Global
CDMO utilizes Seattle facility’s mammalian biologics expertise to
support late-stage clinical trials for leading international biopharma
organization
Seattle, Dec 14 (Bernama-GLOBE NEWSWIRE) -- AGC Biologics, a leading global Biopharmaceutical Contract Development and Manufacturing Organization (CDMO), today announced a new partnership with I-MAB Biopharma (Nasdaq: IMAB). The I-MAB treatment being developed is approaching late-phase clinical trials and AGC Biologics will manufacture the materials at its site in Seattle, while also supporting the launch readiness of I-MAB’s product.
AGC Biologics operates multiple mammalian cGMP manufacturing lines and a variety of scales at its Seattle cell culture facility. The site is designed for capacity and technological flexibility, and has an extensive variety of single-use and stainless steel systems that meet the latest guidelines required for cGMP compliance. The Seattle site also has a long history of successful inspections by the FDA and the site is approved for commercial production. All of these features and capabilities combined make the AGC Biologics Seattle facility an ideal location to support I-MAB’s goals and bring this treatment through its next clinical phase.
“We look forward to partnering with a true pioneer in innovative clinical research and development, and working together to help bring I-MAB's product through the final clinical stages and to commercialization,” said Jean-Baptiste Agnus, Chief Business Officer of AGC Biologics. “Our team in Seattle is an ideal customer-focused group of scientists to help I-MAB in its promising journey for this treatment.”
AGC Biologics’ Seattle facility has capabilities for developing a wide range of mammalian and microbial programs, and has delivered several approved commercial products.
To learn more about the biologics capabilities AGC Biologics offers across its network of seven global facilities visit www.agcbio.com/capabilities.
About AGC Biologics
AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan and we currently employ more than 2,000 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit www.agcbio.com.
Nick McDonald
AGC Biologics
(425) 419-3555
nmcdonald@agc.com
SOURCE : AGC Biologics
Seattle, Dec 14 (Bernama-GLOBE NEWSWIRE) -- AGC Biologics, a leading global Biopharmaceutical Contract Development and Manufacturing Organization (CDMO), today announced a new partnership with I-MAB Biopharma (Nasdaq: IMAB). The I-MAB treatment being developed is approaching late-phase clinical trials and AGC Biologics will manufacture the materials at its site in Seattle, while also supporting the launch readiness of I-MAB’s product.
AGC Biologics operates multiple mammalian cGMP manufacturing lines and a variety of scales at its Seattle cell culture facility. The site is designed for capacity and technological flexibility, and has an extensive variety of single-use and stainless steel systems that meet the latest guidelines required for cGMP compliance. The Seattle site also has a long history of successful inspections by the FDA and the site is approved for commercial production. All of these features and capabilities combined make the AGC Biologics Seattle facility an ideal location to support I-MAB’s goals and bring this treatment through its next clinical phase.
“We look forward to partnering with a true pioneer in innovative clinical research and development, and working together to help bring I-MAB's product through the final clinical stages and to commercialization,” said Jean-Baptiste Agnus, Chief Business Officer of AGC Biologics. “Our team in Seattle is an ideal customer-focused group of scientists to help I-MAB in its promising journey for this treatment.”
AGC Biologics’ Seattle facility has capabilities for developing a wide range of mammalian and microbial programs, and has delivered several approved commercial products.
To learn more about the biologics capabilities AGC Biologics offers across its network of seven global facilities visit www.agcbio.com/capabilities.
About AGC Biologics
AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan and we currently employ more than 2,000 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit www.agcbio.com.
Nick McDonald
AGC Biologics
(425) 419-3555
nmcdonald@agc.com
SOURCE : AGC Biologics
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