BioPharma Dive October 1, 2024
BioPharma Dive staff

Over the next three months, the agency could approve a rival to a fast-selling Pfizer heart drug, a much-debated lung cancer medicine and an addition to Vertex’s dominant cystic fibrosis business.

It’s not a well-known disease. But transthyretin amyloidosis cardiomyopathy, a rare condition affecting the heart, has become the target of a major drug development effort.

One medicine, from Pfizer, is approved and two others, from BridgeBio Pharma and Alnylam Pharmaceuticals, have succeeded in late-stage testing. Deciding which offers the greatest benefit has consumed analysts on Wall Street and top experts in the field. At stake is a market worth billions of dollars.

By Thanksgiving, the Food and Drug Administration is expected to decide on approval of BridgeBio’s acoramidis, likely...

Today's Sponsors

LEK
ZeOmega

Today's Sponsor

LEK

 
Topics: FDA, Govt Agencies
Nearly half of FDA-authorized AI tools may provide little benefit
Sanofi and Regeneron Biologic Drug Dupixent Notches a New FDA Approval in COPD
FDA Roundup: Agency Highlights from September 2024
COVID Preventive Drug Should Work Against Circulating Variants, FDA Now Says
FDA Approval of Bristol Myers Drug Makes It the First Novel Schizophrenia Med in Decades

Share This Article