The members of the “conect4children” (c4c) initiative today announced the start of a large collaborative paediatric network that will facilitate the development of new drugs and other therapies for the entire paediatric population in Europe. The conect4children (collaborative network for European clinical trials for children, (c4c)consortium aims to enhance the competitiveness of Europe as a critical region for developing medicines for children by using existing expertise, patient access and developing common processes to be applied to disease natural history studies, registries, studies of new therapies and comparisons of existing therapies.
The consortium is a novel collaboration between academic and private sectors that includes 33 academic and 10 industry partners from 20 European countries, more than 50 third parties and around 500 affiliated partners.
The six-year project, comprised of a multidisciplinary public-private consortium, brings together key stakeholders across academia and industry. It is a pioneering opportunity to build capacity for the management of multinational paediatric clinical trials across Europe whilst ensuring the voices of children, young people and their families are heard. Strong links with regulators will be established.
There are many scientific and operational challenges faced by both pharmaceutical companies and academia when running paediatric clinical trials. According to Prof. Carlo Giaquinto of Fondazione PENTA Onlus and University of Padova, who coordinates the project, “c4c will address critical problems with the design, implementation and operational conduct of paediatric clinical trials, such as fragmented and redundant efforts between sponsors, sites and countries; the paucity of patients available for study in many paediatric indications and the need for multiple capable sites and expertise to make trials successful.”
This project aims to generate a sustainable infrastructure that optimises the delivery of clinical trials in children through:
- a single point of contact for all sponsors, sites and investigators
- efficient implementation of trials adopting consistent approaches, aligned quality standards and coordination of sites at national and international level
- collaboration with specialist and national networks
- high quality input to study design and preparation through rigorous strategic and operational feasibility assessment
- the promotion of innovative trial design and quantitative science methods
- an education and training platform to shape the future leaders of paediatric drug development
- the development of sustainable support for all these activities
One of the key goals of the project is to support the use of innovative trial designs and new quantitative methods to foster development of new innovative medicines and to support development in rare paediatric diseases and high medical need area
“Children must have access to innovative medical therapies that have been developed with the same degree of urgency and rigor as those for adults,” said Joanne Waldstreicher, MD, Chief Medical Officer, Johnson & Johnson. “With conect4children in Europe joining in this effort, complementing work under way with I-ACT for Children in the United States, we will be able to accelerate the availability of high quality scientific data that can improve the safe and effective use of therapies in children.”
“Clinical trials with medicinal products for paediatric use are one of the most sensitive areas in science – both from a medical and an ethical perspective”, said Dr. Michael Devoy, Chief Medical Officer of Bayer. “Improving the clinical trial infrastructure is an import step in enabling children to take part in medical progress”.
Dr. Mark Turner, Co-coordinator of the project, University of Liverpool, stated: “This network will have a significant impact on how we develop much-needed innovative and improved medicines for babies, children and young people. A number of collaborations built up over the past decade will contribute to this pan-European research network. The University of Liverpool is proud to be collaborating with institutions and research networks across Europe”
CVBF is involved in the project in the WP5 “Data coordinating centre and data quality standards” dedicated to enhance, through the provision and promotion of IT systems, tools, and standards, the quality, utility, reusability, and uniformity of data gathered from the studies performed by c4c, and to increase information on the network’s functioning at a central, national and site level. Moreover, CVBF will provide its contribution in WP6, by delivering short courses and e-training courses addressed to personnel involved in clinical trials management and organization, as well as by participating to the patients’ engagement activities also including the suggestions of YPAG (Young Patients Advisory Group). Finally, CVBF is also involved in the activities of WP8, developing format and contents of a campaign to raise awareness about paediatric research in the general population, and in personnel at children’s hospitals and medical schools.
With a budget of about 130 Mio€ (IMI2 support of 67 Mio€ and industry partners’ in-kind contribution of 73 Mio€), c4c is one of the biggest initiatives funded by the Innovative Medicines Initiative 2 Joint Undertaking (IMI2 JU) under grant agreement n º 777389. The Innovative Medicines Initiative 2 Joint Undertaking is Europe’s biggest Public Private Partnership and is funded jointly by the European Union´s Horizon 2020 research and innovation programme and the European pharmaceutical industry (represented by EFPIA, the European Federation of Pharmaceutical Industries and Associations).
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The parties involved
Under the name c4c, the new research consortium unites pharmaceutical companies, paediatric national networks as well as EU Multinational sub-specialty Networks, large patient advocacy groups, children’s hospitals and other public research organisations from across Europe. The full list of organisations involved in the project can be found at the c4c webpage www.conect4children.org
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This communication reflects the views of the c4c Consortium and neither IMI nor the European Union and EFPIA are liable for any use that may be made of the information contained herein
H2020-JTI-IMI2-2016-10. Proposal: 777389