Tpoxx, which has been prescribed to tens of thousands of patients afflicted with monkeypox, works by targeting a single protein found on monkeypox, smallpox and similar viruses.
The FDA's earlier decision, in April, to put on hold the trials was based on the US firm's decision to voluntarily implement a temporary pause in dosing participants of the jab.
Maharashtra: Cases filed against e-commerce firm after FDA detects illegal sale of abortion kits in parts of state
FDA Assistant Commissioner Ganesh Rokade said the administration had received information that abortion drugs were being sold illegally on Meesho.com, an online portal.
The WHO had earlier suspended supply through UN agencies of Coavaxin after inspectors identified good manufacturing practice deficiencies in the company's pharma plant.
WHO had earlier suspended the supply of Covaxin through US procurement agencies, after its inspectors identified GMP deficiencies in the Bharat Biotech's manufacturing plants.
Moderna said its request for an additional dose was based on “recently published data generated in the United States and Israel following the emergence of Omicron.”
According to the FDA, the state has 51,425 injections of Remdesivir, 20,25,381 Favipiravir tablets and their Nagpur lab has currently stored 1.97 lakh injections that are ready to be distributed.
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