WHO Seeks 'Additional Clarifications' From Covaxin Before Giving Nod To Emergency Use Listing

The technical advisory group met on Tuesday to review data on Covaxin for the emergency use listing of India's indigenously-made vaccine.

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New Delhi: The technical advisory group of the World Health Organization (WHO) has asked for "additional clarifications" from Bharat Biotech for its COVID-19 vaccine Covaxin to conduct a final "risk-benefit assessment" for Emergency Use Listing of the vaccine.

The technical advisory group met on Tuesday to review Covaxin data for emergency use listing of India's indigenously-made vaccine, PTI reported. 

The technical advisory group will now meet on November 3 for a final assessment.

"The TAG met today (26 October 2021) and decided that additional clarifications from the manufacturer are needed to conduct a final EUL risk-benefit assessment for global use of the vaccine," the WHO said in an emailed response to a question by PTI on the decision regarding the Emergency Use Listing of Covaxin.

"The TAG expects to receive these clarifications from the manufacturer by the end of this week, and aims to reconvene for the final risk-benefit assessment on Wednesday, 3 November," it added.

The Technical Advisory Group for Emergency Use Listing (TAG-EUL) is an independent advisory group that provides recommendations to WHO on whether a Covid 19 vaccine can be listed for emergency use under the EUL procedure. The procedure is dependent on how quickly a company produces the vaccine is able to provide the data required for WHO to evaluate the vaccine's quality, safety, efficacy and suitability for low- and middle-income countries.

Earlier on Tuesday, WHO spokesperson Dr Margaret Harris had said that the technical advisory group that reviews all the data for a potential emergency use listing was reviewing the data for Covaxin.

Bharat Biotech's Covaxin and AstraZeneca and Oxford University's Covishield are the two widely used vaccines in India. The Covaxin has demonstrated 77.8 per cent effectiveness against symptomatic COVID-19 and 65.2 per cent protection against the new Delta variant. In June, the company said it concluded the final analysis of Covaxin efficacy from Phase 3 trials.

Hyderabad-based Bharat Biotech, which has developed Covaxin, had submitted EOI (Expression of Interest) to the WHO on April 19 for the vaccine's Emergency Use Listing (EUL).

The WHO has so far approved Covid-19 vaccines of Pfizer-BioNTech, AstraZeneca-SK Bio/Serum Institute of India, Johnson & Johnson-Janssen, Moderna, and Sinopharm for emergency use.

Last week, the WHO had said it is expecting one additional piece of information from Bharat Biotech regarding Covaxin and emphasised that it has to thoroughly evaluate to ensure vaccines are safe and "cannot cut corners" before recommending a vaccine for emergency use.