PerkinElmer’s Horizon Discovery CHOSOURCE Cell Line Supports Trinomab Biotech’s Development of the World-First, Tetanus Toxin mAb Drug for Clinical Trials

04 Feb 2021 | Press release

WALTHAM, Mass. – February, 4, 2021 – PerkinElmer, a global leader committed to innovating for a healthier world, today announced that its Horizon Discovery CHOSOURCE™ CHO-K1GS knockout cell line licensed by Trinomab Biotech. Co., Ltd. (www.trinomab.com), of Guangzhou, China was used to help produce and bring to clinical trial the world’s first, fully native human monoclonal neutralizing antibody (mAb) drug candidate to fight tetanus toxin.

Officially approved by the Australian Therapeutic Goods Administration (TGA) and Human Research Ethics Committee (HREC), the phase I clinical trial in Australia is expected to be completed in August 2021. Leveraging Horizon’s CHOSOURCE cell line, which includes a gene-edited Glutamine Synthetase (“GS”) knockout Chinese Hamster Ovary (CHO) K1 cell line and well-established GS expression system, Trinomab was able to get its drug candidate from DNA sequence to clinical manufacturing more quickly and easily.

Trinomab Biotech explained: “Since implementing the CHOSOURCE CHO-K1 knockout cell line in our drug development workflow in March 2019, we have been able to hit the ground running and develop this mAb drug candidate against different diseases including the first in-human mAb in phase I trial in Australia against tetanus toxin. These efforts have shown how easy and effective the Horizon cell line was to implement and adapt to our processes. We are pleased with the results and continue to build our drug pipeline using the CHOSOURCE CHO-K1 cell line”.

“We are delighted that the CHOSOURCE cell line has been part of Trinomab’s pioneering efforts to combat disease and are pleased to be working with other organizations in China and around the globe to move drug science and new therapeutic candidates forward,” commented Jesús Zurdo, Global Head Bioproduction in PerkinElmer’s Horizon business.

The CHOSOURCE platform, designed for pharmaceutical, biotechnology and biosimilar companies of all sizes, is recognized by the industry and regulators as optimized for high yield bioproduction and is licensed by more than 80 organizations globally. More than nine biotherapeutics expressed in these cell lines, including Trinomab’s, have progressed to investigational new drug (IND) filings.

For further information on PerkinElmer’s Horizon Discovery CHOSOURCE technology please visit: https://horizondiscovery.com/en/chosource.

About PerkinElmer

PerkinElmer enables scientists, researchers, and clinicians to address their most critical challenges across science and healthcare. With a mission focused on innovating for a healthier world, we deliver unique solutions to serve the diagnostics, life sciences, food, and applied markets. We strategically partner with customers to enable earlier and more accurate insights supported by deep market knowledge and technical expertise. Our dedicated team of about 14,000 employees worldwide is passionate about helping customers work to create healthier families, improve the quality of life, and sustain the wellbeing and longevity of people globally. The Company reported revenue of approximately $3.8 billion in 2020, serves customers in 190 countries, and is a component of the S&P 500 index. Additional information is available through 1-877-PKI-NYSE, or at www.perkinelmer.com.

About Trinomab

Trinomab is a biopharmaceutical start-up focused on the research and development of new, fully native human antibody drugs to fight infectious, autoimmune, and other diseases as well as malignant tumors. The core technology of the company is a fourth-generation antibody HitmAb®, a proprietary technology platform. Additional information is available at www.trinomab.com.

Media Contact:

Jennifer McNeil

jennifer.mcneil@perkinelmer.com

+1 508.380.2902