Hyderabad: The Drugs Controller General of India has granted restricted emergency use authorization (EUA) to Biological E’s COVID-19 vaccine Corbevax for the 12 to 18 years age group, subject to certain conditions, official sources said on Monday.
However, the government has not taken a decision yet on vaccinating those aged below 15 years.
This is the third vaccine to have received EUA from the Drugs Controller General of India (DCGI) for the age group of 12-18 years after Zydus Cadila’s ZyCoV-D and Bharat Biotech’s Covaxin.
At present, India is using Covaxin to vaccinate adolescents in the 15 to 18 years age group.
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The health ministry recently had said the additional need for vaccination and inclusion of population for vaccination is examined constantly.
The DCGI’s approval comes after the Subject Expert Committee on COVID-19 of the CDSCO on February 14 recommended granting restricted EUA to Corbevax for the 12 to 18 years age group after deliberating on Biological E’s application.
The DCGI had approved Corbevax, which is India’s first indigenously developed RBD protein sub-unit vaccine against COVID-19, for restricted use in emergency situations in adults on December 28. It has not been included in the country’s vaccination drive.
”The DCGI on Monday granted restricted EUA to Corbevax for the 12 to less than 18 years age group subject to certain conditions,” an official source said.
Health Minister Mansukh Mandaviya tweeted, ”The @CDSCO_INDIA_INF has granted emergency use authorization to COVID-19 vaccine #CORBEVAX for 12-18 year age group. It is India’s 1st indigenously developed Receptor Binding Domain Protein sub-unit vaccine against COVID-19. This will further strengthen our fight against COVID19.”
Mahima Datla, Managing Director, Biological E Limited, said: “We are pleased with this significant development, which helps extend the reach of our vaccine to the age group of 12 to 18 years in our country.” With this approval, we are even more closer to overcoming our global fight against the COVID-19 pandemic, she said.
In an application sent to the DCGI on February 9, Srinivas Kosaraju, the head of quality and regulatory affairs at Biological E Limited, had said the firm had received approval for conducting phase 2/3 clinical study of Corbevax among children and adolescents aged 5-18 years in September.
”Based on the no-objection certificate, Biological E has initiated the clinical study in October 2021 and has evaluated the available safety and immunogenicity results of the ongoing phase 2/3 study, which indicated that the vaccine is safe and immunogenic,” he said.
”The proposed application is for obtaining permission for restricted use in an emergency situation in adolescents aged 12 to less than 18 years based on interim results (of the ongoing phase 2/3 clinical study) considering the current pandemic and widespread of COVID-19 vaccine in India,” Kosaraju had said in the application.
The Corbevax vaccine is administered through the intramuscular route with two doses scheduled 28 days apart and is stored at two to eight degrees Celsius temperatures and presented as 0.5 ml (single dose) and 5 ml (10 doses) vial pack.
According to the health ministry, the company has conducted phase 1/2 and 2/3 clinical trials of its COVID-19 vaccine in the country.
Further, it has conducted a phase 3 active comparator clinical trial to evaluate superiority against the Covishield vaccine, it said.
Mahima Datla said, ”Once fully vaccinated, children can resume their activities and educational pursuits in schools and colleges without any apprehension.”
She thanked all the participants in the clinical trials, Biotechnology Industry Research Assistance Council (BIRAC) and Department of Biotechnology of the Union government, Translational Health Science and Technology Institute (TSTHI), and the principal investigators and clinical site staff who have extended their support during the last several months.