News

29 January 2025

Exciting News from the MACUSTAR .eu Consortium

The European public-private partnership consortium MACUSTAR .eu has received a thirdย ๐—Ÿ๐—ฒ๐˜๐˜๐—ฒ๐—ฟ ๐—ผ๐—ณ ๐—ฆ๐˜‚๐—ฝ๐—ฝ๐—ผ๐—ฟ๐˜ย from the European Medicines Agency (EMA) for its efforts in developing novel outcome measures for clinical trials evaluating treatments for the common eye condition age-related macular degeneration (AMD).

The scientific advice by the agency was based on four-year study results of more than ๐Ÿฒ๐Ÿฌ๐Ÿฌ ๐—˜๐˜‚๐—ฟ๐—ผ๐—ฝ๐—ฒ๐—ฎ๐—ป๐˜€ ๐˜„๐—ถ๐˜๐—ต ๐—ฒ๐—ฎ๐—ฟ๐—น๐˜† ๐˜€๐˜๐—ฎ๐—ด๐—ฒ๐˜€ ๐—ผ๐—ณ ๐—”๐— ๐—— who are at a high risk of developing visual impairment. EMA recognises the high quality and impact of the scientific outputs from theย ๐— ๐—”๐—–๐—จ๐—ฆ๐—ง๐—”๐—ฅย project that may have impact on more thanย 200 million patients with AMD globally.

The MACUSTAR consortium unites 20 EVICR.net clinical centers across 7 European countries, with the clinical study sponsored by UKB University of Bonn and AIBILI-Association for Innovation and Biomedical Research on Light and Image as the clinical trial unit coordinator.

This project has received funding from the Innovative Medicines Initiative 2 Joint Undertaking under grant agreement No 116076. This Joint Undertaking receives support from the European Unionโ€™s Horizon 2020 research and innovation programme and EFPIA. A further funding from Bayer, Novartis and Roche enabled the study to be extended by three years.

Read the EMA’s Full Letter of Support here: Letter of Support for intermediate Age-Related Macular Degeneration (AMD) biomarker and novel clinical endpoint development