Hindustan Times (Patiala)

Zydus vaccine given govt panel approval

- Rhythma Kaul letters@hindustant­imes.com

NEW DELHI: India’s drugs regulator approved a coronaviru­s vaccine by Zydus Cadila for anyone aged 12 and above, clearing the first shot for use in children and adding a sixth inoculatio­n in India’s toolbox to fight the pandemic.

The approval was given by Central Drugs Standards Control Organisati­on (CDSCO) after its experts assessed results from the company’s phase III clinical trials that showed the vaccine to have an efficacy of 66.6%. Officials said it can be rolled out to those under the age of 18 once the inoculatio­n drive is officially expanded to cover children – at present, it is only for adults.

“India is fighting Covid-19 with full vigour. The approval for world’s first DNA based ‘ZyCov-D’ vaccine of @ZydusUnive­rse is a testimony to the innovative zeal of India’s scientists. A momentous feat indeed,” Prime Minister Narendra Modi tweeted on Friday.

The company confirmed the approval and said it has already stockpiled doses. “…the company has received the emergency use authorisat­ion… for ZyCoV-D the world’s first plasmid DNA vaccine for Covid-19. ZyCoV-D is a three-dose vaccine which will be administer­ed first on day zero, day 28th and then on the 56th day. With this approval, India now has its first COVID-19 vaccine for the adolescent­s in the 12-18 age group…,” the company said.

It said the vaccine is delivered via a “painless” intraderma­l applicator and added that it plans to seek approval for a twodose regimen of the vaccine. “The main advantage of DNA vaccines is their ability to stimulate both the humoral and cellular arms of the adaptive immune system. They are a valuable form of antigen-specific immunother­apy, as they are safe, stable and can be easily produced,” the company said.

An official, who asked not to be named, said the expert panel sought more data to allow the company’s existing request to approve it as a two-dose shot.

A second government official, who asked not to be named, said final approval to roll-out the vaccine to children above the age of 12 will be taken by government’s expert committees on vaccinatio­n.

“The emergency use approval has come for the Zydus vaccine for use in 12 year olds and above but it will be the call of the experts on panels such as NTAGI (National Technical Advisory Group on Immunisati­on) and NEGVAC (National Expert Group on Vaccine Administra­tion for COVID-19), who decide on Covid-19 vaccinerel­ated matters, whether to allow Covid-19 vaccinatio­n in children; and when. Even if the experts allow it, orders will have to be placed -- there is an entire procuremen­t process that needs to be followed. Regulatory approval is just a part of the process,” this person said.

ZyCoV-D was developed in partnershi­p with the government’s Department of Biotechnol­ogy under the ‘Mission COVID Suraksha’, which involved the pooling of resources by several Indian research institutio­ns for developmen­t and clinical trials.

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