Hindustan Times (East UP)

SII APPLIES FOR DCGI APPROVAL TO USE VACCINE

- HT Correspond­ent letters@hindustant­imes.com

NEW DELHI : The Serum Institute of India, the world’s largest vaccine manufactur­er by volume, has applied to the Drug Controller General of India (DCGI) for emergency use authorisat­ion for the Oxford University-AstraZenec­a Covid-19 vaccine,its chief executive officer Adar Poonawalla said on Monday.

NEW DELHI : The Serum Institute of India, world’s largest vaccine manufactur­er by volume, has applied to the Drug Controller General of India (DCGI) for emergency use authorisat­ion for the Oxford/Astrazenec­a Covid-19 vaccine.

“As promised, before the end of 2020, @SerumInstI­ndia has applied for emergency use authorisat­ion for the first madein-India vaccine, COVISHIELD. This will save countless lives, and I thank the Government of India and Sri @narendramo­di ji for their invaluable support,” said Adar Poonawalla, chief executive officer of Serum Institute of India, in a tweet on Monday.

A trial of the vaccine with 1,600 participan­ts across 15 sites in India is underway. Results from the global studies have shown that it can be 90% effective in preventing an infection when a person receives a half dose and then a full dose.

Serum Institute of India’s move comes on the heels of the US pharmaceut­ical giant, Pfizer, applying for a similar approval with the DCGI. The Pfizer vaccine, which was found to be 95% effective, is likely to cost about five times more than the Oxford vaccine and has to be stored at -70 degrees Celsius.

Oxford University’s Covid-19 vaccine will be priced at Rs 500600, Poonawalla had said during the Hindustan Times Leadership Summit.

“Emergency use authorisat­ion will be for healthcare workers and other frontline workers, and by March- April, the vaccine should be available for use to general public.

Emergency use licensure is based on the positive UK results.

There is a good T-cell and antibody response but nobody at this stage can answer whether these vaccines can protect long-term,” he had said.

The results of the Indian trial is likely to be announced by December.

“As soon as the UK authoritie­s approve of it, we will apply to the

Drugs Controller General of India but initially for limited use. We are stockpilin­g millions of doses to get a head start,” he had said.

He had said that the vaccines could be made available to the general public within three to four months. Serum Institute has entered a manufactur­ing partnershi­p with AstraZenec­a to produce their Covid-19 vaccine.

Serum Institute of India currently has two dedicated facilities with the capacity of manufactur­ing about 50-60 million doses a month that will be scaled up to a 100 million doses by February when two more facilities are likely to be added.

SERUM INSTITUTE OF INDIA’S MOVE COMES ON THE HEELS OF THE US PHARMACEUT­ICAL GIANT, PFIZER, APPLYING FOR A SIMILAR APPROVAL WITH THE DCGI.

 ?? BIPLOV BHUYAN/HT PHOTO ?? A medical worker collects swab sample from a passenger at Hazrat Nizamuddin railway station, in New Delhi on Monday.
BIPLOV BHUYAN/HT PHOTO A medical worker collects swab sample from a passenger at Hazrat Nizamuddin railway station, in New Delhi on Monday.

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