NMPA approves Hansizhuang, its first monoclonal antibody
Drug Approval

NMPA approves Hansizhuang, its first monoclonal antibody

It also empowers domestic precision immunotherapy for tumours and promotes the high-quality development of China's biopharmaceutical industry

  • By IPP Bureau | March 27, 2022

Shanghai Henlius Biotech announced that its first self-developed innovative PD-1 inhibitor Hansizhuang (generic name: serplulimab injection) has been approved by the National Medical Products Administration (NMPA) for the treatment of adult patients with advanced unresectable or metastatic MSI-H (Microsatellite Instability-High) solid tumours that have failed to respond to previous standard treatments, providing an alternative treatment option for patients. Furthermore, it also empowers domestic precision immunotherapy for tumours and promotes the high-quality development of China's biopharmaceutical industry.

Zhang Wenjie, Chairman, Executive Director, and CEO of Henlius, said, "I'm very glad to see the first indication of Hansizhuang was approved in China. As one of the pioneering PD-1 inhibitors for the 'pan-cancer' treatment of MSI-H solid tumours in China, Hansizhuang would give full play to its advantages in clinical practice to enable patients to live longer with more comfortable lives and accelerate the development of tumour immunotherapy. In addition, Hansizhuang is the fifth product launched by Henlius as well as a significant milestone in the company's evolution toward Biopharma, which will actively drive Henlius to move forward, and inspire more innovative achievements centered on patient needs."

Professor Qin Shukui, one of the co-leading principal investigators of the pivotal phase II clinical study of Hansizhuang on MSI-H solid tumours, from the Tumor Center of Nanjing Jinling Hospital, said, "PD-1 inhibitor is one of the immune checkpoint inhibitors that has been explored in some diseases, which makes breakthroughs in many tumour treatments. The clinical research data of Hansizhuang for MSI-H solid tumours is outstanding and will actively improve the clinical efficacy and provide a new mindset and alternative option for the precision treatment for tumours in China."

The results of this clinical study were first presented in oral at the 24th annual meeting of Chinese Society of Clinical Oncology (CSCO).

Upcoming E-conference

Other Related stories

Startup

Digitization