Forbes June 10, 2024
Robert Hart

Topline

A panel of experts advising the Food and Drug Administration could on Monday recommend Eli Lilly’s experimental Alzheimer’s drug donanemab for FDA approval, a closely watched decision that could pave the way for the drug to become the second of its kind authorized in the U.S.

Key Facts

What To Watch For

The FDA is not required to follow the recommendations of its expert panels but it does put significant weight in their opinions. It is not clear when the FDA may make a final decision or how long it would take Lilly to roll out the treatment once approved. At least two analysts told Reuters they expect the FDA to eventually approve Lilly’s drug. If approved, the agency...

Today's Sponsors

LEK
ZeOmega

Today's Sponsor

LEK

 
Topics: Biotechnology, FDA, Govt Agencies, Pharma / Biotech
Halozyme Pulls €2B Acquisition Bid as Evotec Commits to Standalone Strategy
More than half of US adults could benefit from GLP-1 medications, researchers find
RNA editing is the next frontier in gene therapy—here's what you need to know
Rand roadblock: Biotech bill’s uncertain future
How Digital Chemistry Will Improve Cross-Functional Collaboration In The Biopharma Industry

Share This Article