Zydus Cadila’s 3-Dose ‘ZyCoV-D’ Vaccine Approved for Emergency Use: Can Your Child Get It?

ZyCoV-D Vaccine: Can Your Child Get It?
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ZyCoV-D Vaccine: Can Your Child Get It?

ZyCoV-D Vaccine: Zydus Cadila’s 3-dose vaccine ‘ZyCoV-D’ has finally been approved for emergency use by the Central Drugs Authority of India. This vaccine is the world’s first and India’s indigenously developed DNA-based vaccine for COVID-19. The Ahmedabad-based company plans to manufacture 10-12 crore doses of ZyCoV-D annually.

Ever since vaccines for adults have been introduced in the country, there have been apprehensions about the safety of children from the contagious virus. This has been a matter of concern for parents across India. Now, the question is, can your child get the ZyCoV-D vaccine?

Yes, if your child is over 12 years old, he/she will be able to get vaccinated. For the first time, apart from adults, adolescents aged 12-18 years will be vaccinated in India. Details about the availability of the vaccine are yet to be announced. Until now, only people 18 years of age or older were eligible for vaccination against the coronavirus.

Meanwhile, another vaccine from Genova, which is an mRNA vaccine, biological E and Novavax’s vaccine candidate, which will be manufactured by Serum Institute of India, are in the pipeline. Recently Dr. Randeep Guleria, Director, AIIMS had said that the data for Phase II and III trials of Bharat Biotech’s Covaxin in the age group of 2 to 18 years is expected by September.

Read also | Zydus Cadila’s ZyCoV-D Vaccine Approved for Emergency Use; can also be used on children

What is the efficacy of ZyCoV-Dvaccine?

Phase III clinical trials were conducted on more than 28,000 volunteers. Interim results of the trials showed a primary efficacy of 66.6 percent for symptomatic RT-PCR positive cases. This is the largest ever vaccine trial for Kovid-19 in India. The vaccine had already demonstrated strong immunogenicity and tolerability and safety profile in previously conducted adaptive phase I/II clinical trials. The Phase I/II and Phase III clinical trials are supervised by an independent Data Security Monitoring Board (DSMB).

How does it react to the body?

When infected, the 3-dose vaccine produces the spike protein of the SARS-CoV2 virus and elicits an immune response, which plays an important role in virus clearance as well as protection against disease. The plug-and-play technology on which the plasmid DNA platform is based can be readily adapted to deal with mutations with viruses, such as those already occurring.

ZyCoV-D Vaccine – In Brief

  • ZyCov-D is an intradermal vaccine, which will be given in three doses.
  • It will be implemented using the Pharmajet needle free system, Tropis, which can lead to a significant reduction in any side effects.
  • ZyCoV-D is stored at 2-8 °C, but has shown good stability at 25 °C for at least three months. The thermostability of the vaccine will help in easier transportation and storage of the vaccine and reduce any cold chain breakdown challenges leading to vaccine wastage.
  • The plasmid DNA platform provides ease of construction with minimal biosafety requirements (BSL-1).
  • Also being a plasmid DNA vaccine, ZyCoV-D does not have any problems associated with vector-based immunity.
  • The plasmid DNA platform allows to quickly generate new constructs to combat mutations in the virus, such as those that are already occurring.

Read also | Do I need a booster if I have had the Johnson & Johnson vaccine?

Read also | Johnson & Johnson’s single-dose COVID vaccine approved for emergency use in India

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