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Thursday, May 22nd, 2025

    Biotech

  • Beam details reasons for FDA hold on base editing cancer therapy

    Biotech | Aug 31, 2022

    Beam details reasons for FDA hold on base editing cancer therapy

    The regulator has asked Beam for a range of technical data before it can start testing the blood cancer treatment in humans.

  • FDA clears updated COVID-19 boosters from Pfizer, Moderna

    Biotech | Aug 31, 2022

    FDA clears updated COVID-19 boosters from Pfizer, Moderna

    The new shots, which are designed to better target circulating strains of omicron, could be available within days. Advisers to the CDC are set to meet later this week.

  • Pfizer lures first chief marketing officer from Verily

    Biotech | Aug 31, 2022

    Pfizer lures first chief marketing officer from Verily

    Drew Panayiotou led marketing efforts at Alphabet’s life sciences arm Verily, and his appointment is Pfizer’s third senior-level hire this year.

  • Funds for free COVID-19 vaccines could run out as early as January, HHS says

    Biotech | Aug 31, 2022

    Funds for free COVID-19 vaccines could run out as early as January, HHS says

    The commercial market for COVID-19 vaccinations could be similar to that for seasonal flu shots and other vaccines, an official with the department said.

  • Jounce’s latest setback dampens outlook for another cancer immunotherapy target

    Biotech | Aug 30, 2022

    Jounce’s latest setback dampens outlook for another cancer immunotherapy target

    The biotech's drug prospect vopratelimab has become the latest member of a group of medicines targeting a molecule called ICOS to fall short of expectations in clinical testing.  

  • Neurocrine, with latest deal, gets a foothold in Europe

    Biotech | Aug 30, 2022

    Neurocrine, with latest deal, gets a foothold in Europe

    The neuroscience-focused company has agreed to buy U.K.-based Diurnal for around $57 million, a move it expects to “accelerate the establishment of its clinical development and commercial activities” in Europe.

  • Atlas Venture’s Bruce Booth on testing the IPO waters and putting the ‘tech’ in biotech

    Biotech | Aug 29, 2022

    Atlas Venture’s Bruce Booth on testing the IPO waters and putting the ‘tech’ in biotech

    In a wide-ranging conversation with BioPharma Dive, Booth, a prolific builder of new biotechs, said he’s starting to see positive signs for startups considering an IPO or private financing.

  • Akili CEO Martucci sees ‘massive’ need for company’s ADHD video-game treatment

    Biotech | Aug 29, 2022

    Akili CEO Martucci sees ‘massive’ need for company’s ADHD video-game treatment

    With enough cash now to last two years, the company, which merged with a SPAC last week, hopes it can change the way children with ADHD are treated.

  • AstraZeneca, matching Lilly, reports positive heart failure data for diabetes pill

    Biotech | Aug 29, 2022

    AstraZeneca, matching Lilly, reports positive heart failure data for diabetes pill

    The new data position AstraZeneca to significantly expand use of Farxiga in heart failure and compete with Lilly and Boehringer Ingelheim’s rival drug Jardiance. 

  • Bristol Myers, Bayer study results seed doubt about an emerging group of blood thinners

    Biotech | Aug 29, 2022

    Bristol Myers, Bayer study results seed doubt about an emerging group of blood thinners

    Though the companies plan to move their medicines into late-stage testing, they each missed their main Phase 2 goals, raising questions about the prospects of so-called Factor XI inhibitors. 

  • Incyte secures second approval for targeted cancer drug

    Biotech | Aug 29, 2022

    Incyte secures second approval for targeted cancer drug

    Sold as Pemazyre, the drug, which blocks well-known cancer proteins known as FGFRs, is now also cleared for use in certain patients with very rare and aggressive blood cancers.

  • Psychedelic clinical trials: What sponsors should know when designing new protocols

    Biotech | Aug 29, 2022

    Psychedelic clinical trials: What sponsors should know when designing new protocols

    With regulators and lawmakers seemingly on board, sponsors have more opportunities than ever to pursue clinical research in this high-velocity area.

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