AGC Biologics Adds Mammalian Production Capacity in Japan

September 21, 2018


New facility will include comprehensive mammalian process development and manufacturing capabilities

AGC Biologics, a global leader in clinical and commercial manufacturing of therapeutic proteins, announced today that as part of its ongoing program to expand its production capacities globally, it will establish a new state of the art process development and manufacturing facility at its CDMO facility in Chiba, Japan. The new facility, which is expected to be operational in the second half of 2019, will contain single-use bioreactors at the 500 and 2000L scale and will be ideally suited for the production of monoclonal antibodies (MAbs), fusion proteins and other
types of therapeutic proteins.

AGC Biologics currently provides mammalian protein process development and manufacturing services
from its facilities in Bothell, WA, Berkeley, CA and Copenhagen, Denmark as well as microbial process
development and manufacturing services from its facilities in Heidelberg, Germany, Copenhagen
Denmark, and Chiba Japan. The Company will leverage its extensive experience and expertise with
mammalian production systems to rapidly establish these services at its site in Japan.

“This is a key investment for AGC Biologics that will expand our capabilities and reinforce our leadership
position in the Japanese CDMO marketplace.” said Gustavo Mahler, PhD, Chief Executive Officer of AGC
Biologics. “Our new mammalian capabilities will represent a unique and convenient option for
companies in Asia seeking mammalian production services nearby and for US and European companies
seeking production in Asia.”


About AGC Biologics

AGC Biologics is a leading global Contract Development and Manufacturing Organization, with a strong
commitment to deliver the highest standard of service to our clients. AGC Biologics has an extensive
network of cGMP facilities in the US, Europe and Asia. We offer deep industry expertise, innovative
solutions and technologies, and customized services for the scale-up and cGMP manufacture of protein-based
therapeutics, from pre-clinical to commercial, for mammalian and microbial. We forge
exceptionally strong partnerships with our clients, and we never lose sight of our pledge to deliver
reliable and compliant drug substance supply, on time. For more information, visit