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Dr Steven Yates Weighs How Relationships Between Nurses, Patients Influence Biosimilar Acceptance
Steven Yates, MD, explains how the relationships that nurses have with patients can influence biosimilar acceptance.
The Center for Biosimilars® interviewed Steven Yates, MD, a medical oncologist and medical director at Intermountain Healthcare in Las Vegas, Nevada. Three years ago, Intermountain hired him to lead its biosimilar adoption effort.
Dr Yates explains how critical nurse navigation is for all aspects of oncology, which can make explaining clinical and symptom information to patients easier. He said that nurses can be a valuable resource for patients for explaining complicated concepts, especially in regard to treatment selection. Yates also discussed his experience with the nurse navigators at his practice and how patients have an easier time contact them than their providers. Nurse navigators can allow for patients to be more in touch and informed on their care needs between office visits. Yates said it's important for patients receiving oncology therapy to be in contact with health care institutions in some capacity and that nurse navigators can also keep providers informed on any issues the patient is experiencing.
How AI Can Help Address Cost-Related Nonadherence to Biologic, Biosimilar Treatment
March 9th 2025Despite saving billions, biosimilars still account for only a small share of the biologics market—what's standing in the way of broader adoption and how can artificial intelligence (AI) help change that?
Will the FTC Be More PBM-Friendly Under a Second Trump Administration?
February 23rd 2025On this episode of Not So Different, we explore the Federal Trade Commission’s (FTC) second interim report on pharmacy benefit managers (PBMs) with Joe Wisniewski from Turquoise Health, discussing key issues like preferential reimbursement, drug pricing transparency, biosimilars, shifting regulations, and how a second Trump administration could reshape PBM practices.
Biosimilar Approvals Streamlined With Advanced Statistics Amidst Differing Regulatory Requirements
February 25th 2025The FDA and European Medicines Agency (EMA) mandate high similarity between biosimilars and reference products, but their regulatory processes differ, especially with multiple reference products.
