
Le Meridien Vaccine is a large-scale private vaccine group with a full industry chain in China. Its business covers the entire industry value chain from R&D to manufacturing to commercialization. It obtained batches of about 60 million doses in 2020, achieving sales of vaccine products to 31 provinces, autonomous regions and municipalities directly under the Central Government of China. Le Meridien has five vaccine companies that have proven human vaccine platform technology, which greatly guarantees the speed and flexibility of the company's development. Currently, the company has 8 commercial vaccines for 6 disease fields and 23 innovative vaccines under development for 13 disease fields. The products in production and development cover all of the world's top ten vaccine products (based on global sales in 2020). Through ten years of development, the company has developed an inclusive and pioneering business model and corporate culture, through which it has been able to continuously expand and optimize its existing business. Currently, four licensed vaccine manufacturers are wholly owned, namely Le Meridien, Emmy Conhuai, Emmy Weixin, and Rongan Biotech. It owns 3 research institutes, of which the R&D center, Le Meridien Explorer, which was built in 2018, focuses on providing technical support for early and cutting-edge research by R&D departments in various factories. Le Meridien acquired Zhuhai Lifanda Biotechnology Co., Ltd. in 2021. The company is one of only 3 domestic companies to obtain approval for clinical trials of the mRNA COVID-19 vaccine, and has an independent mRNA production and drug delivery technology platform. Le Meridien Vaccine Group has always adhered to the mission of “making vaccines of conscience and living a healthy world” and strictly controls the quality of vaccines. The company is equipped with a professional and dedicated sales team composed of more than 100 members with an average of more than 10 years of experience in drug or vaccine sales. The core business leadership team has an average of 12 years of vaccine commercialization experience for multinational pharmaceutical companies, and has excellent results in marketing major international vaccines (including the world's first HPV, IPV, and dTAP-IPV-Hib). The products currently on sale mainly include recombinant hepatitis B vaccine (Hanson's yeast), freeze-dried human rabies vaccine (Vero cells), hepatitis A inactivated vaccine (human diploid cells), live attenuated mumps vaccine, bivalent renal syndrome hemorrhagic fever inactivated vaccine (Vero cells), and ACYW135 group meningococcal polysaccharide vaccine (MPSV4).
相关临床试验
13
9 进行中
药物批准
0
批准总数
监管机构
0
监管机构数
成立时间
2011
进行中(未招募)
6
46.1%
已完成
1
7.7%
尚未招募
3
23.1%
招募中
3
23.1%
暂无批准数据
- AIM Vaccine has submitted its novel mRNA RSV vaccine for FDA clinical trials, demonstrating superior humoral and cellular immunity compared to existing marketed products in preclinical studies. - The company's mRNA RSV vaccine development comes at a crucial time, with the global RSV vaccine market projected to reach USD 16.7 billion by 2030 and no approved vaccines currently available in China. - Multiple financial institutions, including FOSUN INTERNATIONAL SECURITIES and SDICSI, have issued "Buy" ratings for AIM Vaccine, citing strong product pipeline and international growth potential.
- AIM Vaccine Co., Ltd. has pre-applied for marketing approval of its serum-free rabies vaccine, which showed excellent safety and immunogenicity in Phase III trials. - The innovative vaccine is designed to reduce allergic reactions by eliminating animal serum, potentially becoming the first of its kind available worldwide. - With infrastructure ready for large-scale production, AIM Vaccine aims to improve global vaccine quality and safety in rabies prevention.
- AIM Vaccine Co., Ltd. has submitted its 13-valent pneumonia conjugate vaccine for drug marketing registration to China's National Medical Products Administration. - Phase III clinical trials demonstrated the vaccine's good immunogenicity and safety, successfully meeting pre-defined clinical objectives for the target population. - The 13-valent pneumonia conjugate vaccine is designed for infants and children aged 6 weeks to 5 years to prevent invasive diseases caused by 13 pneumonia serotypes. - With a significant market opportunity in China, the vaccine aims to address the underserved demand for pneumonia prevention, potentially enhancing the company's performance.