
Jacob Bell
Reporter at BioPharma Dive
Dad says I'm not an effective communicator. Senior Reporter @biopharmadive. Formerly @TheStreet, @educationweek, @mcclatchydc.
Articles
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2 weeks ago |
biopharmadive.com | Jacob Bell
GSK is betting potentially billions of dollars that a smaller drug company’s technology can help create new treatments for brain-corroding diseases. Through a licensing deal announced Sunday, GSK has gained access to drug delivery technology from South Korea’s ABL Bio.
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2 weeks ago |
biopharmadive.com | Jacob Bell
The world’s largest pharmaceutical companies mostly steered clear of billion-dollar acquisitions in the early months of this year, perhaps indicating how a tumultuous U.S. political environment has led would-be buyers to view bigger deals as too risky for the time being.
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3 weeks ago |
biopharmadive.com | Jacob Bell
The Food and Drug Administration approved on Friday a new type of medicine for people with the rare bleeding disorder hemophilia. Current hemophilia treatments generally try to replace or spur the production of key blood-clotting proteins that are missing because of genetic mutations. But this newly approved medicine works differently. A snippet of genetic code, it gums up production of that keeps blood cells from sticking together.
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3 weeks ago |
yahoo.com | Jacob Bell
This story was originally published on BioPharma Dive. To receive daily news and insights, subscribe to our free daily BioPharma Dive newsletter. The Food and Drug Administration approved on Friday a new type of medicine for people with the rare bleeding disorder hemophilia. Current hemophilia treatments generally try to replace or spur the production of key blood-clotting proteins that are missing because of genetic mutations. But this newly approved medicine works differently.
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3 weeks ago |
biopharmadive.com | Jacob Bell
Eli Lilly plans to appeal a verdict from key drug regulators who say the company’s new treatment for Alzheimer’s disease should not be cleared for the European market. On Friday, the European Medicines Agency recommended that Lilly’s Kisunla not receive marketing authorization because its benefits don’t outweigh its potential risks.
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RT @BioPharmaDive: Novartis builds case for new SMA gene therapy https://t.co/VisHYKWx7c $NVS by @realJacobBell

RT @BioPharmaDive: Latigo raises $150M to get non-opioid pain drugs through key tests https://t.co/Y7XlAQk6XC by @realJacobBell

RT @NedPagliarulo: $JNJ aticaprant is a kappa opioid antagonist, like $NRMA's navacaprant, which failed in a key study two months ago: htt…