Merck’s Lipfendra gains FDA nod as first oral PCSK9 inhibitor

TL;DR Summary
Merck’s cholesterol pill Lipfendra (enlicitide) was approved by the FDA, becoming the first oral PCSK9 inhibitor on the market and offering an alternative to injectable cholesterol drugs. The decision was based on two late‑stage trials showing significant LDL‑C reductions across a broad patient group, including those with familial hypercholesterolemia and statin users. The drug could help Merck diversify beyond Keytruda, with analysts forecasting potential tens of billions in peak sales amid competition from injectable PCSK9 drugs like Repatha and Praluent.
- Merck’s cholesterol pill gets US FDA approval CNN
- The F.D.A. Approves a New Pill to Slash Cholesterol Levels The New York Times
- FDA Approves First-of-Its-Kind Cholesterol Pill, Ushering In New Wave of Treatment WSJ
- Merck’s LIPFENDRA® (enlicitide) is the First and Only Once-Daily Oral PCSK9 Inhibitor Approved by the U.S. FDA to Reduce LDL-C in Adults with Hypercholesterolemia Yahoo! Finance Canada
- Drugmaker Merck announces approval of new cholesterol-fighting drug The Guardian
Reading Insights
Total Reads
0
Unique Readers
2
Time Saved
192 min
vs 193 min read
Condensed
100%
38,491 → 80 words
Want the full story? Read the original article
Read on CNN