Bharat Biotech Applies for Vaccine's Emergency Approval Again

Hyderabad-based Bharat Biotech has applied again to the Drug Controller General of India for the emergency use authorization of COVID-19 vaccine. Bharat Biotech is developing the country's indigenous coronavirus vaccine in collaboration with the ICMR.

Bharat Biotech in Hyderabad has once again applied to the Drug Controller General of India for the emergency use authorization. Emergency Use Authorization is a mechanism to facilitate the availability and use of medical countermeasures, including vaccines, during public health emergencies. //

"The company applied for the emergency use authorization in the evening," a company source told IANS.

Coronavirus
Coronaviruses infect animals, humans, and birds. Human coronaviruses, such as SARS, MERS, and 2019-nCoV cause respiratory distress and even death. The S protein is the infectious agent of the virus.

‘Hyderabad-based Bharat Biotech, which is developing the country's indigenous coronavirus vaccine in collaboration with the Indian Council of Medical Research, applied again to the Drug Controller General of India for the emergency use authorization.’

Bharat Biotech had first applied for the emergency use authorization of its vaccine on December 7 and presented its proposal, along with the interim safety and immunogenicity data of Phase 1 and 2 clinical trials.

The Central Drugs Standard Control Organization's (CDSCO) expert panel had, however, recommended that the firm should present the safety and efficacy data from the ongoing Phase 3 clinical trial in the country for further consideration.

Bharat Biotech's COVAXIN, an inactivated vaccine candidate, is currently undergoing Phase 3human clinical trials on 26,000 volunteers over 25 centers across India, after having undergone Phase 1 and 2 trials involving 1,000 volunteers.

COVID Vaccine: Moderna Coronavirus Vaccine All Set For FDA Emergency Approval
A high powered vaccine advisory panel has endorsed Moderna's COVID-19 vaccine for emergency use approval (EUA) by the FDA.

Meanwhile, the Serum Institute of India (SII) has also submitted the additional data asked by the DCGI determining safety and immunogenicity of its COVID-19 vaccine candidate, Covishield.

America's Pfizer was the first to apply on December 4, followed by Pune-based SII and Bharat Biotech who applied on December 6 and 7, respectively. Pfizer had, however, requested more time to make presentation before the committee.

Coronavirus Vaccine Will be Free in Kerala
COVID-19 vaccine will be provided free in Kerala, said Kerala Chief Minister Pinarayi Vijayan. He said the day saw 5,949 people turn Covid positive after 59,690 samples was send for testing.

Pfizer, whose vaccine has been authorized in the US, the UK and Canada, has written to DCGI seeking a fresh date to present its case for the EUA of their vaccine candidate BNT162b2, after it failed to present its data before the vaccine reviewing committee of the CDSCO earlier.

India is likely to have a Covid-19 vaccine approved for emergency use before December end as CDSCO's expert panel is set to review the application of SII, Bharat Biotech and Pfizer for emergency use authorization.

Coronavirus Vaccine to be Rolled Out Within 3 Months in UK
The new COVID-19 vaccine developed by Oxford University scientists could be rolled out in as little as three months in the UK, a report said.

Source-IANS