Chinese companies are riding high on antibody drug conjugate partnerships and collaborations.
“Our collaboration with SystImmune allows us to strengthen our leadership in oncology and is consistent with our strategy to diversify beyond immuno-oncology to transform patient care,” said Samit Hirawat, MD, Executive Vice President, Chief Medical Officer, Drug Development at Bristol Myers Squibb.
Currently only 13 ADCs are approved by the U.S. and Europe in the market but the promising pipeline of more than 250 candidates is under clinical evaluation, signaling a targeted shift in the cancer treatment. In the Asia Pacific region, the development of ADCs is accelerating through new deal-making and clinical trials. China is running behind this opportunity with high-end partnerships and collaborations with global biopharma companies. This strategy adopted by Chinese companies are advancing the clinical evaluation activities for ADCs in APAC region.
China not only leads in Phase 1 trials but also ranking at second place in the phase 2 development globally. From 2022 to 2024, it has witnessed a surge in ADC licensing deals attracting global pharmaceutical companies. These partnerships are showcasing the country’s focus on advancing biotech innovation. Biotech companies such as Kelun Biotech, Duality Biologics, and Hansoh Pharma are the key players in the ADC development, undergoing landmark licensing deals with major pharma companies such as GSK, BioNTech & others.
Going forward China is witnessing a wave of deal making with U.S. European, and Japanese pharma companies. This deal value in between 2022-2024 was valued at USD 1,988 million, showcasing China’s capabilities in drug discovery & development.
“We are very pleased that the NDA application for the fourth indication of our core product, sac-TMT, has been accepted by the CDE of NMPA, which is another breakthrough for the breast cancer treatment field”, said by Dr. Michael Ge, CEO of Kelun-Biotech.
These partnership highlights that China is becoming the global research and development center for antibody drug conjugates. The country is accounting for nearly 60% of all newly registered global ADC trials in 2023 as compared to less than 20% in 2020. Factors such as robust clinical trial infrastructure, strong R&D capabilities, high operational efficiency are the key parameters advancing the clinical development in China.