Bispecific designs patent application
09 August 2022
Fusion Antibodies plc (AIM: FAB), specialists in pre-clinical antibody
												discovery, engineering and supply for both therapeutic drug and
												diagnostic applications, announces that it has submitted a patent
												application in respect of the Company’s bispecific designs for antigen
												display. 
The Company uses antigens to generate and screen for specific antibodies
												during the Antibody Discovery process. Fusion’s new designs for antigens
												consist of two parts; the antigen part and a “reporter” part, referred
												to as a “bispecific”. The Company believes that the use of a reporter
												part, which can be any number of useful tags for various antibody
												screening assays, will increase the success rate in identifying highly
												potent antibodies from Fusion’s range of Antibody Discovery
												technologies.
Simon Douglas, Chairman of Fusion, commented: “Our dedicated team of scientists continues to work on next generation antibody discovery, and we see significant opportunities in this field. We look forward to contributing to the growing body of research concerning the scope of antibody production and design, while also growing our patent portfolio."
Enquiries:
| Fusion Antibodies plc | www.fusionantibodies.com | |
| Simon Douglas, Chairman James Fair, Chief Financial Officer  | 
														Via Walbrook PR | |
| Allenby Capital Limited | Tel: +44 (0)20 3328 5656 | |
| James Reeve/Vivek Bhardwaj (Corporate
															Finance) Tony Quirke (Sales and Corporate Broking)  | 
														||
| Walbrook PR | Tel: +44 (0)20 7933 8780 fusion@walbrookpr.com | |
| Anna Dunphy | Mob: +44 (0)7876 741 001 | |
| Paul McManus | Mob: +44 (0)7980 541 893 | |
About Fusion Antibodies plc
Fusion is a Belfast-based Collaborative Research Organisation ("CRO")
												company, listed on AIM, providing a range of antibody engineering
												services for the development of antibodies for both therapeutic drug and
												diagnostic applications.
Fusion provides a broad range of services in antibody generation,
												development, characterisation, optimisation, and small-scale production.
												These services include antigen expression, purification and sequencing,
												antibody humanisation using Fusion's proprietary CDRxTM platform and
												cell line development, producing antibody generating stable cell lines
												optimised for use downstream by the customer to produce material for
												clinical trials. Since 2012, the Company has successfully sequenced and
												expressed over 250 antibodies and successfully completed over 200
												humanisation projects for its international customer base, which has
												included eight of the top 10 global pharmaceutical companies by
												revenue.
At every stage, our client's vision is central to how we work in
												combining the latest technological advances with cutting edge science.
												In this work our world-class humanization and antibody optimization
												platforms harness the power of natural somatic hypermutation (SHM) to
												ensure the best molecule goes to the clinic. Fusion Antibodies' growth
												strategy is based on enabling Pharma and Biotech companies get to the
												clinic more effectively, using molecules with optimized therapeutic
												profile and enhanced potential for successful development and approval
												and, ultimately, on speeding up the drug discovery and development
												process. Fusion's use of SHM to create a fully human antibody library to
												capture the human antibody repertoire will address a continuing market
												need in antibody discovery,
Fusion Antibodies' emphasis on antibody therapeutics is based on the size
												and growth rate in the sector, with the market valued at $135.4 billion
												in 2018 and forecast to surpass $300 billion by 2025, a CAGR of 14.26%.
												As of May 2021, there were 100 approved antibody therapies on the market
												and more than 570 antibody therapies in clinical development.
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