Our
knowledge and experience span not only preclinical (GLP)
and clinical (GCP) drug development, regulatory affairs,
QA/QC, manufacturing (GMP), and the management of external
resources such as CROs, but also licensing and business
development, and intellectual properties.
3) Network:
Using our extensive network that spans the pharmaceutical
industry, academia and the investment community, we
can quickly identify in-licensing opportunities; track
overall drug discovery, drug development, regulatory,
and sales & marketing trends in the larger industry;
and target potential partners for future out-licensing
of our products. |