tricision and China Resources Biopharmaceutical Forge Strategic Alliance on mRNA Prophylactic Vaccines for Infectious Diseases
Beijing tricision Biotech Co., Ltd.
(tricision) and China Resources Biopharmaceutical Co., Ltd. (China
Resources Biopharmaceutical) have announced that Yixing
Chenggong New Drug Development Co., Ltd. (Chenggong New Drug), a
wholly-owned subsidiary of tricision, has entered into a strategic cooperation
agreement with China Resources Biopharmaceutical for the co-development of
an mRNA Respiratory Syncytial Virus (RSV) vaccine.
The partnership, founded on principles
of mutual benefit, complementarity, and innovation, leverages
tricision's proven capabilities in its clinically validated plasmid and
Messenger RNA (mRNA) platforms, nanotechnology and delivery systems, and Chemistry,
Manufacturing, and Controls (CMC) platform, combined with China
Resources Biopharmaceutical's industry-leading position and clinical
development expertise. Together, the two parties will pursue deep collaboration
on prophylactic mRNA vaccines for infectious diseases.
RSV: A Persistent Global Health
Challenge
Respiratory Syncytial Virus (RSV) is a negative-sense, single-stranded RNA virus belonging to
the genus Pneumovirus of the family Paramyxoviridae. First isolated from
chimpanzees in 1956, it was named for its association with respiratory
infections and its ability to fuse infected cells. RSV imposes a significant
disease burden on infants, young children, and the elderly. Treatment for
high-risk populations is primarily symptomatic and supportive, making prevention
the cornerstone of RSV management. Natural infection does not induce
durable immune memory against conserved immunogens, so RSV immunoprophylaxis
relies on passive prevention (antibody drugs) or active prevention
(prophylactic vaccines). Despite more than 60 years of research, no
broadly effective preventive or therapeutic agent has been approved globally.
Differentiated Technology: tricision's
mRNA RSV Vaccine Candidate
The RSV vaccine being co-developed by
Chenggong New Drug and China Resources Biopharmaceutical is built on
tricision's immunology-driven plasmid platform, which has undergone extensive
screening and optimization. The vaccine is produced using the clinically
validated mRNA platform, with formulation optimization via nanotechnology and
the Lipid Nanoparticle (LNP) platform, and rapid pilot-scale
production through the CMC platform. The nanoliposome C2 molecule employed—tricision's
proprietary patented liposome—features a unique spatial structural design
that offers advantages including structural stability, safety, and high
membrane fusion efficiency. Recent analytical data indicate that this
mRNA RSV vaccine demonstrates significant technical and market advantages in
safety and efficacy compared to various international RSV vaccine
products.
Building on an Existing Collaboration
This strategic cooperation between China
Resources Biopharmaceutical and tricision follows their previous collaboration
in January 2023 on therapeutic drug co-development for Glioblastoma
Multiforme (GBM), marking a second strategic partnership—this time on mRNA
vaccine R&D and commercialization for RSV. Both projects represent globally
challenging research areas, entailing significant scientific hurdles, but
also substantial opportunities and long-term promise.
Integrated Platform Advantage
tricision's core "One Body,
Two Wings" technology architecture—comprising nucleic acid
technology, Nanodelivery Platform (NP), and Cell Delivery
Platform (CDP)—along with over 40 patented technologies including triVAC,
C2 liposome, mRNA lyophilization technology, and Needle-Free Injection
(NFI), enables rapid product development while also offering platform
advantages in product design, process development, stability, safety, and high
delivery efficiency.
As the innovative biologics platform of the China Resources Pharmaceutical Group, China Resources Biopharmaceutical's renewed collaboration with tricision aims to accelerate the domestic R&D and market launch of mRNA nucleic acid drugs, ensuring that innovative technologies and therapies enter the market safely and effectively, safeguarding public health, and jointly advancing China's innovative biopharmaceutical development.
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Time:2026-07-10
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