Bharat Biotech applies for emergency use authorisation for Covaxin

The company is conducting a 26,000 subjects phase 3 efficacy trial in India to determine the efficacy of its candidate

Covaxin, bharat biotech, covid, coronavirus, vaccine, drugs, medicine, pharma
The company has Phase 1 and phase 2 data ready and would submit the interim data from large scale efficacy trials to the DCGI for review.
Sohini Das
1 min read Last Updated : Dec 08 2020 | 1:12 AM IST
After Pfizer and Serum Institute of India, Hyderabad-based Bharat Biotech has applied for an emergency use authorisation for its investigational vaccine candidate, Covaxin, to the Indian regulator. The firm is conducting its Phase 3 trial, involving 26,000 participants. 

This is one of the largest efficacy trials held in the country. The firm has Phase 1 and Phase 2 data ready and will submit the interim data from the large-scale efficacy trials to the Drug Controller General of India.

Officials from the Central Drugs Standard Control Organization and the Indian Council of Medical Research have been in touch with the firm.

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Topics :CoronavirusCoronavirus VaccineBharat BiotechICMRDrug Controller General of India

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