The expert panel of the country’s top drug regulator, Director Controller General of India (DCGI), has permitted Hyderabad-based Bharat Biotech to give a third dose of Covaxin to a few volunteers in its clinical trials of the Covid-19 vaccine, sources said.
Sources in the Union Health Ministry said that the Bharat Biotech presented amendments to the subject expert committee of the Drugs Controller General of India (DCGI) in the approved Phase 2 clinical trial protocol for administration of booster dose six months after second dose.
“The firm presented amendments in the approved Phase 2 clinical trial protocol for administration of booster dose after six months after second dose. After detailed deliberation, the committee recommended that the firm should conduct the booster dose study only in a 6 mcg cohort and also should follow up the subjects at least for six months after the third dose,” the SEC said in a minutes of meeting.
Further, Bharat Biotech was asked to present the details of the primary and secondary objectives and various assessments to be carried out in the subjects. “Accordingly, the firm (Bharat Biotech) should submit the revised clinical trial protocol for evaluation,” the SEC said in the meeting that took place on March 23.
In the meeting, Bharat Biotech presented amendments in the approved Phase 3 clinical trial protocol for unblinding of subjects on placebo and addition of another cohort in Brazil which the SEC recommended.