CanSinoBIO Launches Pneumococcal Vaccine: An Innovative Choice to Safeguard Children’s Health

Pneumonia is a form of acute respiratory infection, that is common in all age groups and can cause mild to life-threatening illness. It is also the single largest infectious cause of death in children worldwide.

According to the World Health Organization(WHO), pneumonia killed more than 808,000 children under the age of 5 in 2017, accounting for 15% of all deaths of children under 5 years. Notably, in China, non-invasive pneumococcal diseases(NIPD), result in approximately 550,000 cases annually, leading to around 6,000 deaths. Meanwhile, invasive pneumococcal diseases (IPD) are more severe, with over 7,200 cases of pneumococcal meningitis reported each year. The average treatment cost per case of IPD is approximately CNY 64,000, and the case-fatality rate exceeds 10%. Behind these stark numbers lie the heavy burdens on countless families and an urgent public health challenge.

Facing this challenge, CanSino Biologics Inc. (Stock Code: 688185.SH, 6185.HK, “CanSinoBIO” or “the Company”) has developed and launched its 13-valent pneumococcal conjugate vaccine, trade name “iPneucia®”, optimized for China’s local pneumococcal epidemiology, aiming to provide more precise and safer protection for Chinese children.

The main advantage of iPneucia® is its deep optimization based on China’s local epidemiological characteristics. Streptococcus pneumoniae is categorized into different serotypes based on polysaccharide structure and biochemical traits. However, not all serotypes pose the same threat; their pathogenicity and disease burden vary. Research indicates that serotypes 19F, 19A, 7F, and 3 are the four most burdensome for Chinese children, accounting for over 60% of cases. These serotypes are also characterized by high resistance and high risk of sequelae. Given these risks, iPneucia® is specifically designed to target these four high-risk serotypes, and clinical data show that the geometric mean concentration (GMC) of antibodies against these four serotypes in iPneucia® is significantly higher than in the control group. This targeted protection strategy greatly enhances the precision of prevention, reducing disease risks at the source.

The breakthrough of iPneucia® lies not only in its enhanced targeting serotypes protection effect, but also in its carrier technology. It pioneers a dual-carrier conjugate process that adopts CRM197 and tetanus toxoid(TT) as carrier proteins. This approach effectively avoids immune interference caused by excessive use of a single carrier and reduces the risk of immune suppression when co-administered with other vaccines, enhancing immunogenicity. Moreover, iPneucia® also adopts a more advanced carrier protein conjugation process, ensuring consistent polysaccharide antigen content across all serotypes, significantly reducing competition between components.

Notably, the process of using CRM197 carrier as carrier protein in iPneucia® does not require formaldehyde for detoxification, which improves vaccine safety. This is also supported by data from Menhycia, another CRM197-based vaccine developed by CanSinoBIO. Post-marketing surveillance data on adverse events following immunization (AEFI) for recipients of the Menhycia show a apparently decline in the incidence of AEFI, fever, and local induration..

In summary, iPneucia® offers precise protection by targeting key serotypes and innovative protein carrier technology, resulting in enhanced effectiveness while minimizing the risk of adverse reaction. It also utilize a mature production process that excludes phenol, further improving its safety profile. CanSinoBIO presents a superior option for preventing pneumococcal diseases in Chinese children.

As a leader in innovative vaccines, CanSinoBIO always dedicated to scientific research and exploration in vaccine development. The company strives to create innovative, high-quality, and affordable vaccines. CanSinoBIO is committed to tackling global health challenges and improving the health and well-being of children around the world.

CanSinoBIO, (688185.SH)(06185.HK), https://www.cansinobio.com

CanSinoBIO CSO Shares the Latest Results of the Company’s Globally Innovative Pneumococcal Vaccine

On April 20, the 2024 National Vaccines and Health Conference organized by the Chinese Preventive Medicine Association (CPMA) and the Chinese Center for Disease Control and Prevention (China CDC) took place in the Xiong’an New Area of Hebei Province. Dr. Tao Zhu, Chief Scientific Officer (CSO) of CanSino Biologics Inc. (CanSinoBIO), was invited to give a presentation at the conference.

Dr. Zhu introduced the latest progress and breakthrough made in the development of pneumococcal vaccines both in China and abroad, focusing on sharing the latest results from the clinical trials of the company’s globally innovative protein-based pneumococcal vaccine (PBPV). He said that the PBPV is unique in terms of its broader coverage, serotype-independent and simpler production process while triggering good immune memories, and is expected to further improve the protection against pneumococcal diseases. Positive results have been obtained from Phase I clinical trials of the PBPV.

The results of Phase Ia and Phase Ib clinical trials showed that PBPV has a good safety profile in adults aged over 18 years old (including the elderly over 50 years old). A single dose of vaccination was found induce significant binding antibody and functional bactericidal antibody responses against cross-family/clade of Streptococcus pneumoniae, which further demonstrated the broad spectrum and potential public health value of this vaccine candidate.

When talking about the platforms for the development of innovative vaccines as well as the development of multi-valent vaccines and conjugate vaccines, Dr. Zhu said that CanSinoBIO has built five such platforms and a highly competitive pipeline, including multiple vaccine candidates targeting 10-plus indications like meningitis, pneumonia, DPT, shingles, and tuberculosis.

Dr Zhu emphasized the company has developed a comprehensive strategy to combat pneumonia-related illness. He said that CanSinoBIO has laid a solid foundation for the subsequent development of those candidates and their launch in overseas markets with its unique vectors and animal component free media (ACFM). The company is committed to developing pneumococcal vaccines, especially higher-valency serotype vaccines to improve the effectiveness of vaccines.

In the future, CanSinoBIO will continue to drive the innovation and development of vaccines with a global vision by enhancing collaboration with international partners, and contribute more to public health around the world.

About PBPV

PBPV is a globally innovative pneumococcal vaccine candidate. Unlike the 23-valent pneumococcal polysaccharide vaccine (PPV23) and the 13-valent pneumococcal conjugate vaccine (PCV13), PBPV is not serotype-dependent. It mainly adopts antigens that are based on the pneumococcal surface protein A or PspA, which is a highly-conserved protein expressed by virtually all pneumococci. Compared with currently marketed PPV23 and PCV13, PBPV has broader coverage (at least 98% coverage of pneumococcal strains), which can effectively prevent serotype replacement. Meanwhile, this product has a simpler production process than polysaccharide vaccines and conjugate vaccines, facilitating scale-up and quality control.

About CanSinoBIO

Incorporated in 2009, CanSino Biologics Inc. (SSE: 688185, HKEX: 06185) commits to providing high-quality, innovative, and affordable vaccines for global public health security. It possesses five integrated platform technologies upon which the company has established a rich portfolio of a pipeline products preventing more than 10 diseases, including the Aisa’s first and only vaccine for Ebola virus disease Ad5-EBOV, the Recombinant Novel Coronavirus Vaccine (Adenovirus Type 5 Vector) Convidecia® approved in over 10 countries and granted EUL by the WHO, the Asia’s first Group ACYW135 Meningococcal Conjugate Vaccine (CRM197) Menhycia® and the Group A and Group C Meningococcal Conjugate Vaccine (CRM197) Menphecia® approved by NMPA in China. The world’s first inhaled COVID-19 vaccine Convidecia Air® has been approved as a booster dose in China, Morocco, and Indonesia. Additional information can be found online at www.cansinotech.com.