Government Panel Recommends Market Authorisation For Covovax Jab As Heterologous Booster Dose
The DCGI had approved Covovax for restricted use in emergency situations in adults on Dec. 28, 2021, in the 12-17 age group.
An expert panel of the central drug regulatory authority has recommended market authorisation for Serum Institute of India's Covid vaccine Covovax as a heterologous booster dose for adults who have been administered two doses of Covishield or Covaxin, official sources said on Thursday.
Prakash Kumar Singh, director (government and regulatory affairs) at Serum Institute of India had recently written a letter to Drugs Controller General of India for approval of Covovax heterologous booster dose for those aged 18 years and above in view of escalating Covid-19 pandemic situation in some countries, the sources said.
"The subject expert committee of the CDSCO on Wednesday deliberated on the issue and recommended for market authorisation of Covid jab Covovax as a heterologous booster dose for adults who have been administered two doses of Covishield or Covaxin," an official source said.
The DCGI had approved Covovax for restricted use in emergency situations in adults on Dec. 28, 2021, in the 12-17 age group on Mar. 9, 2022 and also in children aged 7-11 years on Jun. 28, 2022 subject to certain conditions.
Covovax is manufactured through technology transfer from Novavax. It has been approved by the European Medicines Agency for conditional marketing authorization. It was granted emergency-use listing by the World Health Organization on Dec. 17, 2021.
In Aug. 2020, US-based vaccine maker Novavax Inc. had announced a licence agreement with SII for development and commercialization of NVX-CoV2373, its Covid-19 vaccine candidate in India and low-and-middle-income countries.