The Preferred Biotech Resource in Asia-Pacific
Vol 19, No 07, July 2015
Biotech in China
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INSIDE INDUSTRY
DSM and Tunitas Therapeutics to develop lead allergy therapeutic

DSM Pharmaceutical Products, a custom manufacturing and technology business of Royal DSM, has entered an agreement with Tunitas Therapeutics of San Francisco, USA, an early stage drug development company dedicated to the discovery and development of a broad platform of therapeutic proteins for allergies.

The contract covers the initiation of process development activities by DSM for Tunitas' lead Fc-fusion protein for the treatment of asthma and other allergic diseases. The intended manufacturing site is DSM Biologics' Brisbane facility.

"We are delighted to be working with DSM Biologics for the production of Tunitas' first clinical candidate." said Nolan Sigal, President and CEO of Tunitas Therapeutics. "DSM has an outstanding and well-earned reputation for the production of biologics of the highest quality. Furthermore, the opening of the DSM's state-of-the-art facility in Brisbane fits nicely with our strategy to begin development activities in Australia."

Manja Bouman, President of DSM Biologics, commented "It is an honor to support the development of Tunitas' promising drug candidate from our facilities. We are impressed with the potential of this product and the health benefit to treat the millions of patients whose asthma is poorly-controlled on their current therapeutic regimens."

DSM Biologics, a business unit of DSM Pharmaceutical Products, focuses on optimizing mammalian-based biopharmaceutical manufacturing through its unique set of technologies and expertise. In addition to an R&D and manufacturing site in Groningen, The Netherlands, DSM has opened operations in Brisbane, Australia, with the support of the Governments of Queensland and the Commonwealth. The Brisbane facility is DSM's blueprint for its 'biologics plant of the future' for the production of biopharmaceuticals. DSM's proprietary technologies drive down cost, processing times and capital requirements to meet market demand for developing affordable lifesaving medications.

Source: B3C Newswire

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