The European Medical Society of Oncology (ESMO) Congress is a must for any oncology professional, with experts from across the globe gathering at the event to discuss all-new trial readouts and promising emerging treatment options.

The conference, which covers everything from solid tumours to haematological malignancies, brings in a wide variety of participants – from biotech and pharma companies to healthcare professionals and investors.

Discover B2B Marketing That Performs

Combine business intelligence and editorial excellence to reach engaged professionals across 36 leading media platforms.

Find out more

At this year’s event, there was no shortage of interesting coverage, with key trial readouts across breast and endometrial cancer, as well as head and neck squamous cell carcinoma (HNSCC) and colorectal malignancies.

In this podcast, the healthcare editorial team catches up with Jack Cuthbertson, senior healthcare analyst at GlobalData, to discuss the highlights from this year’s ESMO 2025 Congress.

Alongside Clinical Trials Arena editor Abigail Beaney and reporter Annabel Kartal-Allen, Jack discusses the most prominent trends observed at the congress, as well as the market impact the notable readouts may have moving forward.

You can download GlobalData’s ESMO 2025 highlights report here

GlobalData Strategic Intelligence

US Tariffs are shifting - will you react or anticipate?

Don’t let policy changes catch you off guard. Stay proactive with real-time data and expert analysis.

By GlobalData

You can also watch the immuno-oncology webinar on-demand here and read further expert commentary from GlobalData’s team here.

Clinical Trials Arena Excellence Awards - Nominations Closed

Nominations are now closed for the Clinical Trials Arena Excellence Awards. A big thanks to all the organisations that entered – your response has been outstanding, showcasing exceptional innovation, leadership, and impact

Excellence in Action
Science 37 has won the Research and Development Award in the Site Innovation category for its FDA inspected Direct-to-Patient Site model, delivering nationwide access, faster enrollment and higher retention. Explore how its virtual-first, in home approach is reshaping trial operations and accelerating time to data-driven decisions..

Discover the Impact