China cancer monoclonal antibodies market is estimated to grow at a CAGR of 11.6% during the forecast period. An increasing launch of biosimilars has been witnessed in the country owing to the increasing focus on providing affordable cancer therapy in the country. For instance, in August 2020, China’s NMPA (National Medical Products Administration) approved a biosimilar version of Roche’s Herceptin (trastuzumab), Shanghai’s Henlius which is referred to as HLX02 to treat HER2-mutated cancers. As its reference product, this biosimilar is also used for the treatment of HER2-positive early breast cancer, metastatic gastric cancer, and metastatic breast cancer. This therapy was demonstrated to be very similar to Roche’s Herceptin regarding safety, efficacy, and quality in preclinical, Phase 1, and Phase 3 studies. It is expected that this therapy will benefit HER2-positive gastric cancer and breast cancer patients in China.
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Further, in June 2020, Innovent Biologics, Inc. declared the NMPA approval of BYVASDA (bevacizumab biosimilar). It is a recombinant humanized anti-VEGF monoclonal antibody drug for patients suffering from advanced metastatic colorectal cancer and non-small cell lung cancer in China. NMPA has approved Innovent’s second monoclonal antibody drug, followed by TYVYT (sintilimab injection), which is approved to treat patients suffering from Hodgkin's lymphoma in December 2018.
Scope of the China Cancer Monoclonal Antibodies Market
Market Coverage
Recent Strategic Initiatives in the China Cancer Monoclonal Antibodies Market
Key questions addressed by the report
o Recovery Timeline
o Deviation from the pre-COVID forecast
o Most affected country/segment
China Cancer Monoclonal Antibodies Market-Segmentation
By Type
By Application
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