Results of a randomized, placebo‐controlled phase 1b study in MCI and mild AD patients with the orally available PRI‐002 with a unique mode of action.
PRI-002 was well tolerated. No biomarker changes have been found after 28 days of treatment. No ARIA were detected. Memory improved significantly in the verum group. The randomized, double-blind, placebo-controlled PRImus-AD phase 2 study has finished recruiting to assess safety and efficacy of PRI-002 in patients with MCI and mild dementia due to AD (EU CT# 2022-503148-41).
Authors
- Dagmar Jürgens
- Gunther Kauselmann
- Janine Kutzsche (ORCID: https://orcid.org/0000-0003-0271-7390)
- Nicoleta Carmen Cosma
- Dieter Willbold
- Oliver Peters
Institutions
- Forschungszentrum Jülich (DE)
- Humboldt-Universität zu Berlin (DE)
- Stadtwerke Jülich (Germany) (DE)
- Ministerium für Verkehr des Landes Nordrhein-Westfalen (DE)
- Heinrich Heine University Düsseldorf (DE)
- Franklin University (US)
- Freie Universität Berlin (DE)
- Charité - Universitätsmedizin Berlin (DE)
Publication Details
- Journal
- Alzheimer s & Dementia
- Published
- 2025-12-01
- DOI
- https://doi.org/10.1002/alz70859_101508
- Primary Topic
- Alzheimer's disease research and treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00