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Pharma  News  Story
Daiichi Sankyo seeks Japanese approval for Denosumab

Singapore, Aug 25, 2010: Japanese drug giant, Daiichi Sankyo, has filed for approval in Japan to manufacture and market AMG 162 (Denosumab), a gene recombinant drug for bone disorders stemming from bone metastases.

According to the company, Denosumab is the world’s first fully human monoclonal antibody to target RANK Ligand, an essential mediator of osteoclast formation. Daiichi Sankyo has been working on Denosumab since 2007, when it acquired the rights from Amgen to develop and market this antibody in Japan.

In addition, Daiichi Sankyo is conducting a phase III clinical trial for Denosumab to treat osteoporosis in Japan.

In Denosumab, Daiichi Sankyo aims to benefit patients, their families, and medical professionals by augmenting the few available therapeutic alternatives for treating disorders stemming from cancer-related bone metastases with a new and effective treatment option, noted the company release.

 

 

© BioSpectrum Bureau
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