Key facts
- Principal investigator of the Tel Aviv natural history study of preclinical genetic CJD (NCT05746715) and first author of its protocol.
- Single site in Israel (Cognitive Neurology Unit, Tel Aviv Medical Center), recruiting; PI Noa Bregman; two groups: genetic CJD patients and first-degree healthy relatives (carriers and non-carriers of E200K); yearly in-depth visits for four years with clinical evaluation, blood and urine, gait, brain MRI, lumbar puncture and polysomnography; requires willingness to undergo genetic testing.
- Corresponding author of the BMC Neurology protocol (April 2023) for the cross-sectional and longitudinal study of patients and first-degree relatives.
- Co-author of the March 2025 JNNP paper on white matter abnormalities in healthy E200K carriers with raised CSF tau, funded by Ionis.
- The protocol aims to identify biomarkers of preclinical CJD and risk factors for phenoconversion in the largest known at-risk population.
- The registry lists individual participant data sharing as no.
Timeline
- 2023Registry listing updated.
- 2023Protocol published.
- 2025JNNP paper published.
Institutions
Projects and trials
Works with
This page covers public professional work only. To correct it or ask for it to be removed, write to hello@thegenerativebrain.org.
Last checked 16 October 2026
Sources for this page
- ClinicalTrials.gov NCT05746715: natural history study of preclinical genetic CJD (Tel Aviv Medical Center)
- Bregman et al., BMC Neurology 2023: natural history study of preclinical genetic CJD protocol (Tel Aviv)
- Omer et al., J Neurol Neurosurg Psychiatry 2025: white matter abnormalities in healthy E200K carriers