Zydus Cadila's 3-dose vaccine gets emergency use approval in India


New Delhi, Aug 20 (IANS): Zydus Cadila's three-dose indigenous Covid-19 vaccine ZyCoV-D, the world's first DNA-based Covid vaccine that can be administered to people aged 12 and above, on Friday received emergency use authorisation (EUA) in India, an official statement said.

The Central Drugs Standard Control Organisation's (CDSO) Subject Expert Committee (SEC) granted the EUA.

The Science and Technology Ministry statement said: "Zydus Cadila has received approval for Emergency Use Authorisation (EUA) from the Drug Controller General of India (DCGI) for ZyCoV-D today."

ZyCoV-D is a first of its kind DNA vaccine that produces the spike protein of the SARS-CoV-2 to elicit an immune response. It is an intradermal vaccine that has to be applied using a 'needle-free injector', which, the manufacturer says, will help in reducing side effects.

Developed in partnership with the Department of Biotechnology, under 'Mission COVID Suraksha' and implemented by the BIRAC, ZyCoV-D has been supported under Covid-19 Research Consortia through National Biopharma Mission for Preclinical Studies, Phase 1 and Phase 2 Clinical Trials and under the Mission COVID Suraksha for Phase 3 Clinical Trial.

This 3-dose vaccine, when injected, produces the spike protein of the SARS-CoV-2 virus and elicits an immune response, which plays a vital role in protection from disease as well as viral clearance. The plug-and-play technology on which the plasmid DNA platform is based can be easily adapted to deal with mutations in the virus, such as those already occurring.

The interim results from Phase 3 Clinical Trials, involving over 28,000 volunteers, showed primary efficacy of 66.6 per cent for symptomatic RT-PCR positive cases. This has been the largest trial so far in India for Covid-19 vaccines.

The vaccine had already exhibited robust immunogenicity and tolerability and safety profile in the adaptive Phase 1/2 clinical trials carried out earlier. The Phase 1/2 and Phase 3 clinical trials have been monitored by an independent Data Safety Monitoring Board (DSMB).

 

  

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Comment on this article

  • Dev, Mangalore

    Sat, Aug 21 2021

    In the first place the present pandemic is never dangerous to kids below 25 years. As such introducing unproven experimental vaccines is more dangerous than seasonal flu labelled as covid.. Just like mRNA vaccines this too produces spike proteins in the body, which were found to be more toxic than the virus itself. This vaccine too produces spike proteins and long term study is needed before using kids as human guinea pigs for companies greed. I had predicted this last month itself- now 12 to 18 kids will be illegally mandated before opening the schools. Next target will be kids born to 10 years by evil globalists and corrupt politicians.

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  • John, Mangalore

    Fri, Aug 20 2021

    Anything tinkering with human DNA risks of Autism specially in growing children? why hurry ? Test it for a year or two then release? As Research on aborted fetal cells used in vaccines causes autism or double, confusing personality..... Both of these, World Renowned Genetics Doctor Dr. Theresa Deishe and Vaccine researcher Pamela Acker Correlate Autism with fetal cell / DNA fragments in vaccines in following referenced articles at Ref: https://vaccineimpact.com/2017/world-renowned-genetics-doctor-sees-relationship-between-fetal-cells-used-in-vaccines-and-increasing-autism-rates/ Ref2: https://www.lifesitenews.com/opinion/a-hill-worth-dying-on-expert-explains-how-aborted-baby-cells-taint-covid-vaccines

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