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Milestones
2024
2023
2022
2021
2020
2019
2018
2017
2016
2015
2014
2012
2011
2009
10余年沉淀 开启新征程
2024
2024
01
Initiated Phase I clinical trial for VLP-Polio in Australia
02
Acceptance of drug application for registration for the PCV13i
03
Initiated Phase Ⅲ clinical trial for Absorbed Tetanus Vaccine
04
Received positive preliminary results from Phase I clinical trials of the PBPV
05
Obtained clinical trial approval of the Hib Vaccine
06
Initiated Phase Ⅲ clinical trial for Menhycia® in Indonesia
10
VLP-Polio obtained clinical trial approval in Indonesia
10
Grant agreement reached with the Bill & Melinda Gates Foundation for VLP-Polio and related combined vaccine project
2023
2023
01
Convidecia Air® approved in Indonesia
02
Framework Agreement with AstraZeneca on mRNA vaccine
03
IM & IH of Zoster Vaccine approved for clinical trial in Canada
04
Convidecia® registered as a pharmaceutical product in Hong Kong, and obtains Halal Decree in Indonesia
05
Subscription Agreement with Solution Group Berhad
06
Initiated Phase Ⅰb clinical trial for PBPV
07
Bivalent COVID-19 mRNA vaccine, Tdcp Adolescent and Adult, and Tetanus vaccine approved for clinical trial
08
DTcP Infant vaccine entered Phase Ⅲ clinical trial
2022
2022
01
The Recombinant Novel Coronavirus vaccine Convidecia® approved as heterologous b
02
The WHO granted the Emergency Use Listing for the Recombinant Novel Coronavirus
03
Convidecia Air® approved for Emergency Use in Morocco
04
The world's first inhaled COVID-19 vaccine Convidecia Air® approved as heterolog
2021
2021
01
The Recombinant Novel Coronavirus Vaccine Convidecia® received approval in over
02
Menphecia® approved in China
03
Menhycia® approved in China
2020
2020
01
Listed on the Sci-Tech Innovation Board of SSE
02
Completed Convidecia® phase II clinical trial, and launched multi-center phase I
2019
2019
01
Listed on the main board of HKEX
02
NDA for MCV2 was accepted by NMPA
03
NDA for MCV4 was granted with priority review
04
Obtained CTA approval of PCV13i
2018
2018
01
Bacterial vaccine manufacturing facility comes into operation
02
Obtained CTA approval of DTcP
2017
2017
01
Obtained NDA approval of Ad5-EBOV in China
2016
2016
01
Completed Ad5-EBOV phase II clinical trial in Sierra Leone
02
Submitted CTA of PBPV
2015
2015
02
Obtained CTA approvals of MCV2 & MCV4
02
Pilot facility passed European QP inspection
2014
2014
01
Filed CTA for DTcP candidates
02
Obtained CTA approval of Ad5-EBOV and initiated clinical trial
2012
2012
01
Completed the construction of GMP standard pilot plant
2011
2011
01
Incorporated and registered in Tianjin, China
2009
2009
01
Incorporated and registered in Tianjin, China