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    US to pay $2.1 billion to Sanofi, GSK in COVID-19 antibody bargain

    The US government will pay $2.1 billion to Sanofi SA and GlaxoSmithKline Plc to get COVID-19 vaccines to pay 50 million individuals and to underwrite the drug manufacturers’ testing and manufacturing, the companies said on Friday. The award is the biggest yet from’Operation Warp Speed’, the White House initiative aimed at accelerating access to treatments

    Zydus Cadila gets USFDA gesture for muscle relaxant infusion

    Zydus Cadila has obtained final acceptance by the US Food and Drug Administration (USFDA) to advertise Cisatracurium Besylate Injection USP at the potency of 20 milligrams (base)/10 mL (two mg/mL) multiple-dose vial, Cadila Healthcare stated in a regulatory filing on Wednesday. The drug will be produced in Liva plant of Cadila Healthcare Ltd.. Zydus Cadila

    India preliminaries for Russia’s ‘Sputnik-V’ antibody may start in next barely any weeks: Dr Reddy’s

    Reddy’s Laboratories Ltd could start late-stage Indian clinical trials of Russia’s potential coronavirus vaccine within the next few months, an executive in the Indian drugmaker said on Tuesday. Indian trials of this Sputnik-V vaccine candidate, being developed by Russia’s sovereign wealth fund, will enroll 1,000-2,000 participants and also be conducted at multiple private and government

    FDA endorsed drug ‘Teicoplanin’ discovered more powerful in treating COVID – 19 infection: IIT Delhi research

    Clinically approved drug”Teicoplanin” is a potential therapeutic alternative against COVID-19 and may be ten times more effective than many drugs being currently used, a study by Indian Institute of Technology (IIT), Delhi has found. The research from the institute’s Kusuma School of Biological Science screened an assemblage of 23 approved drugs, which have shown leads

    Rhizen Pharma gets USFDA endorsement for stage one clinical preliminaries for Covid-19 drug

    New Delhi, Dec 2 (PTI) Rhizen Pharmaceuticals, a member firm of Alembic Pharmaceuticals, on Wednesday said it has received approval from the US health regulator to commence phase one clinical trials on retroviral oral drug for the treatment of COVID-19. The Switzerland-based firm, which will be a clinical-stage oncology-focussed biopharmaceutical company, has obtained approval for

    WHO says specialists examining new COVID-19 variant in England

    Myth 1: Mental illnesses are rare | On October 7, the World Health Organization said “close to one billion people globally have a mental disorder”. (Image: Reuters) The World Health Organization is aware of a new variant of COVID-19 that has emerged in Britain, but there is no evidence the strain behaves differently to existing

    Caplin Point Laboratories arm gets USFDA gesture for Neostigmine Methylsulfate Injection

    New Delhi: Caplin Point Laboratories on Thursday said its subsidiary has received approval from the US health regulator for Neostigmine Methylsulfate Injection. Neostigmine Methylsulfate Injection is a cholinesterase inhibitor and is indicated for the reversal of the effects of non-depolariSing neuromuscular blocking agents (NMBAs) after surgery. “Caplin Steriles Ltd (Caplin) has been granted final approval

    Cipla enters into a licensing agreement with MSD to expand access to investigational oral therapeutic drug for COVID-19 treatment

    Mumbai, India; April 28, 2021: Cipla Limited (BSE: 500087; NSE: CIPLA EQ; and hereafter referred to as “Cipla”) today announced that it has signed a non-exclusive licensing agreement with MSD a tradename of Merck & Co., Inc. Kenilworth, NJ., USA for the manufacturing and distribution of Molnupiravir, the investigational oral antiviral drug currently being studied