Tiantan Biological subsidiary completes hemophilia drug trials
Chengdu Rong Sheng Pharmaceutical, a subsidiary of Beijing Tiantan Biological Products Corp., completed Phase III clinical trials for its recombinant human coagulation factor VII injection. The trials on patients under 12 with hemophilia A showed routine preventative treatment significantly reduced bleeding frequency and improved joint health and quality of life.
The clinical trial involved R&D investment of 797.4m yuan. Further applications to the National Medical Products Administration are required, with approval timeline uncertain.
This report was generated by FilingReader's AI system from regulatory filings and company disclosures. To request a correction, contact editorial@filingreader.com
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