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EU-PEARL is set to transform the way clinical trials are conducted by developing tools and methodologies to create Integrated Research Platforms (IRPs). This novel approach has the potential to make drug development processes more efficient and faster. A pivotal element is the master protocol, which is still a relatively novel concept. Its implications in critical...
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At the recent stakeholder workshop, it was clear that EU-PEARL is focussed on ensuring the clinical trials of the future are going to be fit for purpose for all stakeholders to draw robust conclusions from them. This is an exciting time to be involved in clinical trial design; understanding what the benefits and risks of...
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Courtney is a Trial Manager in the Stress, Psychiatry and Immunology (SPI) Lab at the IOPPN, Kings College London. What drew you to psychiatric research? I grew up in a time where the importance of mental health was on the raise. Besides, I had a genuine desire to help people. And what better way to...
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The context of emergency generated by COVID-19 has not held back EU-PEARL’s Consortium in advancing towards the new paradigm of clinical trials. In fact, this pandemic has highlighted the need to develop a novel framework in the field of clinical research that can facilitate a more agile response to global health challenges. This was the focus of the keynote...
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This past November marked the first 12 months of EU-PEARL. A fruitful time in which the project Consortium has largely focused on laying the foundations to start developing the innovative IRP framework. Once in place, this new paradigm which deepens into the adaptive platform trials approach, will bring more efficacy and speed to the drug...
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Creating a collaborative environment integrated by a diversity of stakeholders is vital to move forward on the innovative paradigm of Integrated Research Platforms (IRPs). Next October, experts from health authorities, ethic committees, patient organizations, health technology assessments, industry/pharmaceutical companies and academic investigators/hospital networks involved in drug development are called to attend EU-PEARL’s first Stakeholder Workshop...
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Around 300 Consortium members are called to attend EU-PEARL second General Assembly Meeting (GAM) organised along four half-day sessions during September and October. All sessions will take place online due to the restrictions imposed by COVID-19. Besides, representing an excellent opportunity to keep the full Consortium abreast of the latest developments in the project, this...
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Key note by Francesco Patalano (Novartis) and Daniel Prieto-Alhambra (University of Oxford). Albeit our different perspectives, we, public and private partners in EU-PEARL share a common responsibility towards society: to improve health outcomes for patients by promoting innovative and more efficient methodologies that enable the timely development of new medicines. Now, the COVID-19 global emergency...
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I work as a marketing and sales director for a large hospitality company and have moved countries often. As the daughter of a French diplomat, I spent many years abroad -I was born in New Caledonia- and later in life, I settled temporarily in Costa Rica, where both my kids where born. There, we enjoyed...
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The domain of EU-PEARL’s research, Integrated Research Platforms (IRPs) and platform trials is relatively new and consequently the vocabulary is still work in progress.  Hence, the need to develop a common understanding and usage of terminology beyond EU-PEARL. With this goal in mind, D2.1. Report on Terminology, References and Scenarios for Platform Trials and Master...
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