NEW DELHI: As many as eight vaccine candidates for Covid-19 are under different stages of clinical trials which could be ready for authorisation in near future, the ministry of health and family welfare informed in a press briefing on Tuesday.
The ministry informed that the eight vaccines include Astrazeneca and Oxford university developed and Serum Institute of India manufactured Covishield, Covaxin by Bharat Biotech Limited, ZyCoV-D by Zydus Cadila, Russian vaccine candidate Sputnik-V, NVX-CoV2373 by SII, HGCO19 by Geneva, and two unlabeled vaccines—Recombinant Protein Antigen based vaccine by Biological E Limited—and Inactivated rabies vector platform by Bharat Biotech.
While the former five vaccine candidates have entered either phase II or phase III clinical trials, the latter three are in pre-clinical trial phases, the ministry informed.
Meanwhile, two vaccines candidates — Covishield and Covaxin — are in the third stage of clinical trials. They have applied for emergency use authorisation to the Drug Controller General of India (DCGI). Their application is pending for the review which is expected to happen on Wednesday by the subject expert committee (SEC) for the vaccines.
However, the application for the emergency use authorisation (EUA) of Covaxina and Covishied has followed after Pfizer’s BNT162b2 which was the first vaccine candidate to seek the EUA.
Union health secretary Rajesh Bhushan informed that few of the vaccine candidates may receive licence for authorisation in next few weeks. “The complete immunization in all the eight candidates would require 2-3 doses of it inoculated at the gap of 3 to 4 weeks,” he added. He also cautioned that Covid precautions must be undertaken even after the vaccination.
Pfizer India had submitted an application on 4 December to the DCGI seeking emergency use authorisation (EUA) for its Covid-19 vaccine in India. Following which, Serum institute also filed for the EUA while the Bharat Biotech’s applied for the same on Monday.
Pfizer applied for EUA in India after it received permission for temporary authorisation for its emergency use in the UK last week. The UK on Wednesday became the first country to approve the Pfizer/BioNTech vaccine against Covid-19, with the UK regulator Medicines and Healthcare products Regulatory Agency granted approval to Pfizer’s vaccine for EUA on Wednesday last week.
Pfizer’s vaccine would require -70 degree celsius of temperature for its storage.
With IANS inputs
