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Ascentage Approved to Start China Trial of Apoptosis Drug

publication date: Jul 18, 2017
Ascentage Pharma was granted Investigational New Drug (IND) approval by the CFDA for APG-1252, a novel Bcl-2/Bcl-XL inhibitor. APG-1252, one of three programmed cell death candidates in Ascentage's development pipeline, started a Phase I trial in the US earlier this year. The trial will enroll patients with small cell lung cancer. Ascentage is headquartered in Hong Kong, but operates an R&D facility in Shanghai and a lab/manufacturing facility in Taizhou's China Medical City. The company raised $72 million in a B round in late 2016. More details....

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