Our Experts

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Jayne Hornung

Chief Clinical Officer

Expertise: Biosimilars, GLP-1s, Policy and Regulation, Oncology and Rare Disease, Contracting, Reimbursement and Rebates, Industry Trends, Commercial Strategy, Payer Coverage and Restrictions, Payer Market Research

Jayne Hornung, MMIT’s Chief Clinical Officer, has led the company’s clinical team for the past five years. Jayne maintains a sharp focus on the evolving market access landscape, especially in oncology and complex disease states. In an almost two-decade career with MMIT, Jayne’s research into drug, indication and policy data has helped hundreds of pharmaceutical clients understand market access from a clinical perspective. Prior to joining the company, Jayne worked in various positions across the healthcare and pharma industries, and once owned and operated an independent pharmacy. She graduated as a clinical pharmacist from Philadelphia College of Pharmacy in the late 1990s.

Insights by Jayne Hornung

Article | January 2, 2025

What’s Ahead for Market Access in 2025?

As the pharma industry continues to adjust to the provisions of the Inflation Reduction Act (IRA), the country will soon be ushering in a new presidential administration—leaving the future of the IRA in question.

Article | March 21, 2024

Are We at a Tipping Point for Prescription Digital Therapeutics?

The category of treatments known as ‘digital therapeutics’ is widely misunderstood. Though the term is often conflated with ‘digital health’ tools, such as fitness trackers or meditation apps, digital therapeutics (DTx) are distinguished by their reliance on clinical evidence.

Article | January 4, 2024

What’s Ahead for Market Access in 2024?

While concerns about macro trends like inflation and interest rates are still top of mind for manufacturers, we expect a renewed focus on efficient pipeline performance, portfolio growth, and innovative technology.

Article | September 7, 2023

Spotlight on Vaccines: 2023’s RSV Immunization Approvals

Respiratory syncytial virus (RSV) can impact anyone, but infants and older adults are most at risk of illness. With multiple new immunizing agents gaining FDA approval in 2023—and more in the pipeline—manufacturers and payers have a role to play in educating patients and providers about the importance of immunizations to combat RSV.

Article | June 22, 2023

Navigating the U.S. Patchwork of Biosimilar Laws

The FDA approved the first biosimilar more than eight years ago, and the agency continues to give the green light to multiple agents per year. In fact, 2023 could well be a landmark year in launches, spurred by multiple biosimilars of AbbVie’s Humira (adalimumab) entering the U.S. market.

Article | April 20, 2023

Spotlight on Vaccines: The Inflation Reduction Act’s Impact on Coverage

While the Inflation Reduction Act (IRA) may best be known for mandating Medicare drug price negotiation, the act did much more than that. Among its other accomplishments are the elimination of cost sharing for vaccines under Medicare Part D, as well as improved access to adult vaccines for Medicaid and Children’s Health Insurance Program (CHIP) enrollees.
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