CDSCO panel recommends market authorization for Covovax jab as heterologous booster dose

Prakash Kumar Singh, Director of Government and Regulatory Affairs at the Serum Institute of India (SII), had written a letter to the the Drugs Controller General of India (DCGI) recently for the approval to Covovax as a heterologous booster dose for adults in view of the escalating pandemic situation in some countries, an official source told.

The DCGI had approved Covovax for restricted use in emergency situations for adults on December 28, 2021, for those in the 12-17 age group on March 9, 2022, and also in children aged 7- 11 years on June 28, 2022, subject to certain conditions.

Covovax is manufactured by the SII through technology transfer from Novavax.

It has been approved by the European Medicines Agency for conditional marketing authorisation.

It was granted emergency-use listing by the World Health Organization (WHO) on December 17, 2021.

In August 2020, U.S.-based vaccine maker Novavax Inc. had announced a licence agreement with the SII for the development and commercialization of NVX-CoV2373, its COVID-19 vaccine candidate, in India and low-and-middle-income countries.