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ProBioGen and Marea Therapeutics Accelerate MAR002 Antibody

Complete a sprint project to deliver clinical material for the investigational anti-growth hormone receptor (GHR) antibody.

ProBioGen and Marea Therapeutics Inc. have successfully completed a sprint project to deliver clinical material for MAR002, Marea’s investigational anti-growth hormone receptor (GHR) antibody for the treatment of acromegaly. The partnership encompassed cell line development, process development, formulation development, and GMP manufacturing services.

The collaboration leveraged ProBioGen’s CHO.RiGHT cell line development platform, including its proprietary DirectedLuck transposase technology, to generate superior, high-yielding clone pools for early material production for IND-enabling toxicology studies. The stable platform also enabled the development of a robust, scalable manufacturing process, including integrated, seamless drug product (DP) manufacturing at Marea’s DP partner, contributing to the successful development of MAR002.

“We are pleased to have successfully completed this comprehensive project with Marea Therapeutics, delivering on our commitment to high quality and accelerated timelines,” said Dr. Alfred Merz, CEO of ProBioGen. “This collaboration exemplifies our customer-centric approach and our ability to support biotech companies with innovative and flexible solutions, enabling a sprint to IND to meet their challenging timelines. We look forward to seeing the continued progress of MAR002.”

Mark Joing, Chief Development Operations Officer of Marea, added: “MAR002 holds promise as a first-in-class treatment for acromegaly, a life-shortening disease often with serious complications. We appreciate ProBioGen’s support throughout the process and look forward to continuing our collaboration as we advance to the next stages.”

The partnership between ProBioGen and Marea Therapeutics has successfully laid the foundation for MAR002’s next development stages. With key CMC milestones achieved, Marea is well-positioned to advance the candidate further toward clinical and commercial readiness.

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