An innovative Chinese Alzheimer’s drug that hit the domestic market last week, will go through clinical trials on 2,000 patients overseas in 2020.
The orally administered drug GV-971 will be tested in 200 clinical centers in North America, the European Union, Eastern Europe, Asia Pacific and other places, according to Green Valley Pharmaceutical Co., Ltd, one of the drug’s co-developers.
The company says it plans to complete the global clinical trials in 2024 and submit the New Drug Application to the U.S. Food and Drug Administration and European Medicines Agency in 2025.
GV-971 was jointly developed by the Shanghai Institute of Materia Medica under the Chinese Academy of Sciences (CAS), Ocean University of China and Green Valley, after a 22-year study.
The results of the mechanism of action study were published in the international journal Cell Research in September 2019, saying that the drug, extracted from brown algae, works by modifying gut bacteria to ultimately reduce brain inflammation in mice that were genetically engineered to have the disease.
It was approved to market last November by China’s National Medical Products Administration, which said the GV-971 “can improve cognition in patients with mild to moderate Alzheimer’s disease (AD).”
According to researchers, apart from animal experiments, more than 1,100 Chinese AD patients participated in clinical trials before the drug hit the market. In the last test, a total of 818 participants from 34 leading hospitals in China took 450 mg GV-971 orally twice a day for a treatment period of nine months, which proved safe and effective in improving cognition.
“Because of its effectiveness on Chinese patients, we expect this drug to benefit more people in the rest of the world,” said Lyu Songtao, chairman of the Shanghai-based pharmaceutical company.