APTEEUS has received funding from the frontiers in Research Fund (NFRF) – 2022 Horizon Global Platform Program to participate in the multi-million Euro international SIMPATHIC consortium, established under the European Union’s ‘Horizon Europe’ funding stream.
APTEEUS, specialized in testing current medications on
tissues from the individual patient, is contributing to this capable
consortium by bringing its expertise in tailored research for genetic
About the SIMPATHIC Consortium
The SIMPATHIC Consortium, led by the Dutch Radboud University Medical Center and Amsterdam UMC, has developed a new approach to expedite the use of existing drugs for groups of patients with rare neurological disorders. The consortium has been awarded an 8.8 million euros grant from the Horizon Europe program to further develop this innovative method.
Traditionally, drugs are developed one disease at a time, which is costly and time-consuming. It often takes a long time before patients can use a new drug. The international SIMPATHIC Consortium, which comprises 22 international partners, has created a novel method for accelerating the use of existing drugs for other conditions, based on screening tissues from individual patients. The consortium’s approach has been recognized and funded by the European Commission with a 8.8 million euros grant.
The researchers will use a new technology to test the efficacy of existing drugs in patients with neurological disorders, requiring only a tube of blood or a small piece of skin from the patient. These materials contain stem cells that the researchers culture into nerve cells. They subsequently test how they respond to a variety of existing drugs.
If the researchers observe a positive effect of a drug, they will launch a clinical study in a group of patients with different disorders but similar clinical symptoms. As existing drugs have already been tested in humans, animal studies may not be necessary, which significantly accelerates the use of drugs in new applications and reduces research costs.
Project leader and bioinformatician Peter-Bram ‘t Hoen of Radboudumc explains: ‘The project will significantly improve the efficiency and speed of discovery, evaluation, and approval of new applications for existing drugs.‘
Project leader and pediatrician-biochemical geneticist Clara van Karnebeek of Amsterdam UMC adds: ‘In addition, it will have a huge impact on the care of patients with rare neurological disorders, for example, by accelerating drug availability for these debilitating conditions.‘