Biosyngen, an immune-oncology company with technology targeting the unmet medical needs in solid tumour and lymphoma treatment, announced the official opening of its latest Good Manufacturing Practice (GMP) facility in Singapore. The GMP will support cell manufacturing for immunotherapies in Singapore and across the World for the cell and gene therapy (CGT) industry in the next three to five years for gobally.
The opening was officiated by Mr Alvin Tan, Minister of State for Trade and Industry, and executives from Biosyngen including Ms Joan Zhang, Chairman of Biosyngen, Dr Benjamin Seet, Board Member of Biosyngen, Dr Michelle Chen, Chief Operation Officer and Prof. Jean Paul Thiery, Chief Scientist of Biosyngen. The opening was also witnessed by distinguished guests from Ministry of Health, Enterprise Singapore, Economic Development Board, Singapore Exchange, The Agency for Science, Technology and Research and National Cancer Centre Singapore.
The new facility is the first and the largest privately owned fully automatic and enclosed integrated GMP cell manufacturing facility and R&D base in Singapore so far, compliant with the latest FDA (U.S. Food and Drug Administration) recommendation, enabling Biosyngen to run automatic and closed-system production – the preferred best practice in the CGT industry. Designed with containment within each production suite, this facility can support multiple clinical trials in parallel.
"In the Singapore 2030 plan, advanced manufacturing and BioPharm is a key component. The opening of Biosyngen's GMP Facility contributes directly to the 2030 plan. It is the first and so far the largest privately owned GMP manufacturing facility in Singapore. Government will continue to support the growth of this sector," said Mr Alvin Tan, Minister of State for the Ministry of Trade & Industry.
"Through years of effort by the Biosyngen team, our first-in-class products targeting nasopharyngenl carcinoma and EBV+ lymphoma were granted IND by US FDA and CN NMPA; and recently granted orphan drug designation status as well. Just this month, we submitted IND applications for two other indications, lung cancer and liver cancer, to both FDA and NMPA. From our humble beginning in Singapore, renting a facility from Temasek Lifesciences Lab, we're embarking on this new GMP Facility for patients worldwide. The urgency in increasing speed in clinical trials for patients and building capacity for global needs. Biosyngen is determined to become a leader in the CGT industry." Dr. Michelle Chen, COO Biosyngen.
"We are a company dedicated to giving cancer patients a new lease of life by developing first-in-class immunotherapies. We aim to achieve this through our Research & Development (R&D) and collaborations with key stakeholders in hospitals, the wider industry and governments. Having two sites, one in Singapore and China, is a key global strategy for Biosyngen to advance the company's product pipeline quicker, and drive R&D and GMP manufacturing from both site," said Isaac Chow, CBO Biosyngens.
"Our facility in Singapore enables R&D in drug discovery and process development, and will also be able to accommodate more advanced processes or products that will be introduced in the future," added Dr Cecilia Zhang, CSO Biosyngen.
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