
Adam Feuerstein
Senior Writer, Biotech at STAT
Biotech reporter @statnews. Dog ❤️er. Polk Award winner. #COYS. Said one analyst: The likes of Adam Feuerstein attack viciously. On Signal: stataf.54
Articles
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2 days ago |
statnews.com | Adam Feuerstein
This is the online version of Adam’s Biotech Scorecard, a subscriber-only newsletter. STAT+ subscribers can sign up here to get it delivered to their inbox. Insmed CEO Will Lewis keeps a newspaper story from 2014 framed on the wall of his office. The headline reads, “Insmed joins the biotech trash heap.”If you’re wondering, I didn’t write that story, although I could have.
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1 week ago |
statnews.com | Adam Feuerstein |Matthew Herper |Jason Mast |Lizzy Lawrence
The ouster of the Food and Drug Administration’s chief regulator of cell and gene therapies earlier this week came immediately after a disagreement with her boss over the review of a cell therapy for Duchenne muscular dystrophy, STAT has learned. The regulator, Nicole Verdun, had scheduled an advisory committee meeting to review the therapy developed by Capricor Therapeutics.
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1 week ago |
flipboard.com | Adam Feuerstein |Matthew Herper |Jason Mast |Lizzy Lawrence
1 hour agoI found the easiest way to delete myself from the internet (and you shouldn't wait to use it, too)If you're looking for a data removal service that can remove you from data broker sales lists and people search websites, Incogni should be on your …5 hours agoYour Apple Watch Is About to Get a Pretty Cool New AbilityApple is gearing up to give your Apple Watch some of your iPhone’s standout features.
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1 week ago |
statnews.com | Elaine Chen |Adam Feuerstein |Allison DeAngelis
Why did the Food and Drug Administration suddenly oust one of its top gene therapy regulators? Is the agency growing too political? And should private firms fund academic research? We chat about all that and more on this on this week’s episode of “The Readout LOUD,” STAT’s biotech podcast. We discuss the tragic news that a second teenage boy with Duchenne muscular dystrophy died after taking Sarepta Therapeutics’ gene therapy, raising renewed questions about the FDA’s standards for approving drugs.
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1 week ago |
statnews.com | Adam Feuerstein
This story is an excerpt from Adam’s Biotech Scorecard, a subscriber-only newsletter. STAT+ subscribers can sign up here to get it delivered to their inbox. Cogent Biosciences and Blueprint Medicines are direct competitors who hate each other. During a talk at the recent Jefferies Global Healthcare Conference, Cogent CEO Andy Robbins said Blueprint Medicines’ Ayvakit was so toxic that it was killing patients.
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By the way, I am 100% supportive of legitimate efforts to streamline the FDA drug review and approval process. I agree that there are redundancies and requirements that should be removed or altered to speed up drug reviews and make them less expensive. But handing out political

Stop with all the bad FDA voucher takes, please. This is a total politicization of the FDA's drug review and approval process. It's pure political patronage, not science. @JMaraganore -- you, of all people, know better. Makary gets to hand out "undesignated" vouchers to

Some brake-tapping perspective in this story on Makary's latest PR adventure. FDA announces a new priority review program in bid to further administration goals https://t.co/Njqp6I3zJR via @LizzyLaw_