Akron Biotech signs agreement with Synairgen

Published: 19-Oct-2020

Akron provides cGMP solutions to support the development and commercialisation of advanced therapies

Akron Biotechnology has signed an agreement with Synairgen for the provision of SNG001, Synairgen’s inhaled interferon beta (IFN-beta) therapeutic candidate for the treatment of COVID-19 patients.

Synairgen reported positive results from its Phase II trial of SNG001 in 101 hospitalised COVID-19 patients in July 2020, indicating that its inhaled IFN-beta could provide a treatment option for COVID-19. Furthermore, the safety, biomarker, and efficacy data for SNG001 provided from the interim analysis of Synairgen’s Phase II COPD trial in September 2020 was supportive of the ongoing development of SNG001 in COVID-19 patients.

Akron will support the future clinical and commercial development of SNG001 through the provision of its IFN-beta in Synairgen’s formulation. “Akron’s expertise in recombinant protein manufacturing and large-scale production capacity add significant value to our further development and commercialisation of SNG001,” commented Synairgen CEO Richard Marsden. “The ability to rapidly scale the production of SNG001 will allow Synairgen to meet expected clinical and commercial demand for the drug, ensuring that patients have access to this promising treatment.”

“The agreement with Synairgen reflects our ongoing commitment to meet the growing demand for validated, cGMP-compliant solutions to advance novel therapies,” said Claudia Zylberberg, PhD, Founder and CEO of Akron Biotech. “We are excited to support Synairgen in its quest to further this exciting treatment for COVID-19, bringing a promising new therapy to patients with few viable options.”

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