Indian drugmaker seeking Emergency Use Approval for 3-dose Covid-19 vaccine, touted as world’s 1st ‘genetically engineered plasmid DNA’ vaccine

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An Indian drugmaker has applied for Emergency Use Approval (EUA) for its Covid-19 vaccine, which is administered in a three-dose regimen. The firm claims the shot is the first ever plasmid DNA vaccine. In a press statement on Thursday, Indian pharmaceutical giant Zydus Cadila said it had conducted India’s largest Covid-19 vaccine trial to date when testing the effectiveness and safety of its new shot. The trial, it says, took place during the wave caused by the Delta variant. Comment: Black fungus cases surge in India, mostly in patients who recovered from coronavirus The firm stated that they had applied …read more

Source: Sott health news feed

    

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