26 – 27 April 2021, Amsterdam (NL)

EVENT OUTLINE

This workshop is aimed at all relevant stakeholders in cancer drug development, patients, academic
researchers, regulatory agencies and pharmaceutical companies. It will address the latest
developments in the use of endpoints in cancer drug development. It focuses on the assessment within
the context of other data from clinical trials and looks to define a problem-solving, multi-stakeholder
approach to the future development of endpoints. The workshop will focus on discourse-inducing
presentations and interactive panel discussions.

LEARNING OUTCOMES

• Understanding of past achievements and current challenges in the definition and assessment of endpoints
• Assess the challenges and possible solution in the assessment of time-to-event endpoints
• Updated knowledge on novel endpoints, like measurable residual disease or circulating tumour nucleotides, and possible pathways for validation
• Understanding of strategies to improve the use and overcome obstacles in the use of patient-reported outcomes in cancer drug development
• Develop awareness for the use of endpoints in expedited regulatory pathways.

PROGRAMME COMMITTEE

• Axel Glasmacher (CDDF, DE)
• Ralf Herold (EMA, NL)
• Chitkala Kalidas (Bayer, US)
• Claudia Hey (Merck Healthcare KGaA, DE)
• Denis Lacombe (EORTC, BE)

TARGET AUDIENCE

The target is a multidisciplinary audience of academia representatives, EU and US regulatory bodies (EMA, FDA, National Agencies), pharmaceutical Industry, HTAs and patient advocates.

DRAFT PROGRAMME 

View the draft programme HERE

MEETING DATE

26 – 27 April 2021

MEETING VENUE 

Van der Valk Hotel – Amsterdam Amstel
Joan Muyskenweg 20
1096 CJ, Amsterdam, NL
+31 (0)20 80 01 100
amsterdam@valk.com