COVAXIN produces immunity, no severe unintended effects in section 2 trials


Aditi Tandon

Tribune News Service

New Delhi, December 23

Data from phase 2 trials of COVAXIN, India’s first indigenous COVID vaccine candidate, has shown the jab was well tolerated across all ages groups, produced cell mediated immune response and did not show any serious adverse event.

Bharat Biotech and ICMR, collaborators for the COVAXIN candidate, have now published the results for phase 1 and phase 2 trials with the late stage phase 3 trials progressing well. The results are still to be peer reviewed though.

“In phase 1 trial, the vaccine (BBV152) produced high levels of neutralising antibodies that remained elevated in all participants three months after the second vaccination. In the phase 2 trial, BBV152 led to tolerable safety outcomes and enhanced cell-mediated immune responses,” the latest data show.

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The researchers are going with the 6 µg formulation for phase 3 efficacy trial after trying the 3 ug formulation in the first two stages.

The phase 2 trial of COVAXIN was a double-blind, randomised, multi-centre, clinical trial involving 380 healthy children and adults who received two vaccine formulations — 3 µg and 6 µg. Two intramuscular doses of vaccines were administered four weeks apart.

“In a follow-up of the phase 1 trial, the vaccine candidate produced high levels of neutralising antibodies that remained elevated in all participants three months at day 104 after the second vaccination. Based on these results, we hypothesise that the vaccine can generate antibodies that may persist for 6-12 months,” the research shows.

Bharat Biotech is among the three companies, including Pfizer and Serum Institute, to have sought emergency use approval in India. The drug regulator has asked it for additional data from phase 3 trials.

Serum Institute has now submitted additional data the regulator had sought last week.

No mutant strain in India yet: Centre

The Centre today dismissed reports of some UK returned travellers showing the mutant COVID 19 strain reported by the UK, and said genome sequencing of samples collected from COVID positive travellers was still underway at government accredited labs.



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