Health experts were asked which vaccines they would lie to take between Covishield and Covaxin. (Photo: PIB)
Health experts were asked which vaccines they would lie to take between Covishield and Covaxin. (Photo: PIB)

‘Will take that vaccine...’: Experts explain why Bharat Biotech’s vaccine got approval

Government experts on Tuesday clarified why Covaxin has been given the nod for restricted emergency use.
Hindustan Times, New Delhi | By hindustantimes.com | Edited by Poulomi Ghosh
UPDATED ON JAN 05, 2021 09:38 PM IST

Amid the raging debate over the efficacy of indigenous Covaxin, manufactured by Bharat Biotech in collaboration with the Indian Council of Medical Research and Pune’s National Institute of Virology, the Centre on Tuesday clarified why Covaxin has been given the emergency-use approval though its third phase trial is still going on.

As health secretary, Niti Aayog officials, ICMR director-general Balram Bhargava were present at the press meet, it was asked to them which vaccine they would take between Bharat Biotech’s Covaxin and Oxford-Serum Institute’s Covishield. Niti Aayog member (health) VK Paul answered the question and, holding health secretary Rajesh Bhushan’s hand, said, “I will take the vaccine which my ministry of health will specify for me with great affection, love and gratitude.”

Also Watch | Covid: What led to DCGI nod of Covishield & Covaxin in India? IMCR DG explains

 

Prepared to roll out vaccine within 10 days of emergency-use approval: Health ministry

Covishield data, as presented by the government.
Covishield data, as presented by the government.
Covaxin data, as present by the ministry.
Covaxin data, as present by the ministry.

“All scientific and statutory requirements have been made while giving this approval to vaccines. There is no doubt. These decisions are being taken by experts. Also remember, there is a context. These are not regular authorisation. No country is giving regular authorisation to any vaccine,” Niti Aayog member (health) VK Paul said.

ChatBot, SMS in 12 languages: Health ministry releases new Co-win details

Dispelling doubts over Covaxin, ICMR DG Balram Bhargava said safety, immunogenicity and efficacy reports are required for approval in a non-emergency situation. “Efficacy data is not required for emergency use approval. Immunogenicity data serves as a surrogate for efficacy data in such situation,” Bhargava said.

According to rules, phase two results of clinical data guide experts for approval, which Covaxin has. He also said there have been no safety concerns regarding Covaxin’s trial conducted so far.

Covaxin has also been asked for restricted use in clinical trial mode. Explaining this, Dr Bhargava said, “There has to be consent from the trial participant and there will be follow up.” On Vaccinating children and reopening schools which many states have partially done, Dr Bhargava said, “Adults need to be vaccinated first. So teachers need to be inoculated. And as far as including children in vaccination trial is concerned, the Bharat Biotech trial included those in the age group of 12 to 18 years as well.”

SHARE THIS ARTICLE ON
Close
SHARE
Story Saved
OPEN APP