Significant Progress Made on the Trivalent Recombinant Protein COVID-19 Vaccine against Subvariants including XBB.1.5 and BA.5 by WestVac Biopharma
PR99587
CHENGDU, China, Feb. 20, 2023 /PRNewswire=KYODO JBN/ --
Recently, with the support of the National Key R&D Program of China, following
the clinical trial approval for Recombinant Variant COVID-19 Vaccine (Sf9 cell)
approved by NMPA, WestVac Biopharma (Guangzhou) Co., Ltd. (hereinafter referred
to as "WestVac Biopharma (Guangzhou)") has made significant progress on the
development of the trivalent recombinant protein COVID-19 vaccine against the
latest prevalent subvariants including XBB.1.5 and BA.5, which is one of the
first trivalent recombinant protein vaccines targeting XBB.1.5 worldwide.
Taking advantage of the rapid response of the internationally advanced insect
cell expression platform in recombinant protein vaccine production, WestVac
Biopharma (Guangzhou) has constructed the vector within one month, and produced
the trivalent recombinant protein vaccine of high purity and quality for human
use. It is an entirely synthetic vaccine. The subunit vaccine antigen is
precisely designed based on the structure of the targeting S-RBD and HR protein
of XBB.1.5 and BA.5 subvariants, and can self-assemble into stable trimeric
protein particles. Study revealed that the vaccine induced high titers of
neutralizing antibodies against Omicron XBB.1.5, BQ.1, BF.7, BA.5, BA.2.75 and
other subvariants, suggesting that it is a broad-spectrum COVID-19 vaccine
against multiple prevalent subvariants at home and abroad such as XBB.1.5,
BQ.1, BF.7 and BA.5. At present, WestVac Biopharma is proactively engaged with
the national authorities, and striving to meet the national approval
requirements as soon as possible for the trivalent recombinant protein
vaccine.The mission is to use WestVac BioPharma's power to aid in the fight
against new variants of novel coronavirus!
WestVac Biopharma (Guangzhou) is a wholly-owned subsidiary of WestVac Biopharma
Co., Ltd. located in the Innovative Vaccine Production Base in the Knowledge
City of Guangzhou Economic Development Zone. With the production lines of a
combined 5000L to be constructed soon for insect cell recombinant protein
vaccine and nasal spray vaccine, it will have an annual production capacity of
500 million doses of vaccines.
WestVac Biopharma Co., Ltd., the parent company, is an innovative
biopharmaceutical company integrating vaccine R&D, production and sales. From
2021 to 2022, WestVac Biopharma was selected successfully on the list of
unicorn companies for two consecutive years. Coviccine® --Recombinant COVID-19
Vaccine (Sf9 cell) developed by WestVac Biopharma has shown satisfactory safety
and immunogenicity in clinical trial with 70.95% protective efficacy against
Omicron subvariants, which is one of the most effective vaccines in preventing
symptomatic COVID-19 cases with Omicron subvariants in the world. In December
2022, Coviccine® has been approved by the national authority for emergency use
and already been in the bidding process and supplied for vaccination in
multiple provinces. In the meantime, Recombinant Variant COVID-19 vaccine (Sf9
cell) developed by WestVac Biopharma has recently received the Approval for
Clinical Trial by NMPA, the phase I/II clinical trials will soon begin.
SOURCE: WestVac BioPharma Co., Ltd.
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Caption: WestVac BioPharma Co., Ltd.
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