24–26 September 2026 | Hong Kong

The Medicines Patent Pool (MPP) participated in WCC, the World Cancer Congress 2026, and brought its perspective on how voluntary licensing and partnerships can help expand equitable access to cancer medicines in low- and middle-income countries. 

Organised by the Union for International Cancer Control (UICC), the World Cancer Congress brought together cancer organisations, health professionals, policymakers, researchers, advocates and people with lived experience from around the world to exchange knowledge and explore solutions to improve cancer prevention, treatment and care. 

MPP’s participation focused on the role that voluntary licensing can play in expanding access to cancer medicines and supporting broader efforts to improve equitable access to treatment.

MPP Session


Title: From innovation to access – addressing barriers to cancer medicines in low- and middle-income countries
Date & time: Thursday, 24 September 2026, 12:20–13:20 (GMT+8)
Location: Room S228
Convened by MPP
More information on the WCC2026 website

Session overview

How do we ensure that breakthroughs in cancer treatment translate into real access for patients, wherever they live?

That was at the heart of our discussion today at the World Cancer Congress, where we explored how to move from innovation to timely, affordable and sustainable access to cancer medicines in low- and middle-income countries.

Using the public-health voluntary licence for nilotinib as a case study, our all-women panel brought together patient, clinical, civil society and access perspectives:

  • Linda Sitorus, Indonesia CML & GIST Community, brought the reality of patients and families to the centre of the conversation. From delayed diagnosis and long journeys to reach specialists to treatment interruptions and changing generic brands, her experience was a powerful reminder that availability alone is not access, and that where a patient lives should never determine their chance of survival.
  • Giulia Segafredo, Medicines Patent Pool, explained how voluntary licensing can enable multiple manufacturers to produce quality-assured generics, expanding supply and creating competition. The nilotinib experience also shows that signing a licence is only the beginning: partnerships are critical to translate it into medicines reaching patients.
  • Pat Garcia-Gonzalez, The Max Foundation, reinforced that availability must translate to access. Medicines need to be accompanied by diagnostics, reliable supply, patient navigation and solutions to the practical barriers patients face, from transport to continuity of care.
  • Gertrude Nakigudde, Uganda Women’s Cancer Support Organisation (UWOCASO), highlighted the indispensable role of patient and civil-society organisations: providing trusted information, peer support and navigation, addressing language and financial barriers, and ensuring access programmes reflect patients’ real needs.
  • Yehoda Martei, University of Pennsylvania, called for building on established mechanisms such as the World Health Organization Model List of Essential Medicines to identify priorities based on public-health burden and meaningful survival benefit, pointing to immune checkpoint inhibitors as an important potential next frontier.

And throughout the discussion, our moderators Salome Meyer and Stella Bialous, Union for International Cancer Control (UICC), helped bring these perspectives together around a common question: what will it take to build an access model that is sustainable at country level?

The overarching message was clear: we should measure cancer innovation not only by what science can achieve, but by whether that innovation reaches the patients who need it.

Voluntary licensing can be part of the solution. But equitable access ultimately requires quality-assured supply, affordability, diagnostics, sustainable financing, strong health systems, patient engagement and government leadership, all working together.

Innovation matters. Innovation that reaches patients matters even more.

Rapid Fire Session

Abstract Presentation > From Patent to Patients: Early Findings from Voluntary Licensing model for Cancer Medicines through the ATOM Coalition – Giulia Segafredo, MPP

Date and time: Friday 25 September | 14:00 to 15:00 (GMT+8) 

Rapide Fire Stage 1

Connecting with partners at Booth C30

Throughout the conference, MPP welcomed partners and participants at Booth C30 in the exhibition area, to learn more about our work on access to cancer medicines and the role of voluntary licensing in helping make innovative treatments available in low- and middle-income countries.

Join our booth mini-sessions

MPP also hosted a series of short sessions and conversations at booth C30 throughout the Congress.

The MPP Community Advisory Panel in Action
Why do community voices matter for access to medicines? Join CAP members Denise Ejoh, Salomé Meyer and Gertrude Nakigudde as they discuss how their insights and lived experiences contribute to MPP’s strategic thinking and decision-making.

The session was live streamed on YouTube.

MPP Explained: Expanding Access Through Voluntary Licensing (Chinese/English bilingual session)
Curious about MPP’s work? This session, delivered in Chinese, will introduce MPP’s model, explain how voluntary licensing works, and explore how it supports access to innovative medicines in low- and middle-income countries.

The session was live streamed on YouTube.

Meet the MPP Team!

  • Meet Giulia Segafredo, Senior Access Manager, Non-Communicable Diseases (NCDs)
  • Meet Hillary Mutungi, Access Officer
  • Meet Shihan Liu and Sophie Thievenaz, Communications Team

Meet our MPP team at the conference!