游艇会yth0008

    In early 2020, COVID-19 outbreaks spread around the world. Fosun Pharma actively investigated the progress of global vaccine research and development, sought international cooperation, and finally selected BioNTech, a leading German company in the field of mRNA vaccines, as a partner. On March 16, 2020, Fosun Pharma announced that it had signed a cooperation agreement with BioNTech for the authorization of clinical development and commercialization in mainland China and Hong Kong, Macao and Taiwan of the COVID-19 vaccines (including BNT162 vaccine candidate, etc.) developed by BioNTech through RNA technology platform.

    In April 2020, Fosun Pharma and the Institute of Laboratory Animals Science of CAMS & PUMC initiated the mouse challenge test and timely shared the test results with partners.

    In April and May 2020, BioNTech initiated a phase I/IIa clinical trial of BNT162b1/b2.

    On July 18, 2020, Fosun Pharma initiated a phase I clinical trial of BNT162b1 in China on the basis of partner data sharing.

    On July 27, 2020, BNT162b2 was finally selected for a global phase IIb/III clinical trial after multi-party evaluations.

    On November 9, the results of the first interim analysis showed that the efficacy of BNT162b2 was over 90% 7 days after completion of the vaccination procedure.

    On November 13, Fosun Pharma was approved to carry out a phase II bridging trial of BNT162b2 in China.

    On November 18, the final efficacy analysis of the global phase III clinical trial showed that BNT162b2 met all the primary efficacy endpoints of the study, with an effective rate of 95%.

    On November 24, Fosun Pharma held a phase II clinical trial initiation meeting in Taizhou, Jiangsu Province

    Fosun Pharma is making every effort to complete the clinical development, registration and marketing of the vaccine as soon as possible.

    SurVaxM is a peptide mimic immunotherapeutic vaccine (immunotherapy) that targets survivin, a cell-survival protein present inside or on the surface of 90% of glioblastoma and many other cancer cells. SurvAxM has a dual mechanism of action of stimulating T cell immunity, as well as antibody-mediated inhibition of the survivin pathway, which can control tumor growth and prevent or delay tumor recurrence.

    This project was introduced with an exclusive license from MimiVax, LLC (USA) in November 2019 for the clinical development, registration and marketing in mainland China, Hong Kong and Macao for the indications of glioblastoma and other tumors.