New Delhi: Managing Director of Zydus Group Dr Sharvil Patel on Saturday said that his firm will soon apply for the Indian drug regulator's approval to conduct trials of ZyCoV-D on children above 2 years and added that it will take another 4-5 months to publish the phase 3 data of the Covid vaccine.
The Ahmedabad-based pharma company has received approval from the Drugs Controller General of India (DCGI) for ZyCOV-D, the world's first and India's indigenously developed DNA-based vaccine for COVID-19 which will be administered in humans including adults and children 12 years and above.
However, the pharma company has not published phase 3 data of trials yet.
"So, the full phase 3 data will show not only the efficacy of the vaccine but also the safety and long-term immunogenicity details which is at least followed up for the next 3-6 months. So, for the full report to be published in a peer-reviewed journal, it will take at least four to five months," Dr Patel told ANI.
Asked about trials conducted on adolescents, he said, "Trials have been conducted at 50 centres across the country. I am not aware of centres for only children. Overall the trials on 28,000 volunteers have been conducted at 50 centres. We have conducted the trials on 1,400 children in the 12-18 years age group."
The Managing Director of Zydus Group said that the firm did not found any severe side effects related to its vaccine in the 12-18 years age group and adults. "In the age group of 12-18 years and adults, we have not seen severe side effects related to the vaccine. We haven't seen any deaths related to the vaccine. We have seen that the vaccine and the placebo which is the non-vaccinated have shown the same kind of mild effects related to the vaccine," he said.
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