Category: News

  • Interview with Rodrigo Barnes

    Interview with Rodrigo Barnes

    Interview with Rodrigo Barnes

    Tell us a bit about the institution/company/organisations you work for.

    For the last twelve years, I’ve been working at Aridhia (https://aridhia.com), an SME based in Edinburgh and Glasgow specialising in informatics for biomedical research. After working for some years with specialist clinicians in hospitals and clinics with specialised medical data, we found our current focus at the intersection of clinics, universities and the pharmaceutical industry. As the permaculture people say, ‘cultivate the edge’ – it turns out that’s where the interesting things happen. Our Digital Research Environment (DRE) is a service for securely sharing patient and participant data and running state of the art statistics and machine learning in the cloud. Our job is to make it convenient and secure for communities like EPAD and their wider ecosystem.

    What is your current role in EPAD?

    My background is in mathematics (not statistics!) so far my career has been in the software industry, designing information intensive systems – most recently in the scientific domain. As part of Work Package 4 from the start, my role was driving to design the ‘information architecture’. At the time we knew that a project like EPAD LCS would need both the regulatory database (GCP) and an as-yet-undefined analytical database (GXP for Analytics? that could evolve as the scientific and operational needs were better understood. As well as defining processes for bringing data in and making it useful for multiple purposes, we adapted a data model I had developed integrating hospital data.

    More recently, I have been involved in what comes after the IMI EPAD, from various angles, business and informatics. I am excited at the possibility of taking our expertise in international collaboration to the next level.

    How Aridhia is contributing to facilitate and generate EPAD data release?

    We have learned so much from working in EPAD, and one of the most interesting aspects has been to help define a robust data sharing process for the LCS data. Our team worked with the sponsors, industry partners and l’Academie to achieve this and are involved at every stage. Our data team generate the published snapshots of the analytical database, and publish snapshots and metadata. Researchers can discover the data through publications, Internet searches and go through a partially automated process to request access. A semi-automated process streamlines the review and approval of requests. Data is then usually delivered to a private Workspace in the DRE where they can download the open data, collaborate on analysis and also redeposit derived data back to the LCS. Experience of this process is feeding back into our product design so that we can improve the potential for data discovery and reproducibility in science.

    What value do you see in public-private collaboration and networking with related initiatives?

    We took a strategic decision to invest in EPAD – at the time we had little experience of working directly with industry and our offer was not well understood in this domain. The IMI programme created the conditions for us to learn from the EPAD network and has had a very positive impact in developing our business. On a personal level, it has been a rewarding community of colleagues to work with. Three critical factors were the public-private funding, the scale of being European-wide and the pre-competitive agreements on intellectual property. This combination got us started working with the EPAD partners and setup a framework for us to make a wider contribution than we could have otherwise.

    What are the most prominent challenges you see in Alzheimer’s disease research?

    What I say here is not as a scientist or clinician. As a lay person, I can see the absence of disease modifying therapies leaving patients with little hope, and the challenge of making sense of brain health or disease progression over many years. My specialised perspective sees the patchy and evolving data that hampers clinical and scientific solutions, and the difficulties of distributing analytics-based tools to where they are needed. For now, the Aridhia team and I are working on two specific aspects – how to maximise the available data or design more compatible datasets through international collaborations, and how to deliver machine learning and other decision support into the clinic at scale.

     

    by

    in

    Tell us a bit about the institution/company/organisations you work for. For the last twelve years, I’ve been working at Aridhia (https://aridhia.com), an SME based in Edinburgh and Glasgow specialising in informatics for biomedical research. After working for some years with specialist clinicians in hospitals and clinics with specialised medical data, we found our current focus…

  • COVID-19 Update and online resources

    COVID-19 Update and online resources

    COVID-19 Update and online resources

    The worldwide COVID-19 pandemic has inevitably impacted EPAD and its consortium members. The EPAD project management team is monitoring the situation closely. Most EPAD research and clinical trial activities had to stop as of early March as progressively universities across Europe closed, and the clinical sites were either closed or saw site staff redeployed to help fight this pandemic.

    COVID-19: Sharing experiences and advices from EPAD member José Luis Molinuevo

    “All participants from our observational studies, like EPAD, AMYPAD, ALFA+ study, etc., and trials, PENSA, AB1601, are not allowed, by law, to come in, hence from a safety perspective we are on good grounds. We are aware of the impact on our studies, so we are working hard adapting them with the necessary protocol amendments to ensure their viability and validity after the crisis. Our IT teams are working on existing data to clean it and make it accessible to our research team, who is focusing on analysis and writing results from their homes”, says Dr José Luis Molinuevo, scientific director of the Alzheimer’s Prevention Program at BBRC.

    Moreover, Molinuevo has been part of a correspondence letter in The Lancet, together with Alzheimer’s Disease International (ADI) and experts in the field of dementia. They suggested several measures for people living with dementia, as they are particularly vulnerable to the COVID-19 pandemic.

    He has also published, together with ADI, a position paper on COVID-19 and dementia, with the aim to help families consider key issues when planning care for their loved ones with dementia during this pandemic.

    How COVID-19 has affected the dementia research at the Center of Dementia Prevention in Edinburgh?

    “When COVID-19 arrived in the UK, and with an impending lockdown looming, our sponsor office announced the suspension of all study activity. This means all of our ongoing studies with face-to-face visits have been temporarily halted and we have transitioned the team to work from home. However, the Centre for Dementia Prevention team at the University of Edinburgh always rise to a challenge and although we are missing our participant visits, we’ve been able to creatively continue our work from our home offices. Before lockdown we were looking forward to launching a study looking at public opinions on data sharing in health care research. Initially this was planned as a face to face series of workshops, but we have redesigned the programme to run online. We also have lots of exciting data to look at and ask important research questions of- even though we cannot complete face to face visits with our participants, their data is still contributing hugely to dementia research during this time. We’ve also been able to spend some time on some fun communications projects during this time- we had some micromodules included in the Edinburgh International Science Festival and are working on a website relaunch as a portal to communicate our research work to the public. We are really looking forward to being back in the office soon, but COVID19 won’t stop our efforts to understand more about how we can prevent dementia”, shared Sarah Gregory (EPAD Study Coordinator), Clare Dolan (Research Assistant) and Hannah Pullen (Assistant Psychologist).

    Mercè Boada, Principal Investigator of the EPAD project at Fundació ACE (Barcelona), shares her experiences of COVID-19 lockdown

    At Fundació ACE, they are using telemedicine to perform follow-up on the patients and research participants. Supported by their younger family members, the patients are able to use the telemedicine services to attend consultations and obtain information about their care. The team of social workers provides emotional support and helps people complete the paperwork required to obtain support from the local authorities. The team is also experiencing ethical challenges related to the continuation of the clinical trials, which have been suspended. This was a very difficult decision to make, but they had to consider that the participant population is vulnerable and at high risk of COVID-19 morbidity and mortality. So far, they have suspended their activities and have established the logistics for new possible scenarios in the short and long term.

    Alzheimer Europe has launched a website section with key resources and rung the alarm about discriminatory practices in intensive care settings during the COVID-19 pandemic

    In order to support people with dementia, carers, care professionals and national Alzheimer’s associations during the ongoing COVID-19 situation, our partner Alzheimer Europe has put together a range of valuable online resources with helpful information, tips and guidelines. Ten categories have been published including 1) information for people with dementia; 2) advice for caregivers and family members; 3) information for minority ethnic groups; 4) COVID-19 and intellectual disabilities, 5) Mental health resources; 6) COVID-19 in numbers: epidemiology; 7) Global resources; 8) EU resources; 9) National country resources and 10) General, scientific and ethical resources. These can be found here.

    During these challenging times, there are a number of accurate and up-to-date information on the coronavirus outbreak and the long list of resources that have been gathered shows the invaluable work provided by national Alzheimer’s associations, pharmaceutical companies and government agencies during the COVID-19 pandemic.

    In addition, Alzheimer Europe has rung the alarm about discriminatory practices in intensive care settings during the COVID-19 pandemic. The full position of Alzheimer Europe is online here. On 14 April 2020, the Alzheimer Europe Board adopted recommendations for Alzheimer associations, health and social care professionals on how to promote the wellbeing of people with dementia and carers during the COVID-19 pandemic. For the development of its recommendations, the Alzheimer Europe Board built on in-depth discussions with its member organisations and ministry officials from the European Governmental Expert Group on Dementia who shared some of the innovative ways in which associations and governments continue to provide support to people with dementia. The full recommendations adopted by the Alzheimer Europe Board are online here.

    Jean Georges, Executive Director of Alzheimer Europe commented: “I am in awe at how quickly Alzheimer associations and health and social care professionals have responded to the COVID-19 challenge and continue to provide essential information, support and care to people with dementia and their carers. They deserve the full support of national governments and I hope our recommendations provide some guidance on how to promote the wellbeing of people with dementia and carers in these difficult times.”

    Some additional useful resources:

    by

    in

    The worldwide COVID-19 pandemic has inevitably impacted EPAD and its consortium members. The EPAD project management team is monitoring the situation closely. Most EPAD research and clinical trial activities had to stop as of early March as progressively universities across Europe closed, and the clinical sites were either closed or saw site staff redeployed to…

  • Interview with Jean Manson

    Interview with Jean Manson

    Interview with Jean Manson

    What is your current role in EPAD?

    My current role in EPAD is the PI of the EPAD Bioresource. This is the sample collection that has been taken from EPAD participants from across Europe and is held at the University of Edinburgh. The Bioresource is responsible for the safe storage of these samples and for sending these samples out for analysis. I am also the chair of the Sample Access Committee which reviews all the requests for the use of these samples from both industry and academia. We aim to ensure that this precious collection of samples is put to the very best use towards the prevention of Alzheimer’s dementia.

    What did you do prior to joining EPAD?

    I am a basic scientist and have worked in many areas of research throughout my career including Cystic Fibrosis, transposable elements in maize and Rheumatoid Arthritis but my most recent research was conducted on Prion diseases. I have worked on these diseases for over 30 years throughout the BSE and vCJD epidemics both as a basic scientist and advisor on government and scientific committees. It was a challenging period when we were never far from the attention of the press and public as well as the scientific communities. The Prion diseases are diseases of a misfolded protein in the brain and other tissues and lately my research interest has spread into the other diseases of protein misfolding including Alzheimer’s disease.  Although different proteins are involved in these diseases there are many commonalities in mechanisms in the brain underlying the early events of these different diseases. My research aimed to understand these early events and how to prevent the neurodegenerative outcome and subsequent clinical disease.

    Tell us a bit about the institution/company/organisation you work for.

    I work in different locations of the University of Edinburgh.  Partly at the Centre for Dementia Prevention of the University of Edinburgh where an enthusiastic and multidisciplinary group are all dedicated to the aim of preventing dementia. The Bioresource team is located in a different part of the University. A small and very dedicated team are located at the Roslin Institute where we also get valuable support and assistance from Roslin staff. It is a pleasure and a privilege to work with both centres.

    by

    in

    What is your current role in EPAD? My current role in EPAD is the PI of the EPAD Bioresource. This is the sample collection that has been taken from EPAD participants from across Europe and is held at the University of Edinburgh. The Bioresource is responsible for the safe storage of these samples and for…

  • Two EPAD Fellows successfully defended their PhD thesis

    Two EPAD Fellows successfully defended their PhD thesis

    Two EPAD Fellows successfully defended their PhD thesis

    The EPAD consortium wishes to congratulate Lisa Vermunt and Lucy Stirland, two EPAD fellows, on successfully defending their PhD thesis in March 2020. It was two great days and we are proud of their contributions and all the hard work that Lisa and Lucy have put in – very well deserved! We wish them both the best in their future endeavours! Here is a chance to get to know them and their work a bit better.

    On 13 March 2020, Lisa Vermunt successfully defended her PhD thesis entitled “Secondary prevention for Alzheimer disease – timing, selection and endpoint of clinical trials” at the VU University in Amsterdam (Netherlands). This work was conducted in the context of the EPAD project and was the first EPAD PhD to be completed including EPAD content. Lisa was supervised by Prof Philip Scheltens, Pieter Jelle Visser and Betty Tijms. In this thesis, Lisa investigated the duration of the Alzheimer’s disease stages. As a second independent project, she studied the prognosis of those reverting from mild cognitive impairment. Within EPAD, she studied the recruitment of individuals without dementia for dementia prevention research. Finally, she visited Washington University in St. Louis (US) to study brain connectivity in the DIAN cohort, which consists of families in which autosomal dominantly inherited Alzheimer’s disease occurs. The findings in this thesis improve the insight in the disease course of Alzheimer’s disease, including the pre-dementia period. The findings provide new prognostic information, and can be applied to improve the design and facilitate the execution of secondary prevention trials in Alzheimer’s disease. The published parts of the thesis can be found here.

    Lucy Stirland defended her thesis on 16 March 2020 at the University of Edinburgh (UK). Her thesis is titled “Epidemiology of multimorbidity and polypharmacy in ageing: a complementary analysis of mental and brain health in three datasets”. Her thesis was supervised by Graciela Muniz Terrera, Tom Russ and Prof Craig Ritchie. Her thesis focused on the mental and brain health of people with multiple physical conditions. Most people with one long-term condition have more than one illness, so it’s important to study combinations of diseases. Lucy looked at data from three sources: EPAD, the PREVENT Dementia study and routinely collected data from the Scottish National Health Service. A chapter in this thesis was based on the EPAD V500.0 analysis and has been published already and is available here. The full text of her thesis will shortly be available. Her PhD was funded by the Medical Research Foundation and Medical Research Council through PsySTAR, the Psychiatry: Scottish Training in Academic Research programme.

    EPAD involves many academic, industry and SME partners. What has been your experience as a young researcher of working on such a large public-private partnership?

    • Lisa: I consider it to be a uniquely wonderful experience to have been able to work with a diverse group of experts in Alzheimer research. Naturally I was aware of what I was jumping into, but of course I could not anticipate what the job would be like. EPAD researchers have literally expertise on every detail, from project management to biomarkers. Although, I am sincerely disappointed that the EPAD Cohort cannot continue anymore, I am convinced that all study sites will remain sufficiently creative to keep following the participants over time. Also on a cultural level I have learned a lot about Europe – and all the nuances of the different cultures. I could really recommend it to all starting researchers!
    • Lucy: During my PhD, I gained experience in analysing data from different research studies. It was great to use information collected from the EPAD Cohort Study because there were so many different measurements taken. I was very fortunate that my primary PhD supervisor, Dr Graciela Muniz Terrera, co-leads the EPAD WP2 Work Package “Statistical/Methodology” so she was always on hand to provide guidance. I also enjoyed working with other members of the team who shared their knowledge with me.

    What were your main tasks within the EPAD project?

    • Lisa: As member of Work Package 3, our main responsibilities were to set up and maintain the EPAD Register. My work entailed a lot of reaching out to all the project partners. A second task was to set up the Amsterdam study site and work as site coordinator and the physician for the Cohort study. As I became more focused on writing and data analysis, most EPAD Cohort tasks were assigned to be carried on by other colleagues. It has been nice to see the participants during study visits as a study physician and chat with them about their motivations, their lives, and experience in the project.

    What have been some of your major research findings?

    • Lisa: One of the most important developments, I believe, has been that we made a model that improved on previous models estimating the duration of the clinical Alzheimer’s disease stages. Another really interesting part was that we could confirm that grey matter connectivity is changed in autosomal dominant Alzheimer’s disease in a similar way as in sporadic Alzheimer’s disease. In addition, decline of these connectivity measures worsened as the disease progressed over time, which provides an important validation for this imaging marker of disease progression in Alzheimer’s disease.
    • Lucy: I found links between having several conditions and having depression. In the EPAD cohort, I found that the more conditions people had, the less likely they were to have a positive result for amyloid, a test that suggests higher risk of dementia. This was surprising as we know that people with dementia usually have several other diagnoses. I concluded that the interaction between multiple conditions and dementia was likely due to lots of reasons rather than amyloid alone.

    You recently finished your PhD. Which career track are you pursuing at the moment?

    • Lisa: I am continuing my scientific career with a postdoc position, started a few months ago in the lab of prof. Teunissen of neurochemistry at Amsterdam UMC in the Netherlands. Here I will continue to work on disease modelling, including proteomic data now as well. With this approach we wish to find new prognostic markers and better understand the disease. Apart from that, I am maintaining physician tasks, seeing participants and patients in our Alzheimer center on a regular basis. My plan is to stay in Alzheimer’s disease research at least until we found an effective treatment for the secondary prevention dementia due to Alzheimer’s disease.
    • Lucy: I am an old age psychiatrist and have returned to full-time clinical work since finishing my PhD. I currently work in liaison psychiatry, caring for patients’ mental health while they are in hospital with physical illnesses. Longer term, I aim to pursue a clinical academic career, splitting my time between research and clinical work.

    by

    in ,

    The EPAD consortium wishes to congratulate Lisa Vermunt and Lucy Stirland, two EPAD fellows, on successfully defending their PhD thesis in March 2020. It was two great days and we are proud of their contributions and all the hard work that Lisa and Lucy have put in – very well deserved! We wish them both…

  • Message from the EPAD Coordinators to all involved in the EPAD Longitudinal Cohort Study

    Message from the EPAD Coordinators to all involved in the EPAD Longitudinal Cohort Study

    Message from the EPAD Coordinators to all involved in the EPAD Longitudinal Cohort Study

    A message from the EPAD Coordinators to all involved in the EPAD Longitudinal Cohort Study 

    By now you will all be aware of the unexpected closure of the EPAD Longitudinal Cohort Study. We are writing to you to explain the background to this and also to thank you for your commitment to this research and the fight to understand Alzheimer’s disease better and develop better treatments that will prevent dementia.

    The grant which has funded EPAD from 2015 runs out in June 2020. This grant came from the European Union through the Innovative Medicines Initiative which was set up to allow private companies to work hand in hand with the academic and (where relevant) charitable sector. Since summer 2019, we have been working hard to secure funding for several elements of the EPAD Programme which included the Longitudinal Cohort Study. Unfortunately, our endeavours proved unsuccessful and we were not able to secure the necessary funding which forced us to close the study to our greatest regret.

    As a result, it will no longer be possible to run the Longitudinal Cohort Study as a single study across all of Europe but through the passion and determination of the Principal Investigators and site staff across Europe, research into Alzheimer’s disease will continue. The Principal Investigators in EPAD may find alternative resources either for their own site or at a national level to continue some form of follow up or identify other ways of keeping research participants involved in Alzheimer’s research, if they so wish.

    We know that the research teams will be planning to communicate this with all of the research participants and their study partners in the weeks and months ahead. Clearly the whole world has been affected by the Covid 19 Pandemic – so some of these discussions may be delayed longer than would have normally been the case.

    We’d both like to thank all of the research participants for their commitment to the study – through the time and effort they have made and those of their friends and family who supported them in their visits.

    We also know that everyone involved will have invested a lot of hope in this huge project to make ground breaking discoveries to change the future. The data we have collected already will still be able to achieve this and the longer term follow up that is hoped to be in place will only add to the incredible contribution you have each made individually and collectively.

    On behalf of the entire EPAD consortium and indeed the broad research community globally we cannot thank you enough.

    Thank you and be safe.

    Serge and Craig

    Serge Van Der Geyten is the coordinator of EPAD working at Janssen in Belgium and Craig Ritchie is the coordinator of EPAD working at The University of Edinburgh in Scotland. They have led this programme since its inception in 2014 through the funding becoming available in 2015 to start the programme.

    by

    in

    A message from the EPAD Coordinators to all involved in the EPAD Longitudinal Cohort Study  By now you will all be aware of the unexpected closure of the EPAD Longitudinal Cohort Study. We are writing to you to explain the background to this and also to thank you for your commitment to this research and the…

  • Interview with Graciela Muniz Terrera

    Interview with Graciela Muniz Terrera

    Interview with Graciela Muniz Terrera

    What is your current role in EPAD?
    I co-lead WP2 (Statistical/Methodology Engine Room) and I am also a member of the Balancing Committee that has important input in the selection of individuals into the EPAD Longitudinal Cohort Study. I have been involved in different roles in various publications using the EPAD data.

    Tell us a bit about the institution/company/organisation you work for.
    I work at the Edinburgh Dementia Prevention group of the University of Edinburgh, where I am a senior lecturer in biostatistics and dementia. We are a very active group leading research in dementia prevention, the epidemiology of dementia and ageing and collaborate with numerous local, national and international groups involved in research in these areas. We are leading research in brain health and importantly, we run multiple dissemination activities in Edinburgh and across Scotland.
    We also have several PhD students and early career researchers working with us who are also part of the EPAD academy.

    What are your expectations from the EPAD project?
    EPAD is an outstanding resource for advancing dementia research, filling in important gaps in the field. From an analytical perspective, EPAD provides fantastic opportunities for the application and development of new methodologies to answer substantive questions in dementia that have not been fully answered yet due to limitations in existing data. The fact that the data is open to the wider community is also a plus to maximise its use and enhance opportunities for faster advancements.

    by

    in

    What is your current role in EPAD? I co-lead WP2 (Statistical/Methodology Engine Room) and I am also a member of the Balancing Committee that has important input in the selection of individuals into the EPAD Longitudinal Cohort Study. I have been involved in different roles in various publications using the EPAD data. Tell us a…

  • Interview with Martin Dvorak

    Interview with Martin Dvorak

    Interview with Martin Dvorak

    What is your current role in EPAD?

    I work as a clinical lead at IQVIA where I manage the clinical research associates (CRAs) across all the countries that contribute to EPAD. I provide clinical trial expertise in accordance with protocols and with ICH GCP (International Conference on Harmonisation Good Clinical Practice). As clinical lead, I provide leadership to the clinical team, support the Project Leader, and, in collaboration with the other functional teams from IQVIA, work to meet the project’s overall objectives while optimising quality and timeliness in accordance with our policies and practices. I am focused on the delivery and quality within a project and work to maximise the efficiency of clinical operations and therapeutic expertise, along with diverse IQVIA solutions, to drive operational excellence especially in patient recruitment and on-time high quality data collection.

    What did you do prior to joining EPAD?

    I’ve worked for IQVIA, through legacy Quintiles, since May 2012. I started as a CRA in the Czech Republic and after gaining valuable monitoring experience was promoted to clinical lead in November 2016. I have worked on multiple studies in various therapeutic areas.  I have a Master’s degree in Biochemistry with a thesis on preparation of recombinant cytochrome P450 1A1. I enjoy working in this challenging field and advancing the development of new drugs and diagnosis methods for patients. If we can save even one human life, it is worth it!

    Tell us a bit about the institution/company/organisation you work for

    IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions and contract research services to the life sciences industry. Formed through the merger of IMS Health and Quintiles, IQVIA applies human data science — leveraging the analytic rigor and clarity of data science to the ever-expanding scope of human science — to enable companies to reimagine and develop new approaches to clinical development and commercialization, speed innovation and accelerate improvements in healthcare outcomes. Powered by the IQVIA CORE™, IQVIA delivers unique and actionable insights at the intersection of large-scale analytics, transformative technology and extensive domain expertise, as well as execution capabilities. With approximately 65,000 employees, IQVIA conducts operations in more than 100 countries.

    What are your expectations from the EPAD project?

    EPAD is tremendous project which will bring more clarity into development of Alzheimer’s dementia. It is my honour to work with the trial delivery centres involved in EPAD and with the researchers who contribute their data to the longitudinal cohort study. Hopefully these data will provide additional information about this disease and, more importantly, will provide insights on potential treatment routes for Alzheimer’s dementia. I am confident that EPAD has a bright future and I am so delighted to be part of it.

    by

    in

    What is your current role in EPAD? I work as a clinical lead at IQVIA where I manage the clinical research associates (CRAs) across all the countries that contribute to EPAD. I provide clinical trial expertise in accordance with protocols and with ICH GCP (International Conference on Harmonisation Good Clinical Practice). As clinical lead, I…

  • Highlights 2019

    Highlights 2019

    Highlights 2019

    With the beginning of this new year, the EPAD project is celebrating its fifth birthday.

    We are proud to look back at a lot of successful deliveries. We list herein some of our key highlights of the past 12 months.

    Wishing you all an exciting and happy New Year,

    The EPADistas.

    by

    in

    With the beginning of this new year, the EPAD project is celebrating its fifth birthday. We are proud to look back at a lot of successful deliveries. We list herein some of our key highlights of the past 12 months. Wishing you all an exciting and happy New Year, The EPADistas.

  • EPAD passes the mark of 2,000 research participants for its Longitudinal Cohort Study

    EPAD passes the mark of 2,000 research participants for its Longitudinal Cohort Study

    EPAD passes the mark of 2,000 research participants for its Longitudinal Cohort Study

    The members of the EPAD initiative are glad to announce that its Longitudinal Cohort Study has recruited its 2,000th research participant in Sheffield (UK) this 15th January. Congratulations to the EPAD team in Sheffield (pictured).

    “Since we joined the project last year, patients in our area have been enthusiastic about the opportunities offered to them by participating in the EPAD project. As researchers and clinicians with many years of experience of research in Alzheimer’s disease, we have also been very enthusiastic about the possibilities that this programme offers.  Myself and my team have been extremely excited about the endless possibilities for hypothesis testing that such a large number of patients with longitudinal monitoring and deep phenotyping offer to gain insight into the preclinical and prodromal features of Alzheimer’s disease”, said Annalena Venneri (principal investigator of the EPAD project in Sheffield).

    The EPAD Longitudinal Cohort Study started the recruitment on May 2016 and is composed of individuals who do not have dementia and are already participating in different cohort studies and clinics across Europe. Their participation in the project involve standardised tests and follow-up over several years.

    Currently, EPAD has 29 study sites up and running across 9 European countries (i.e. Belgium, France, Greece, Italy, Netherlands, Spain, Switzerland, Sweden and UK). We are pleased that Cliniques Universitaires Saint-Luc (Brussels, Belgium) became the latest addition to the EPAD family and recruited their first research participants.

    EPAD is a Europe-wide collaboration aiming to improve the understanding of the early stages of Alzheimer’s disease. It combines knowledge and expertise from 39 organisations across multiple sectors from academia and industry, bringing together a wealth of experience to its activities and making it the largest ever public-private partnership in Alzheimer’s disease research.

    by

    in

    The members of the EPAD initiative are glad to announce that its Longitudinal Cohort Study has recruited its 2,000th research participant in Sheffield (UK) this 15th January. Congratulations to the EPAD team in Sheffield (pictured). “Since we joined the project last year, patients in our area have been enthusiastic about the opportunities offered to them…

  • EPAD turns five!

    EPAD turns five!

    EPAD turns five!

    Another EPAD year has passed and we are proud to look back at a lot of successful deliveries and established relationships. We are pleased to present some of our key achievements of the past 12 months.

    February

    On 4 February, over 90 representatives of the EPAD project met in Berlin for an investigator meeting. The objective of the meeting was to prepare the new trial delivery centres to put the EPAD Longitudinal Cohort Study (LCS) into action. The day after, EPAD held its PoC (Proof of Concept) Kick Off meetingFor the first time, we gathered 30 sites (active and in set up) working on the project to share experiences, discuss PoC preparations and build core strategies.

    March

    On 7 March, EPAD passes the mark of 1.500 research participants for its Longitudinal Cohort Study.

    April

    Craig Ritchie and one of the EPAD study participants Eileen Penman featured in national UK news to provide comments on the potential impact of Brexit on EU/UK research collaboration and projects such as EPAD in particular. Both Craig and Eileen highlighted the importance of EU wide collaboration and their concerns on the future standing of Scotland in research outside of the EU.

    The EPAD team was delighted and honoured to have been invited at the IMI Projects Communication Event to present EPAD as an example of good practice of communications.

    May

    The EPAD General Assembly Meeting took place in Geneva (Switzerland). In attendance were scientists, researchers, representatives from pharmaceutical companies, patient organisations, SMEs, EPAD study site members, other experts and research participants from across many different countries, who make up the EPAD family (also referred to as “Epadistas”!).

    July

    For the second time, we exhibited the EPAD study via a large EPAD booth in the exhibition area at AAIC (Los Angeles, US). EPAD also had a business suite at the exhibition area where many engaging meetings with potential interventional owners and other world experts on Alzheimer’s disease prevention took place.

    August

    We received the good news from IMI that the EPAD project, originally scheduled to end in December 2019, has been extended for six months until June 2020.

    October

    In October, the EPAD project was presented at the 29th Alzheimer Europe conference held in The Hague (Netherlands) as per NEURONET invitation.

    November

    We officially announced the external release of the first wave of data as part of the EPAD Longitudinal Cohort Study. The baseline dataset from the first 500 research participants (V500.0) is now available for use by academic researchers and institutions worldwide. The related paper entitled “The European Prevention of Alzheimer’s Dementia (EPAD) Longitudinal Cohort Study: Baseline Data Release V500.0” describing the baseline data from the first 500 research participants (V500.0) has been published online on 26 November in the Journal of Prevention of Alzheimer’s disease.

    In addition, the EPAD V1500.0 dataset has internally been released to the EPAD researchers for an embargoed period of 6 months. 

     

    We would like to thank you all for a fruitful EPAD year. EPAD combines knowledge and expertise from 39 European organisations from academia and industry. This public-private partnership in Alzheimer’s disease research is a unique collaborative effort that draws on the talents of experts from across the Alzheimer’s disease research and drug development community. EPAD emphasises the importance of collaboration between the different European sites and partners to assure the sustainability of its project.  Looking forward to continuous good collaboration in 2020. Wishing you all an exciting and happy New Year,

    The EPADistas


    by

    in

    Another EPAD year has passed and we are proud to look back at a lot of successful deliveries and established relationships. We are pleased to present some of our key achievements of the past 12 months. February On 4 February, over 90 representatives of the EPAD project met in Berlin for an investigator meeting. The…