Press

1.3-million-euro funding for the Eurostars project MastCURe: The Fraunhofer Institute for Translational Medicine and Pharmacology ITMP Immunology and Allergology IA in Berlin will conduct research over the next 3 years together with Allegria Therapeutics and Cube Biotech on a novel therapeutic approach to treating chronic urticaria.

A milestone in the treatment of Leigh syndrome, a rare, early-onset disease in children, has been reached: At the Hamburg site of the Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, in collaboration with Heinrich Heine University Düsseldorf (HHU) and University Hospital Düsseldorf (UKD), as well as Charité – Universitätsmedizin Berlin, a promis-ing agent for the treatment of Leigh syndrome was identified. The researchers were able to demonstrate a positive effect of the active substance sildenafil on the disease course.

From molecules to realistic therapeutic approaches: Fraunhofer ITMP receives fund-ing for three translational projects developing new treatment methods for rare, hard-to-treat diseases in infancy or early childhood.

Dr. Shara Safarian took up a visiting professorship at the Institute of Translational Medicine at the First Hospital of Jilin University in China in October. The appointment is part of a scientific exchange agreement and is intended to further intensify international cooperation. At the same time, it strengthens the strategic positioning of the Fraunhofer ITMP on the Chinese research market.

The official dedication of the new building on the Niederrad campus marks a fresh milestone in the research landscape of the state of Hesse, set by the Fraunhofer Institute for Translational Medicine and Pharmacology ITMP. Some 200 prominent representatives from government, the science and research sector, industry and the trades involved in the building project gathered for the opening celebration at the invitation of Gerd Geisslinger, executive director of Fraunhofer ITMP. The new research building will serve as a locus of expertise in translational medicine while strengthening Hesse as a hub of pharmaceutical and biotech activity.

Researchers at Fraunhofer ITMP have identified a promising approach for children affected by KCNQ2-related epilepsy. A drug originally developed as an antipsychotic has shown the ability to activate KCNQ2 potassium channels and significantly reduce seizure-like activity. The findings, based on patient-derived brain cells and animal models, suggest the potential of repurposing this compound into much‑needed therapy, opening up new hope for affected families.

The SLAS Europe Conference and Exhibition, one of the most important events in the field of laboratory automation and screening, took place in Hamburg for the first time from May 20 to 22, 2025 – with great success. The Fraunhofer Institute for Translational Medicine and Pharmacology ITMP was represented with a varied program and set technical highlights.

The SYNTHIA project, a groundbreaking public-private partnership funded by the Innovative Health Initiative (IHI), is set to revolutionize the field of personalized medicine by harnessing the power of synthetic data. As the first IHI project to tackle the critical need for privacy-preserving data solutions in healthcare, SYNTHIA aims to propel research and innovation to new heights, ensuring that patients receive the best possible care while safeguarding their personal information.

It is known that malfunctions of the proteins FLVCR1 and FLVCR2 lead to rare hereditary diseases in humans that cause motor, sensory and neurological disorders. However, the biochemical mechanisms behind this and the physiological functions of the FLVCR proteins have been unclear to date. An interdisciplinary team of researchers from Frankfurt am Main, Singapore and the USA has now deciphered the FLVCR proteins’ 3D structures and their cellular functions. The researchers have shown that the proteins transport the cellular building blocks choline and ethanolamine. Their findings contribute significantly to understanding the pathogenesis of rare diseases and developing new therapies.