Weekend update

David Ermer–Congress, Medical / Rx research, No Surprises Act, U.S. Healthcare–
Photo by Dane Deaner on Unsplash

Happy Labor Day!

From Washington, DC,

  • The Hill reminds us that Congress will return to Capitol Hill for on September 9 for “a three-week sprint, during which lawmakers will face key legislative deadlines and work to push their political messages before departing again for campaign season.”
  • Federal New Network points out,
    • “OMB issued its annual Circular A-11 update in late July and the 1,079-page tome is filled with dates and instructions for how agencies should put the final touches on their 2026 budget requests.
    • “Digging deeper into the primer, agencies will find an extensive treatise on everything from improving customer experience to managing federal real property to updated requirements for using evidence and evaluation in programs. * * *
    • OMB told agencies to prepare for a 3% civilian pay raise as part of their 2026 budget planning.
  • September is the month that OPM announces the next year’s FEHB maximum government contribution and FEHB plans can start sharing their premium news publicly. Back in the day, the announcement was known as the Labor Day press release. However, the announcement has slipped over the past 40 years to the end of the month. With the big Postal Service Health Benefits Program launch set for January 1, OPM may make the announcement earlier in September 2024. It will be interesting to see how FEHB and PSHB premiums compare to one another.
  • Bloomberg has an article about an 11th Circuit No Surprises Act case worth noting.  This air ambulance claim dispute case involves a situation where the IDR arbitrator ruled in favor of the insurer, Kaiser Permanente, and the provider has challenged the arbitration award in federal court. The provider lost at the district court level and has appealed to the 11th Circuit. Here are links to KP’s appellee brief and AHIP’s amicus brief. 

From the public health and medical research front,

  • Per a National Institutes of Health press release,
    • “Research supported by the National Institutes of Health (NIH) has found that measuring two types of fat in the bloodstream along with C-reactive protein (CRP), a marker of inflammation, can predict a woman’s risk for cardiovascular disease decades later. These findings, presented as late-breaking research at the European Society of Cardiology Congress 2024, were published in the New England Journal of Medicine.
    • “We can’t treat what we don’t measure, and we hope these findings move the field closer to identifying even earlier ways to detect and prevent heart disease,” said Paul M. Ridker, M.D., M.P.H., a study author and the director of the Center for Cardiovascular Disease Prevention at Brigham and Women’s Hospital, Boston.”
  • The American Medical Association offers advice on how to encourage communities to control hypertension.
  • Fierce Pharma lets us know,
    • “With the heart failure (HF) patient population rapidly expanding, the timing is right for Bayer’s Kerendia (finerenone). The non-steroidal mineralocorticoid receptor antagonist (MRA) was approved three years ago for chronic kidney disease (CKD) associated with Type 2 diabetes but the bulk of its market potential lies with its ability to treat HF.
    • “Four weeks ago, the company revealed that it had scored a victory in the 3 FINEARTS-HF trial. Now Bayer is putting numbers to the claim, unveiling data from the trial that showed Kerendia reduced the risk of cardiovascular death, as well as well as first and recurrent HF events by 16% compared to placebo in patients with mildly reduced (HFmrEF) or preserved ejection fraction (HFpEF).
    • “Kerendia is the first non-steroidal MRA to meet a primary composite cardiovascular endpoint in a phase 3 trial investigating HF patients with a left ventricle ejection fraction (LVEF) of more than 40%, the company said.
    • “Bayer presented the data at the European Society of Cardiology (ESC) event, Sunday in London. The results also were published Sunday in the New England Journal of Medicine.
    • “It is important to remember that there have been very few medications that have demonstrated a definitive therapeutic benefit for patients with HFmrEF and HFpEF, so we believe these results provide new insights for health care teams and patients alike, especially given the reduction in clinical endpoints like death and hospitalization and improvements in patient-reported symptoms,” Alanna Morris, Bayer’s senior medical director of US Medical Affairs, explained in an email.”
  • The Washington Post and Consumer Reports suggest treatments for sleep apnea other than the CPAP machine.
  • The New York Times reports,
    • “[While] dialysis can prolong the lives of patients with kidney failure, * * * a new study published in the journal Annals of Internal Medicine analyzed data from a simulated trial involving records from more than 20,000 older patients (average age: about 78) in the Veterans Health Administration system. It found that their survival gains were “modest.”
    • How modest? Over three years, older patients with kidney failure who started dialysis right away lived for an average of 770 days — just 77 days longer than those who never started it.
    • “I think people would find that surprising,” said Dr. Manjula Tamura, a nephrologist and researcher at Stanford and a senior author of the study. “They would have expected a greater difference.”
  • The Wall Street Journal notes,
    • “A Sanofi experimental drug for multiple sclerosis delayed disability progression in a late-stage trial, but failed to reduce episodes of new or worsening symptoms compared to an existing treatment in other clinical studies.
    • “The French pharmaceutical company said Monday that results of the clinical trials for tolebrutinib, a drug candidate taken orally and being evaluated as a treatment of various forms of multiple sclerosis, will pave the way for discussions with regulators about potentially bringing the drug to market.
    • “Sanofi’s multiple sclerosis drug Aubagio lost patent protection in key markets last year and the company has been working on a new class of drugs to treat the neurodegenerative disease, which results in accumulation of irreversible disabilities over time. Sanofi sees disability accumulation as a significant unmet medical need for patients with the disease. * * *
    • “The company said the drug met the primary goal of a phase 3 trial by delaying disability progression in patients with non-relapsing secondary progressive multiple sclerosis, a type of the disease in which patients have stopped experiencing confirmed relapses—episodes of new or worsening symptoms—but their disability continues to increase over time.”