Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Exebryl-1 is an orally bioavailable small-molecule amyloid- and tau-directed agent developed by ProteoTech as a potential disease-modifying therapy for Alzheimer’s disease, designed to prevent the formation, deposition, and accumulation of soluble and insoluble beta-amyloid species and to disaggregate existing amyloid plaques in the brain.[1][2][5][7][9][11] Preclinical data showed that Exebryl-1 reduces cerebral beta-amyloid load by approximately 30–50% in transgenic Alzheimer’s mouse models with associated memory improvement, and it also inhibits tau protein aggregation into paired helical filaments, targeting both amyloid plaques and neurofibrillary tangles.[1][5][7][9] The compound advanced into Phase 1 human clinical trials for mild-to-moderate Alzheimer’s disease and has also been identified in screening campaigns as a non-redox-reactive small-molecule inhibitor of the SARS-CoV-2 nsp15 endoribonuclease with modest antiviral activity, highlighting its potential as a chemical starting point for antiviral optimization.[1][3][10][12][13]
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on Exebryl-1.