A study published in The Lancet Infectious Diseases journal assessed 2,714 hospital workers from the All India Institute of Medical Sciences (AIIMS) in New Delhi, from April 15 to May 15, 2021, who were symptomatic and underwent RT-PCR testing for COVID-19. The study was done during the second wave of COVID-19 in the country and the purpose was to find how effective Covaxin is. The Delta variant was the dominant strain in India during the study period, accounting for approximately 80 percent of all confirmed COVID-19 cases.
"Our study offers a more complete picture of how BBV152 performs in the field and should be considered in the context of COVID-19 surge conditions in India, combined with the possible immune evasive potential of the Delta variant," said Dr. Manish Soneja, Additional Professor of Medicine at AIIMS in New Delhi.
Covaxin (BBV152) is a vero cell-derived, inactivated whole-virion vaccine formulated with a novel adjuvant and administered in a two-dose regimen, 28 days apart. In January 2021, BBV152 was approved for emergency use in India for people aged 18, while earlier this month, the World Health Organization (WHO) also added BBV152 to its list of approved emergency use COVID-19 vaccines
Covaxinshot developed by Bharat Biotech in collaboration with the Indian Council of Medical Research (ICMR)-National Institute of Virology (NIV), in July announced the final results of its Phase-III clinical trials. According to the company, the vaccine showed an efficacy rate of 77.8 percent against symptomatic COVID-19, which went up to 93.4 percent against severe symptomatic infection.
In a study published in the journal The Lancet, earlier this month, Bharat Biotech demonstrated Covaxin to be 77.8 percent effective against COVID-19, and 65.2 percent against Delta variant. However, in the latest study researchers at AIIMS acknowledged that the vaccine effectiveness is lower than the efficacy reported by a recently published phase-III randomized control study of BBV152.
Of the 2,714 employees in the study population, 1,617 people tested positive for SARS-CoV-2 infection, and 1,097 tested negative. The adjusted vaccine effectiveness against symptomatic COVID-19 after two doses of BBV152 with the second dose administered 14 or more days before undergoing RT-PCR testing was 50 percent.