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Home Manufacturing

Imvaq Therapeutics Signs a Service and Commercial Product License to Use ProBioGen’s AGE1.CR Vaccine Manufacturing Platform

Content Team by Content Team
8th January 2022
in Manufacturing, News
Johnson & Johnson Prepares to Resume Phase 3 ENSEMBLE Trial of its Janssen COVID-19 Vaccine Candidate in the U.S.

Note* - All images used are for editorial and illustrative purposes only and may not originate from the original news provider or associated company.

ProBioGen AG is delighted to announce the execution of a service and commercial product license agreement with Imvaq Therapeutics, a biotech company developing innovative cancer immunotherapies. Under this agreement, ProBioGen develops a scalable process and granted Imvaq® a license to use ProBioGen’s AGE1.CR.pIX cell line for the manufacturing of a MVA-based cancer immunotherapy candidate.

ProBioGen’s duck suspension cell line AGE1.CR.pIX is designed to support industrial, GMP-compliant production of a wide variety of vaccine strains and viral vectors in different bioreactor formats in chemically-defined media. The cell line has been exhaustively tested against adventitious agents and vectors produced on AGE1.CR.pIX have been used in clinical trials.

Dr. John Choi, CEO of Imvaq said: “After an initial demonstration study, the AGE1.CR.pIX platform convinced us to engage ProBioGen for process development to initiate a rapid and scalable manufacturing process for our uniquely engineered cancer immunotherapy and to negotiate a commercial license of this outstanding platform.”

Dr. Volker Sandig, Chief Scientific Officer at ProBioGen stated: “Yields and purity are important determinants for successful implementation of vaccines or virotherapeutics. The AGE1.CR.pIX cell line was shown to be highly permissive for innovatively designed vectors and we are pleased to complement Imvaq’s novel cancer immunotherapy strategy with our manufacturing approach.”

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