ATMP Trial Registry Symposium 29 January 2026 [Registration closed]
Location: UMC Utrecht, Heidelberglaan 100, Utrecht
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Finding clinical trials involving ATMPs are still a challenge in the current clinical trial registries. This symposium is a great opportunity to gain insights and discuss bottlenecks with experts in clinical trial registries. Find detailed information on the program and the overview of the day below.
REGISTRATION IS CLOSED – If you would still like to participate you can send an e-mail to info@dare-nl.nl
Detailed information:
The role of CCMO’s OMON trial registry
The number of clinical trials for ATMPs is increasing and therefore it is important the information can easily be found and accessed. The OMON registry is the clinical trial registry developed by the CCMO which contains all the information on every clinical trial in the Netherlands. Paula Vossebeld and Stan van Belkum from the CCMO will give an overview on how the OMON registry works, the development, and their way of working as compared to other registry systems like CTIS.
JOIN4ATMP database, website and app
JOIN4ATMP is a consortium that brings together all members of the European University Hospital Alliance with the existing EU-funded T2EVOLVE and RESTORE networks, and with active support from industry partners and patient representatives as core partners. Nara Marella & Antonia Muller will present some of the tools they have developed in this project to get an overview of the European centers that develop ATMPs. In addition, they will discuss the results on the survey involving all ATMP centers in Europe. Find and feel free to take the survey here – feedback will be discussed at the symposium.
Patient perspectives on clinical trial registries
Being able to find information on clinical trials is not only important for clinicians and scientists, but also for patients and their representatives. Patient organizations talk with policymakers, hospitals, universities and research institutions in and outside of the Netherlands with the aim to improve patient access and patient lives. Access to clinical trials and the information around it is therefore critical, and in this session Joost Groen will provide his perspective from his own experience. Mara Tihaya will present the input provided by the DARE-NL Patient Advisory Board. This will be an interactive session for patient representatives in the audience to provide their own perspectives, experiences, requirements and recommendations.
Workshop
After the break, a workshop will be held in a computer lecture room. The main goal of this workshop is to navigate the OMON registry and find specific information on clinical trials guided by demonstrator cases. You will be able to perform guided searches, ask questions to the experts and provide immediate feedback. You will also be asked to provide feedback on the OMON registry that the CCMO can use to further develop the tool.
Program:
09:00 – 09:30 | Walk-in
09:30 – 09:40 | Introduction & meeting goals
09:40 – 10:40 | Paula Vossebeld & Stan van Belkum: Challenges and detailed insights into the OMON registry
10:40 – 11:00 | Break
11:00 – 11:30 | Nara Marella & Antonia Muller: JOIN4ATMP database, website and app
11:30 – 12:00 | Mara Tihaya & Joost Groen: Patient perspective on clinical trial registries
12:00 – 13:00 | Lunch
13:00 – 14:30 | Workshop: exploring the OMON trial registry



