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    Kumar Jeetendra

    Sustainable immune dysregulation because of COVID-19 in non-hospitalized patients

    COVID-19, which has killed 1.7 million people globally, doesn’t follow a uniform path. Others, especially those with comorbidities, can create severe clinical disease with atypical pneumonia and multiple system organ failure. Since the first cases were reported in December 2019, the SARS-CoV-2 virus that causes COVID-19 has surged into a pandemic, with cases and deaths

    WHO clears Covid immunization for emergency use

    The World Health Organization says it has cleared the Pfizer-BioNTech coronavirus vaccine for emergency use, meaning poorer countries may soon get access to the shooter already available in Europe and North America. Every country which has a drug regulatory agency will need to issue its own approval for any COVID-19 vaccine, but states with weak

    New UCLA-formed gadget moves mitochondria into at least 100,000 or more beneficiary cells

    Scientists from the UCLA Jonsson Comprehensive Cancer Center have developed a simple, high-throughput way of transferring isolated mitochondria and their associated mitochondrial DNA into mammalian cells. This approach enables researchers to tailor a key genetic component of cells, to study and potentially treat debilitating diseases such as cancer, diabetes and metabolic disorders. A study, published

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    New Delhi: Drug important Glenmark Pharma on Thursday said it has received final approval from the US health regulator for Tadalafil tablets, used to treat erectile dysfunction and enlarged prostate. The business also received two tentative approvals in the US health regulator. Glenmark Pharmaceuticals Ltd has received final approval from the United States Food and

    Emergency use SEC approval for Bharat Biotech Covaxin

    The SEC has recommended Covaxin for emergency use authorisation (EUA), reported news agency ANI quoting government sources. The recommendation, together with rollout modalities, will be taken up from the Drug Controller General of India (DCGI) to get a final decision on the issue. The Subject Expert Committee (SEC) of Central Drugs Standard Control Organisation (CDSCO)

    An incredible achievement in India’s’ scientific fraternity capacity: Bharat Biotech on endorsement for emergency use of covaxin

    Hyderabad, Jan 3 (PTI): Expressing delight over the approval on restricted emergency use of its COVID-19 vaccine Covaxin, Bharat Biotech on Sunday said it has generated excellent safety data with robust immune responses to multiple viral proteins that persist and their goal is to provide global access to populations that need it the most. Ella

    Chemotherapy drug beats remdesivir against Covid in lab tests: Study

    A chemotherapy medication originally developed to treat cancer might potentially be repurposed to inhibit the replication of the novel coronavirus and cure COVID-19, according to a study based on computer simulations and laboratory experiments. The study, published in the journal PLOS Computational Biology, combined multiple computational methods that simulate drug-virus interactions from different, complimentary perspectives.

    FDA confirms resubmission new drug application of Alkermes

    Alkermes plc announced that the U.S. Food and Drug Administration (FDA) has acknowledged receipt of the company’s New Drug Application (NDA) resubmission for ALKS 3831 (olanzapine/samidorphan) for the treatment of adults with schizophrenia and adults with bipolar I disorder, and has assigned the application a new Prescription Drug User Fee Act (PDUFA) target action date