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Will upscale and manufacture Abera’s vaccine candidate against pneumococcus, Ab-01.12.
April 26, 2022
By: Charlie Sternberg
Associate Editor
Sweden-based NorthX Biologics, which focuses on process development and large-scale production of advanced biological drugs, has signed a collaboration agreement with Abera Bioscience for upscaling and GMP manufacturing of its vaccine candidate against pneumococcus, Ab-01.12. NorthX recently established an innovation hub to offer support to partners in achieving their long-term drug development goals. The company’s ability to handle new ways of working and experience with unique development demands was crucial in Abera’s decision-making. Abera Bioscience is a biotechnology company that develops vaccine candidates based on its proprietary vaccine platforms. The company’s main candidate, Ab-01.12, is a universal vaccine against pneumococcus given as a nasal spray. The company is preparing the vaccine candidate for clinical trials in humans. Eva-karin Gidlund, head of Alliance and Innovation at NorthX Biologics, said: “We at NorthX are proud of our collaboration with Abera. Abera is exactly the kind of player we have strived to work within our innovation hub – innovation-driven vaccine companies with a high level of research and knowledge of their own process, while they already have several exciting projects in the pipeline. “At NorthX Biologics, we pride ourselves on working with early stage companies and offer a partnership that is flexible, cost effective and driven by knowledge and experience,” Gidlund continued. “We grow with our customers, so we can’t wait to see where this journey with Abera takes us both.” Maria Alriksson, CEO of Abera Bioscience, said: “After evaluating a number of players, it seemed natural to choose NorthX Biologics. They have more than 30 years of experience in GMP and manufacturing and they best met the requirements for knowledge, flexibility and ability to deliver that Abera sought. Together with NorthX, Abera has prepared a plan for accelerated development of Ab-01.12 where they expect to be able to initiate toxicological studies during Q4 2022 and hope to be able to submit their dossier and application to begin clinical studies Phase 1 for Ab-01.12 during the first half of the year 2023.
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