Zydus Cadila’s application to the Indian regulator for an accelerated nod or emergency use authorization (EUA) for its COVID-19 vaccine takes the world a step closer to the first plasmid DNA vaccine approved for human use.
While vaccines made with recombinant DNA technology, like Recombivax and Engerix-B for hepatitis B, have been approved by the US Food and Drug Administration (FDA) and veterinary DNA vaccines are in use, the contender
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