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India Approves Second COVID-19 Vaccine for Children Aged 12-18
India Approves Second COVID-19 Vaccine for Children Aged 12-18
Sputnik International
India has administered more than 1.7 billion doses, including 20 million in the 15 to 18 age group. At present, India uses domestically produced Bharat... 21.02.2022, Sputnik International
2022-02-21T16:49+0000
2022-02-21T16:49+0000
2022-07-19T10:42+0000
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India’s drug regulator has given the green light in emergency conditions to Biological E’s Corbevax vaccine to inoculate pupils between 12 and 18 - roughly one-fifth of India's 1.35 billion population.Corbevax is a recombinant protein sub-unit vaccine made by yeast and the coronavirus spike protein.The emergency use approval comes just as the country is opening up its educational institutions once daily cases fall to less than 20,000.The vaccine's efficacy result has not yet been publicised as the second and third phase trials are still underway among children.The vaccine is administered through an intramuscular route with two doses scheduled 28 days apart and stored at 2 to 8 degrees Celsius.The company has aimed to produce one billion doses by the end of 2022, at a rate of 100 million per month.
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covid-19, vaccine, children, vaccination
covid-19, vaccine, children, vaccination
India Approves Second COVID-19 Vaccine for Children Aged 12-18
16:49 GMT 21.02.2022 (Updated: 10:42 GMT 19.07.2022) India has administered more than 1.7 billion doses, including 20 million in the 15 to 18 age group. At present, India uses domestically produced Bharat Biotech’s Covaxin for adolescents aged between 15 and 18.
India’s drug regulator has given the green light in emergency conditions to Biological E’s Corbevax vaccine to inoculate pupils between 12 and 18 - roughly one-fifth of India's 1.35 billion population.
Corbevax is a recombinant protein sub-unit vaccine made by yeast and the
coronavirus spike protein.
“Once fully vaccinated, children can resume their activities and educational pursuits in schools and colleges without any concerns,” Mahima Datla, Senior Vice-President of Hyderabad-based Biological E Limited, said.
The emergency use approval comes just as the country is opening up its educational institutions once daily cases fall to less than 20,000.
The
vaccine's efficacy result has not yet been publicised as the second and third phase trials are still underway among children.
The vaccine is administered through an intramuscular route with two doses scheduled 28 days apart and stored at 2 to 8 degrees Celsius.
The company has aimed to produce one billion doses by the end of 2022, at a rate of 100 million per month.