Amanda Heidt

Amanda is an award-winning freelance science journalist and editor covering everything from ecology and the environment to artificial intelligence and the nitty-grittiest cell and molecular biology. You can find her full portfolio and contact information at www.amandaheidt.com, or follow along on Bluesky and LinkedIn.

Successful drugs from Novo Nordisk and Eli Lilly are just the beginning of what one analyst says could be “the largest therapeutic class of drugs that the biopharma industry has ever seen.”
With the potential FDA approval of an MDMA-based therapy for PTSD on the horizon, biopharma stakeholders are eyeing psychedelics with fresh anticipation.
Traditional ideas of what attracts talent have, in many ways been upended, with some locations faring better than others. And what employees look for in a job is still changing.
After a sluggish start to the year, experts expect an uptick in IPO offerings moving into fall, although it’s unlikely 2023 will fully shrug off its slump.
Longitudinal studies that track patients’ experiences can inform and accelerate the drug approval process for rare diseases.
The new partnership involves an initial payout of $75 million and the potential for up to $2.6 billion in milestone funding.
The Centers for Medicare and Medicaid Services released details about the patient registry it will require physicians to use to prescribe Leqembi, should it be approved by the FDA.