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Home >Products >Marketed Products > Recombinant COVID-19 Vaccine (Adenovirus Type 5 Vector) Convidecia®
Convidecia – Single shot for faster protection
  • name:Recombinant COVID-19 Vaccine(Adenovirus Type 5 Vector)
Timeline
2021
  • 04
    Obtained Emergency Use Authorization in Chile
  • 03

    Obtained approval to conduct a clinical trial for inhaled version of COVID-19 vaccine in China

    Obtained Emergency Use Authorization in Hungary

  • 02

    Obtained approval in China

    Obtained Emergency Use Authorization in Pakistan

    Obtained Emergency Use Authorization in Mexico

    Successfully met pre-specified primary safety and efficacy criteria in interim analysis of phase III trial

2020
  • 09
    Launched global multicenter phase III clinical trial
  • 07
    Published positive results of the phase II clinical studies in the Lancet
  • 06

    Obtained military specially-needed drug approval

    Obtained manufacturing approval

  • 05
    Published positive results of the phase I clinical studies in the Lancet
  • 04
    Launched phase II clinical trial
  • 03
    Launched phase I clinical trial
  • 01
    Initiated the COVID-19 project
Convidecia
Convidecia is a Recombinant Novel Coronavirus Vaccine (Adenovirus Type 5 Vector) co-developed by CanSinoBIO and the Beijing Institute of Biotechnology, Academy of Military Medical Sciences. Convidecia received conditional approval by China NMPA on Feb 25th, 2021.
The main features are:
1 dose, 14 day rapid protection 1 dose, stimulates humoral and cellular immunity, providing dual protection 1 dose, more cost-effective
14 Days: 68.83% effective in preventing all symptomatic COVID-19 disease and 95.47% effective in preventing severe COVID-19 disease28 Days: 65.28% effective in preventing all symptomatic COVID-19 disease and 90.07% effective in preventing severe COVID-19 disease
Convidecia news
COVID-19 is a new acute respiratory infectious disease and has become a public health emergency of international concern. With strict prevention and control and medical treatment, China has successfully contained COVID-19 domestically, with only occasional localized outbreaks and few imported cases. However, as the pandemic continues to spread globally, China still faces the risk of COVID-19 outbreaks before mass immune protection is established.
FAQ
Q1
Why did CanSinoBIO choose to use the technological platform of adenovirus vector to develop COVID-19 vaccine?
Soon after the outbreak of COVID-19, we evaluated platforms for COVID-19 vaccine development, including viral vector and mRNA-based technologies. Due to the severity of the pandemic and the urgent need for an effective vaccine against COVID-19, we wanted a technological platform that would enable us to develop a vaccine with a good safety and efficacy profile in a timely manner. We decided to use the adenovirus vector for COVID-19 vaccine development because we have an established technological platform for the adenovirus vector, based on which we have already developed a TB booster, CVE vaccine, Zika vaccine and the recombinant Ebola vaccine, jointly developed with the Beijing Institute of Biotechnology, Academy of Military Medical Sciences, and which was approved in China in 2017. Leveraging the established technological platform of the adenovirus vector and our experienced team, the development of Convidecia made rapid progress. The project was initiated on January 20th, 2020, and entered Phase I trials on March 16th, 2020, making it the first of its kind worldwide to enter clinical study.
Q2
What is the mechanism of the adenovirus vector used in Convidecia?
Genes related to virus replication are removed from the adenovirus type 5 vector used in Convidecia so that the vector is replication-defective in the human body. A gene sequence encoding the COVID-19 spike protein (S protein) is inserted into that location. The viral vector serves as a carrier that delivers the gene sequence of S protein into cells. Once it has entered a cell, the gene sequence is transcribed to express S protein, which in turn serves as an antigen that stimulates the immune system to recognize the COVID-19 virus.
Q3
What precautions should I take before and after getting the COVID-19 vaccine?
①Before vaccination, your doctor will make inquiries about your medical history and health conditions to decide if you are eligible to receive the vaccine. Please make honest disclosures. ②After vaccination, all individuals should be observed for 30 minutes to monitor if any adverse reaction occurs. On the day of vaccination, please keep the injection site dry and clean, and we recommend being well rested. ③Within one week after vaccination, please avoid exposure to your known allergens or other common allergens and minimize the use of alcohol and the intake of spicy food. It is recommended to have a light diet and adequate fluid intake.
Q4
Who is contraindicated or should postpone getting the COVID-19 vaccine?
Please see the label instructions of respective COVID-19 vaccines for detailed contraindications and strictly follow the instructions. In general, individuals with a known history of severe allergic reactions to any component of the vaccine are contraindicated. Additionally, individuals who have fever, an acute disease or a breakout of an underlying chronic disease should postpone the vaccination.。
Q5
Should individuals wear a mask after receiving the COVID-19 vaccination?
Before mass vaccination reaches a higher level of immune protection, one should maintain awareness to prevent infection and transmission and should maintain personal hygiene habits. Vaccinated or not, one should still wear a mask indoors and follow specified prevention and control measures.
Q6
Are there adverse reactions to the COVID-19 vaccine?
①The most common adverse reactions after vaccination are fever, redness, swelling and pain in the vaccination site. Usually, a reaction can be relieved by itself within 96 hours, and no special treatment is required. ②If the symptoms are serious or the severity cannot be judged by yourself, one should seek medical treatment immediately and report to the doctor at the vaccination site. ③According to previous experience, serious adverse reactions will occur within 30 minutes after vaccination. Please observe as required and ask for the doctors on site.
Q7
Should individuals who have a history of allergic reactions get a COVID-19 vaccine?
Any history of allergies will be considered as a precaution. Individuals with a known history of severe allergic reactions to any component of the vaccine are contraindicated. For individuals with common allergies to pollen with symptoms such as blocked nose, runny nose or rash, it is recommended to avoid getting the COVID-19 vaccine during an ongoing allergic reaction or follow your doctor’s instructions in the case of mild symptoms.