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100Days: Thirike, Neestream and Gopi Make their Way into the India Book of Records
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TASMAC Probe: Madras HC Questions ED’s Powers to ‘Seal’ Premises under PMLA, Slams ‘Overreach’
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  • India’s First mRNA Vaccine from Gennova gets DCGI Approval

    By NE Reporter on June 30, 2022

    PUNE:
    Gennova Biopharmaceuticals Ltd., a subsidiary of Emcure Pharmaceuticals Ltd., announced that its mRNA vaccine – GEMCOVAC™-19 – against COVID19 received the Emergency Use Authorization (EUA) from the office of the Drugs Controller General of India (DCGI).

    GEMCOVAC-19™ is the very first mRNA vaccine developed in India and only third mRNA vaccine to be approved for COVID-19 in the world. These vaccines are highly efficacious because of their inherent capacity of being translated into the protein structure inside the cell cytoplasm. mRNA vaccines are considered safe as mRNA is non-infectious, non- integrating in nature, and degraded by standard cellular mechanisms. Notably, this technology provides flexibility to quickly tweak the vaccine for any existing or emerging variants of the virus and this technology platform will empower India to be pandemic ready.

    Gennova’s GEMCOVAC™-19 has reached the primary end point of the Phase III clinical trial. The clinical data was evaluated by the Central Drugs Standard Control Organisation (CDSCO). The vaccine was found to be safe, well-tolerated and immunogenic. Gennova Biopharmaceuticals Ltd. aims to produce around 40 – 50 lakhs of doses per month and this capacity can be quickly doubled.

    Beyond India, Gennova aims at providing sustainable access to low-and middle-income countries around the world to the vaccine to blunt the spread of pandemic.

    NE Reporter

    Covid19Deugs Controller General of IndiaEmcure PharmaceuticalsEmergency Use AuthorizationGEMCOVACGennova Biopharmaceuticals LtsmRNA vaccine

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    • NSE International Exchange (NSE IX) Signs Strategic MoU with Cyprus Stock Exchange
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