Nikon and Lonza Form Collaboration for Cell and Gene Therapy Manufacturing in Japan
Japan has become an attractive location for the future of regenerative medicine since the induction of the Revised Pharmaceutical Affairs Act, which became effective in November 2014. The act states conditional product approval may be granted in Japan at the time when clinical safety and an indication of efficacy of a regenerative medicine product are demonstrated. For this reason Japan is expected to be a promising location for the expedited clinical application of cell and gene therapy products.
The use of somatic stem cells (hematopoietic stem cells and mesenchymal stem cells) has already gained traction in the United States and European biotechnology and pharmaceutical markets, with the use of induced pluripotent stem cells (iPSCs) following quickly behind.
In addition, virally modified gene therapy has demonstrated promising clinical results in multiple disease indications, including cancer. Using viral vectors, immune and stem cells can be genetically modified and reintroduced to the patient as a targeted therapy.
“This collaboration will contribute greatly to the growth of the global cell and gene therapy market,” said Andreas Weiler, Head of Emerging Technologies, Lonza Pharma&Biotech. “We are utilizing our expertise built over the last decade to work together with Nikon in bringing high-quality, innovative development and manufacturing to Japan. Because of its work in iPSC technology, we believe Nikon is an ideal partner for this collaboration in regenerative medicine.”
Nikon’s newly formed subsidiary, Nikon CeLL innovation Co., Ltd., will actively contribute to the early realization of Japan’s regenerative medicine market and over time will expand its business domain into adjacent technology areas. Furthermore, Nikon will also develop equipment and disposables needed to optimize the manufacture of high-quality cells, along with hardware and software from Japan to the international market.
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Topic world Gene therapy
Genetic diseases once considered untreatable are now at the center of innovative therapeutic approaches. Research and development of gene therapies in biotech and pharma aim to directly correct or replace defective or missing genes to combat disease at the molecular level. This revolutionary approach promises not only to treat symptoms, but to eliminate the cause of the disease itself.
Topic world Gene therapy
Genetic diseases once considered untreatable are now at the center of innovative therapeutic approaches. Research and development of gene therapies in biotech and pharma aim to directly correct or replace defective or missing genes to combat disease at the molecular level. This revolutionary approach promises not only to treat symptoms, but to eliminate the cause of the disease itself.