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Government Commission Has Approved The Zydus Vaccination
Hans News Service | 21 Aug 2021 10:38 AM IST
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Highlights
- India's medicines authority has authorized Zydus Cadila's coronavirus vaccine for anyone aged 12 and up.
- The first dose for use in children and bringing a sixth immunization to India's pandemic kit.
India's medicines authority has authorised Zydus Cadila's coronavirus vaccine for anyone aged 12 and up, authorising the first dose for use in children and bringing a sixth immunization to India's pandemic kit.
The Central Drugs Standards Control Organisation (CDSCO) granted the licence after reviewing results from the manufacturer's phase III clinical studies, which revealed that the vaccine had a 66.6 percent efficacy rate. Officials said that once the immunisation drive is formally increased to protect children, it can be carried out to those under the age of 18.
On Friday, Prime Minister Narendra Modi tweeted and informed and explained thatIndia is waging a full-fledged war against Covid-19. The approval of @ZydusUniverse's world's first DNA-based 'ZyCov-D' vaccine is a testament to India's scientists' inventive drive.
India is fighting COVID-19 with full vigour. The approval for world's first DNA based 'ZyCov-D' vaccine of @ZydusUniverse is a testimony to the innovative zeal of India's scientists. A momentous feat indeed. https://t.co/kD3t7c3Waz
— Narendra Modi (@narendramodi) August 20, 2021
The corporation verified the approval and stated that it has dosages on hand. "...the firm has been granted an emergency use permit... for ZyCoV-D, the world's first Covid-19 plasmid DNA vaccine ZyCoV-D is a three-dose vaccine that will be given on the first day, the 28th day, and the 56th day. India seems to have its first COVID-19 vaccination for children in the country. India also has the first COVID-19 vaccine for children aged 12 to 18 years old, thanks to this approval.
The vaccine is administered using a "painless" intradermal applicator, according to the company, which also aims to seek approval for a two-dose schedule.
According to the company, the capacity of DNA vaccines to activate both the humoral and cellular arms of the adaptive immune system is their fundamental benefit. They are a valuable type of antigen-specific immunotherapy since they are safe, stable, and simple to manufacture.
The expert panel requested further data to enable the company's existing proposal to certify it as a two-dose shot, as per an official who did not want to be identified.
Final approval to carry out the vaccine to children above the age of 12 will be decided by the government's expert vaccination panels, according to a second government official who did not want to be identified.
ZyCoV-D was created in collaboration with the Indian government's Department of Biotechnology as portion of the 'Mission COVID Suraksha,' which saw numerous Indian research institutions pool their resources for testing and regulatory testing.
According to a statement released by the Ministry of Science and Technology on Friday, the vaccine works by encouraging cells to generate the spike protein of the Sars-CoV-2 virus, which triggers an immune response.
However, inIndia, children have indeed been tested on two vaccine candidates: Bharat Biotech's Covaxin and Zydus Cadila's ZyCoV-D. The two are also the only two of the six that have been cleared for development in India. While the Covaxin study data for children has yet to be released, but Zydus Cadila submitted it to the national medicines regulator on July 1 together with data from studies involving adult participants.
According to the company's managing director, Sharvil Patel, in a press event last month, the favorable safety data of minors presented to the regulator for review indicated the tolerability profile was identical to that seen in the adult population.
Patel stated previous month that the company's total production would be around 10-12 million doses per month. He went on to say that the plasmid DNA platform's plug-and-play technology is appropriate for dealing with Covid-19 because it can be easily changed to cope with changes in the virus, including those that have already occurred.
Meanwhile, Johnson & Johnson (J&J) has applied to India's pharmaceuticals authority for permission to begin clinical trials of its Covid-19 vaccine in children aged 12 to 17. After Serum Institute of India's Covishield, Bharat Biotech's Covaxin, Russian-made Sputnik V, and American vaccines Moderna and Johnson and Johnson, ZyCoV-D is currently the sixth vaccine licenced for emergency use in India (J&J).
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