In case you missed it, our latest feature takes a deep dive into a very interesting area of drug research: ion channels. These proteins made $VRTX one of the world's wealthiest biotechs. Now others are getting in on the action. #biotech#science#biopharma https://t.co/osZNcjK4xE
Jacob is a masterful storyteller and this feature from last year is a good example.
ASBPE agrees - Jacob's story won National Gold for best feature and anchored a portfolio they judged to be "best body of work by a staff journalist" (announced y'day).
Give it a read!
Extremely proud to say the American Society of Business Publication Editors awarded me Best Body of Work by a Staff Journalist and Best Feature at their national awards ceremony yesterday. @ASBPE
The work is, of course, far from finished. If you have ideas for a story that needs telling, please reach out. Thank you to my BioPharma Dive team, whose support gave me the bandwidth to investigate this topic and write these stories.
Biotech M&A on track to have 2nd most active year in history w/ more early stage deals. Nice summary of which funds have benefited from recent M&A from Stifel @TimOpler $XBI $IBB
This is an incredible ending for a therapy I've followed for years. If you're interested in the backstory, here's a feature from 2020, when the FDA issued an astonishing rejection to Roctavian's approval application. https://t.co/JsGdGZpUb3
BioMarin has chosen to pull its once highly anticipated gene therapy for hemophilia from the market. The therapy struggled commercially, which led $BMRN to search for a potential buyer. In the company's latest earnings, it reveals it couldn't find one.
$NBIX "has the scarcity value of being one of only several biotech companies whose ~$3B in existing commercial revenue is expected to grow by more than 50% by 2030 and be durable well into the next decade," he wrote.
So, Abrahams writes, while $NBIX hasn't often been seen as a takeout target, if this gap continues between where investors vs. analysts value the stock, Neurocrine could certainly be attractive to a large pharma acquirer.
"This is why clear, pragmatic, consistent regulatory guidance is essential. The types of individualized genetic therapies that we're trying to develop simply do not fit in the traditional model of drug development."
Rebecca Ahrens-Nicklas, an attending physician at CHOP and part of Baby KJ's treatment team: "Disease communities face real uphill battles when it comes to developing new therapies." #FDA#HHS
"The biggest hurdle, though, is moving beyond a first in human trial to regulatory approval. Getting past that gap is what allows treatments to become commercially available, reimbursed and scaled so all patients who need them can access them ... "