News|Articles|October 30, 2025

Payers Are Bracing for the Specialty Trend of the Future | AMCP Nexus 2025

Author(s)Denise Myshko
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Key Takeaways

  • Specialty drugs, especially biologics, will constitute a significant portion of global drug spending by 2029, driven by cancer care costs.
  • Autoimmune diseases and multiple sclerosis are key short-term drivers, while cell and gene therapies for rare diseases lead long-term trends.
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Prime Therapeutics executives discuss specialty drug trends at AMCP Nexus. Key areas include autoimmune therapies, multiple sclerosis treatments, and emerging cell and gene therapy challenges for payers.

Specialty drugs continue to be at the top of many spending reports, and employers predict healthcare costs will increase about 9% for 2026, according to a recent report from Business Group on Health’s Employer Health Care Strategy Survey. One of the biggest cost drivers is cancer care. For the fourth year in a row, the growing prevalence of cancer diagnoses and escalating costs have led to increased spending.

In the last 20 years, more than 1,000 novel drugs have been launched globally, including almost 400 in the past five years. In the United States in 2024, 48 novel drugs were launched, representing a 22% increase from the 2015 to 2019 period. Specialty biologic drugs are expected to have an impact on spending.

Specialty medicines will represent about 46% of global drug spending by 2029 and 54% in developed markets, according to IQVIA’s most recent Global Use of Medicines report.

“The specialty space will continue to grow. We have seen growth over the past decade, and we will continue to see that trend,” Yuqian Liu, Pharm.D., senior director, specialty clinical solutions at Prime Therapeutics, said in an interview.

Managed care, she said, will be challenged to find the right tools to manage through this innovation and be able to bring them to patients. “There is no way that our healthcare system can keep up with that growth,” Liu said. “It’s up to the managed care professionals to see what we can do through innovation: What additional tools can we utilize to be able to keep the trend down? I don’t anticipate we’ll be able to decrease the trend, but maybe we can slow it down or flatten it.”

Liu and her colleague Soumya Vishwanath, Pharm.D., formulary management director at Prime Therapeutics, spoke with Managed Healthcare Executive before the Academy of Managed Care Pharmacy (AMCP) Nexus meeting, which was held at the Gaylord National Resort and Convention Center in National Harbor, Maryland, outside of Washington.

Below they provide an overview of the specialty market to come.

Q: What are the biggest trends in specialty in the short term and long term?

Liu: According to our forecast, autoimmune multiple sclerosis will continue to be the driver for both medical and pharmacy benefit trends over the course of the next three years. In the long term, cell and gene therapies and rare diseases will likely lead the trend long term. There is a lot of cell and gene therapy in early product development. More than 40% of all the drugs in development are for rare disease indications.

Q: How are payers approaching coverage of autoimmune and MS therapies? What are their strategies?

Liu: Biosimilars are definitely a part of the approach for autoimmune. There is a huge trend in the market to drive toward biosimilar utilization in the autoimmune space. The biosimilar products are first-generation and second-generation biosimilars; they have their unique benefits depending on which product they’re looking at. But these [branded] products continue to be trend drivers in the market, and they hold a substantial amount of utilization.

There’s a fine balance between clinical efficacy and the cost. Managed care has tried to find the balance between the quality of care and the cost. Biosimilars have their rightful place as the most cost-effective agents on the market. They still are efficacious. Maybe the efficacy is not as high as some of these newer agents.

For MS, we see a generics-first strategy. The more expensive agents have better efficacy, and they can be used in a broader patient population. That’s why they still hold a large amount of market share.

Q: How are payers looking at gene therapies?

Vishwanath: Cell and gene therapies are being developed for a lot of rare diseases that don’t have any treatments at the moment. These are really innovative products that are going to be coming to the market.

But payers are facing the growing pressure of managing the complexity of these products. They are looking at balancing the cost and the affordability but also recognizing that a lot of these products have very highly individualized care pathways for our patients and for the ecosystem in general. There is going to be a blending of the traditional management approach with utilization management, but also taking a little bit more of an innovative approach to ensure we have access for our patients.

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