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Saturday, July 19th, 2025

    Biotech

  • Fresh off Enhertu success, AstraZeneca and Daiichi claim progress for next cancer drug

    Biotech | Aug 9, 2022

    Fresh off Enhertu success, AstraZeneca and Daiichi claim progress for next cancer drug

    A treatment that AstraZeneca acquired for up to $6 billion in 2020 is showing early promise as a combination agent in lung cancer, where it’s being tested alongside Merck & Co.’s Keytruda.

  • Samantha Truex on biotech hiring, competing for funding and Upstream’s next steps

    Biotech | Aug 9, 2022

    Samantha Truex on biotech hiring, competing for funding and Upstream’s next steps

    The CEO recently led Upstream through a $200 million financing that will support development of an inflammatory disease drug. “We have what investors probably want at this time,” she told BioPharma Dive.

  • Lilly criticizes Indiana abortion law, indicating it may look elsewhere to hire

    Biotech | Aug 8, 2022

    Lilly criticizes Indiana abortion law, indicating it may look elsewhere to hire

    After Indiana’s governor signed a near-total abortion ban into law, the drugmaker said it will rethink future hiring in the state.

  • Senate passage of drug pricing bill brings major defeat closer for pharma industry

    Biotech | Aug 8, 2022

    Senate passage of drug pricing bill brings major defeat closer for pharma industry

    The legislation, which would allow Medicare to negotiate prices on up to 60 drugs by 2029, passed on a party-line vote and now goes to the House, where it is expected to pass.

  • Amgen data on KRAS cancer drug disappoints, opening door for rival Mirati

    Biotech | Aug 8, 2022

    Amgen data on KRAS cancer drug disappoints, opening door for rival Mirati

    Highly anticipated trial results for Lumakras combinations with immunotherapy fell short of expectations, showing significant liver toxicity that limited dosing.

  • Karuna shares soar on schizophrenia drug results

    Biotech | Aug 8, 2022

    Karuna shares soar on schizophrenia drug results

    The company plans to ask regulators to approve its KarXT therapy based on the results, which one analyst called “as good as one could hope for.”

  • Pfizer buys sickle cell drugmaker Global Blood for $5.4B

    Biotech | Aug 8, 2022

    Pfizer buys sickle cell drugmaker Global Blood for $5.4B

    The acquisition gives Pfizer access to Oxbryta, an approved drug for the blood condition, as well as two experimental medicines.

  • How a small UK biotech ended up in Gilead’s hands

    Biotech | Aug 5, 2022

    How a small UK biotech ended up in Gilead’s hands

    MiroBio, which was spun out of the University of Oxford three years ago, drew Gilead’s interest with its autoimmune disease research.

  • FDA approves AstraZeneca, Daiichi drug in breast cancer first

    Biotech | Aug 5, 2022

    FDA approves AstraZeneca, Daiichi drug in breast cancer first

    Enhertu is the first targeted treatment cleared for breast cancers that are ‘HER2 low,’ a new classification that could change how doctors treat the disease.

  • Acadia turned back by FDA on second attempt to get psychosis drug approved

    Biotech | Aug 5, 2022

    Acadia turned back by FDA on second attempt to get psychosis drug approved

    The agency issued Acadia a complete response letter for pimavanserin, for which the company had sought to win an expanded clearance in Alzheimer’s disease psychosis.

  • Lilly takes long view on Alzheimer’s drug as FDA starts expedited review

    Biotech | Aug 5, 2022

    Lilly takes long view on Alzheimer’s drug as FDA starts expedited review

    The pharma said Thursday the FDA had accepted its application for donanemab, starting a six month evaluation for potential accelerated approval.

  • US declares monkeypox a federal public health emergency

    Biotech | Aug 4, 2022

    US declares monkeypox a federal public health emergency

    “We're prepared to take our response to the next level in addressing this virus, and we urge every American to take monkeypox seriously,” HHS Secretary Xavier Becerra said Thursday.

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