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No approval yet for Bharat Biotech’s COVID-19 vaccine Covaxin: Expert panel seeks more data

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    Published on 01 January 2021
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    Millions of Indians have been waiting with bated breath for the outcome of the meeting today on vaccine approval for the country. The decisions taken at the meeting are out now. The Subject Expert Committee of the Central Drug Standard Control Organisation has held that the data provided by Bharat Biotech for its COVID-19 vaccine ‘Covaxin’ is not sufficient for grant of emergency use approval and has asked for more information, top sources said. Meanwhile, the DCGI, on Thursday, had hinted at the approval of a vaccine and said that the country will have a “Happy New Year with something in hand”. Also Read – Expert panel approves emergency use for Oxford COVID-19 vaccine in India

    Covishield becomes first vaccine to get approval in India

    Earlier today, the expert committee, which is tasked with vetting COVID-19 vaccine proposals, recommended emergency licensure for the Serum Institute of India-manufactured ‘Covishield‘. It has now become the first vaccine to secure recommendation for emergency use in India. The Pune-based Serum Institute has partnered with Oxford-AstraZeneca for conducting clinical trials and manufacturing ‘Covishield’ while Bharat Biotech has collaborated with the Indian Council of Medical Research (ICMR) for ‘Covaxin’. Also Read – Pfizer, Moderna COVID-19 vaccines safe for people with food allergies, say experts

    Official sources said that the panel’s recommendation has been sent to DCGI V.G. Somani for approval. Once the approval comes, it will clear the way for the rollout of the vaccine in India, which incidentally has the highest number of infections in the world, after the US. Ministry sources said that the rollout will begin from January 6. The UK and Argentina have already approved Covishield. More than five crore doses of the vaccine have already been stockpiled by its manufacturer, the Pune-based Serum Institute of India. Also Read – Sustained cellular immune dysregulation in patients recovering from COVID-19

    Three vaccine candidates in the fray

    The committee had convened a meeting to take a call on the emergency use authorisation sought by the Serum Institute, Bharat Biotech and America’s Pfizer for their coronavirus vaccines candidates. Pfizer was the first one to apply for the accelerated approval on December 4, followed by the Serum Institute and Bharat Biotech on December 6 and 7, respectively.

    Decision comes a day before dry run of vaccines in India

    The meeting comes a day before dry run of the vaccine is slated to commence in all the states and Union Territories to equip the administration in management of vaccine supply, storage and logistics including cold chain management. The Central government plans to vaccinate nearly 30 crore people in the first phase of drive. It will be offered to one crore healthcare workers, along with 2 crore frontline and essential workers and 27 crore elderly, mostly above the age of 50 years with co-morbidities.

    (With inputs from IANS)

    Published : January 1, 2021 10:42 pm

    Source: | This article originally belongs to thehealthsite.com

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