Phase 2 Alzheimer's Disease Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You have been diagnosed with mild memory or thinking problems, or mild dementia, caused by Alzheimer's disease.
- Any medications you currently take for Alzheimer's disease are expected to stay the same throughout the entire study.
- You are willing and able to take part in all parts of the study, including assessments, memory and thinking tests, and MRI scans.
Who may not be able to join:
- Your blood or urine tests at the screening appointment show significant abnormal results (confirm with trial site).
- You have a long-term liver condition.
- Your kidneys do not work well enough (confirm with trial site).
- You have high blood pressure that is not well controlled.
- You are currently taking any of the following medications: lithium, certain medications that can harm hearing, certain medications that can harm the kidneys, probenecid, or indomethacin (confirm with trial site if you are unsure whether your medications fall into these categories).
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Kyan Younes, MD, Stanford University
Phone: (650) 387-1559
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Incidence of Treatment-Related Adverse Events
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.