
Trump Expected to Nominate White House Adviser for FDA Commissioner
President Trump is expected to nominate Heidi Overton, a White House adviser, to lead the Food and Drug Administration.
Staff reporter at Bench to Bed, covering Medical Research.

President Trump is expected to nominate Heidi Overton, a White House adviser, to lead the Food and Drug Administration.

A former top official at the National Institute of Allergy and Infectious Diseases has pleaded guilty to charges related to concealing records from Freedom of Information Act requests.

A nonprofit group is suing the Trump administration over the process of updating the nation's dietary guidelines, alleging that the government improperly rewrote the guidelines with the help of a 'secret panel' of scientists backed by the beef and dairy industries.

Bon Secours Mercy Health, a nonprofit health system, has earned significant revenue from its minority position in Ensemble Health Partners, a medical billing firm.

Compensation for health care CEOs in Massachusetts has increased, despite challenges faced by hospital systems.

Eyepoint's experimental treatment for age-related blindness fails to meet primary goal, while Amylyx's Avexitide shows promise.

States face a September 30 deadline to decide whether to participate in a federal program offering 'most-favored nation' drug prices for Medicaid. The program aims to reduce costs, but its long-term impact remains uncertain.

Eyepoint's experimental treatment for age-related blindness fails to meet primary goal in Phase 3 clinical trial.

The Internal Revenue Service is investigating UnitedHealth Group for allegedly funneling money through a foreign subsidiary to underpay taxes.

Sanofi, a major pharmaceutical employer in Massachusetts, will lay off 229 workers as a result of its acquisition of Blueprint Medicines.

Epic Systems, the nation's dominant seller of electronic health records software, is facing a series of unprecedented challenges driven by antitrust lawsuits, questions about its artificial intelligence strategy, and an exodus of key technology leaders.

Robert F. Kennedy Jr.'s contrasting views on vaccination and addiction were on display in Washington and Los Angeles.

The Internal Revenue Service is investigating UnitedHealth Group, seeking to increase taxable income from 2017 to 2020, and potentially affecting future years.

AstraZeneca discontinues a late-stage trial for its experimental drug volrustomig, while prescription drug prices in the U.S. experience a significant decline.

The use of wearable devices to track health metrics is being promoted by health insurance companies and the Department of Health and Human Services, but experts are raising concerns about the potential for increased costs and exploitation of personal data.

Commure, a $7 billion health software company, has terminated its customer referral program that offered payments for promoting its AI tools to new medical clinics. The decision follows a STAT investigation into the company's referral arrangements, which were disclosed in internal emails from Chief Legal Officer Dan Brian.

Health Secretary Robert F. Kennedy Jr. recently visited California to discuss changes to addiction treatment, placing blame on the prior administration for handling the issue.

Novo Nordisk's CEO believes investors are underestimating the demand for differentiation among obesity drugs, and that new treatment options like pills will prevent the market from becoming a winner-take-all battle with rival Eli Lilly.

Both the U.S. and U.K. health systems prioritize clinical interventions over community-based prevention, despite rising chronic illness and loneliness. A shift toward social infrastructure and community empowerment could reduce strain on hospitals and improve public health outcomes.

Several pharmaceutical companies have recently made notable appointments and promotions, with Formation Bio hiring a new chief scientific officer and head of research and development.

Luigi Mangione has pleaded guilty to federal stalking charges in the killing of UnitedHealthcare CEO Brian Thompson. Mangione admitted to trailing Thompson to an investor conference and shooting him on a New York City street in 2024.

Valisure accuses USP of making false and misleading remarks about its testing methods, sparking a lawsuit.

The U.S. FDA has approved Bristol Myers Squibb’s oral drug iberdomide, marketed as Zenbexus, for use with daratumumab and dexamethasone in patients with relapsed or refractory multiple myeloma, marking the first approval of a novel drug class for the disease and the inaugural use of a more sensitive remission endpoint in the United States.

The U.S. FDA has approved Zenbexus, Bristol Myers Squibb’s oral treatment for advanced multiple myeloma, introducing a new class of blood cancer drugs known as CELMoDs. Meanwhile, a U.S. appeals court revived a $6.7 billion lawsuit accusing Bristol Myers of delaying regulatory approvals for three drugs post-Celgene acquisition.