
Pharma Pulse: A Win for Bone Health
In today’s Pharma Pulse, the FDA clears new denosumab biosimilars for osteoporosis and cancer-related bone loss, while healthcare leaders grapple with a surge in "nuclear verdicts" driven by shifting public sentiment.
Welcome to Pharma Pulse, a Pharmaceutical Commerce podcast where we bring you the latest insights shaping patient access, supply chain/logistics, data & tech, and healthcare innovation. I’m your host, and let’s get into today’s headlines.
- First, a significant expansion in affordable bone health. The FDA has
approved Boncresa and Oziltus, two denosumab biosimilars developed by Amneal Pharmaceuticals and mAbxience. Boncresa, referencing Prolia, is indicated for osteoporosis in high-risk patients, while Oziltus, referencing Xgeva, targets cancer-related bone loss and the prevention of skeletal-related events. These approvals represent the ninth set of denosumab biosimilars to hit the US market. - Turning to the legal landscape, a
report warns of a troubling shift in medical malpractice. Jurors are increasingly viewing physicians and hospitals as part of a profit-driven "empire" rather than as healers. This shift is fueling a surge in "nuclear verdicts"—jury awards exceeding $10 million. Data shows the average of the top 50 medical malpractice verdicts has spiked from $32 million in 2022 to an alarming $56 million in 2024. Experts point to "social inflation" and "reptile theory" tactics in court, where attorneys frame the healthcare system as a danger to the community, effectively shifting the burden onto providers to prove they prioritize patients over profit.
That’s it for this episode of Pharma Pulse. For more insights on trends transforming pharmaceutical access and care delivery, visit
Thanks for listening—until next time, stay well and stay informed.
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