Zydus vaccine given govt panel approval
- 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%.
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 two-dose 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 vaccine-related 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.
The vaccine works by instructing cells to produce the spike protein of the Sars-CoV-2 virus, which elicits an immune response, the ministry of science and technology said in a statement on Friday.
“It is a matter of great pride that today we have the EUA for the world’s first DNA COVID-19 vaccine ZyCoV-D by Zydus developed in partnership with the Department of Biotechnology and supported through Mission COVID Suraksha. The Indian Vaccine Mission COVID Suraksha was launched under the Atma Nirbhar Bharat package 3.0 being implemented by BIRAC, is aimed at the development of safe and efficacious COVID-19 vaccines for public health,” said Dr Renu Swarup, secretary, department of biotechnology, and chairperson, Biotechnology Industry Research Assistance Council.
“We are confident that this will be an important vaccine for both India and the world. This is an important milestone in our indigenous vaccine development mission and positions India on the global map for novel vaccine development,” she added.
There are two vaccine candidates that have been tested among children in India: Bharat Biotech’s Covaxin and Zydus Cadila’s ZyCoV-D. The two are also the only ones of the six now approved in India to be developed indigenously.
The Covaxin trial data in children is still not out, while Zydus Cadila submitted the data to the national drugs regulator along with data from trials held in adult participants on July 1.
The safety and tolerability data of children that was submitted to the regulator for scrutiny showed the tolerability profile was similar to that seen in the adult population, said the company’s managing director, Sharvil Patel, in a press briefing last month.
Patel, last month announced that the company should have a production capacity of about 10-12 million doses per month.
He added that the plug and play technology on which the plasmid DNA platform is based is ideally suited for dealing with Covid-19 as it can be easily adapted to deal with mutations in the virus, such as those already occurring.
The pricing was not discussed as yet but Patel said it would be decided once the regulatory approvals came in as it would depend on doses, technology etc.
“We are extremely happy that our efforts to put out a safe, well tolerated and efficacious vaccine to fight COVID-19 has become a reality with ZyCoV-D. To create the world’s first DNA vaccine at such a crucial juncture and despite all the challenges, is a tribute to the Indian research scientists and their spirit of innovation,” said Pankaj R Patel, chairman, Zydus group.
ZyCoV-D is now the sixth vaccine approved in India for emergency use after Serum Institute of India’s Covishield, Bharat Biotech’s Covaxin, Russian-made Sputnik V, and the American vaccines— Moderna and Johnson and Johnson (J&J).
Meanwhile, American pharma giant Johnson & Johnson (J&J) has sought approval from India’s drugs regulator to conduct clinical trials of its Covid-19 vaccine for the people in the 12-17 age group.
“On 17 August 2021, we submitted an application to the CDSCO to conduct a study of the Johnson & Johnson Covid-19 vaccine in India in adolescents aged 12-17 years,” said a J&J India spokesperson.