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Specialty pharmacies (SPs) play a crucial role in delivering complex medications to patients who require ongoing support throughout their treatment journeys. However, the effectiveness of SPs often hinges on timely intervention, efficiency, and seamless collaboration among stakeholders. These challenges are further amplified by time-consuming manual processes, delayed responses, and lack of real-time visibility into patient […]

Guiding patients through their treatment journey is a critical yet intricate task for patient services teams. One of the biggest obstacles they face is “patient drop-off,” the moments when individuals disengage or discontinue treatment. These drop-offs can significantly impact healthcare outcomes, operational efficiency, and access to care. This blog explores the key stages in the

Macular telangiectasia (MacTel) type 2, a rare neurodegenerative eye condition, has long left many without access to effective treatment. This disease silently affects central vision, making everyday tasks like reading and recognizing faces increasingly challenging for those impacted. However, patients and biopharma professionals alike have reason to look ahead with renewed optimism. On March 6,

Every year, millions of people around the world come together to show support and amplify the voices of those living with rare diseases. Rare Disease Day, observed on February 28 (or 29th on leap years), is a vital opportunity to increase public awareness and understanding of rare diseases, their impact, and the need for more

The treatment landscape for rare diseases is rapidly evolving, offering both opportunities and challenges for biopharma professionals and patient service teams. With over 7,000 known rare diseases affecting an estimated 300 million people globally, the need for innovation and collaboration has never been greater. Yet, rare diseases are often underfunded, understudied, and misunderstood, leaving many

Rare diseases affect approximately 30 million people in the United States, yet the path to diagnosing and treating these conditions remains notoriously complex. With small patient populations, high treatment costs, and the necessity for robust engagement strategies, the rare disease sector is filled with challenges. For biopharma professionals, the focus remains on finding innovative ways

The landscape of rare diseases is evolving rapidly, with groundbreaking cell and gene therapies leading the way. These innovative treatments offer hope to patients with diseases previously considered untreatable. However, with innovation comes complexity—bringing these therapies to market isn’t just about scientific breakthroughs but also navigating unique market access challenges. This blog dives into the

Understanding how data and technology intersect with patient support services is essential for teams striving to improve patient outcomes. At the recent Access Patient Support Services Congress, a panel discussion titled “Optimizing Patient Services — Leveraging Data and Technology to Improve Patient Programs” gathered experienced leaders in patient services to share their valuable insights on

Eli Lilly has consistently demonstrated its dedication to precision oncology, and its latest acquisition is a testament to that commitment. The biopharma giant announced a $2.5 billion deal with Scorpion Therapeutics to acquire an experimental cancer drug targeting PI3Kα mutations. This strategic move positions Lilly to further advance its oncology portfolio and address significant unmet

Market access in the biopharma industry goes beyond delivering innovative therapies—it’s about ensuring patients receive timely and seamless access to those treatments. Two key metrics, fill rate and time-to-fill, have emerged as essential benchmarks for assessing operational efficiency, improving patient access, and aligning with strategic goals. But how can biopharma professionals effectively use these metrics