Phase 2 Alzheimer's Disease Trial, Recruiting NCT07693140 Sponsor: Evan Thomas Condition: Alzheimer's Disease
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Phase 2 Alzheimer's Disease Trial, Recruiting

NCT07693140
Recruiting Phase 2

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:

  • People who are aged 50 or older at the time of joining the trial
  • People who have received a confirmed diagnosis from a neurologist or geriatric psychiatrist of Alzheimer's disease, frontotemporal dementia with signs of brain inflammation, dementia with Lewy bodies with certain inflammation markers, or another neurodegenerative dementia where inflammation in the brain has been confirmed
  • People whose score on a standard memory and thinking test (called the MoCA) falls between 10 and 25, indicating mild to moderate cognitive impairment
  • People who are reasonably physically functional, as measured by standard performance scales used by doctors (confirm with trial site)
  • People who are medically stable and assessed by a radiation specialist as able to safely receive radiation therapy
  • People who have a reliable carer or close contact who is able to attend at least 80% of the scheduled appointments with them
  • People (or their legal representative) who are able to give written consent to participate; a carer's co-consent is also required
  • People whose doctor estimates they have a life expectancy of at least 18 months
  • People who are willing and able to attend monthly clinic visits over a 12-month period

Who may not be able to join:

  • People who have previously received any radiation therapy to the whole brain or part of the brain at any time
  • People who currently have an active cancer elsewhere in the body that requires ongoing cancer treatment
  • People who have an implanted medical device that is not compatible with radiation therapy, such as a pacemaker, cochlear implant, or deep brain stimulator
  • People whose brain MRI shows certain concerning findings, including more than 4 small bleeds, more than 1 area of a specific type of surface bleeding, severely damaged white matter, or any larger bleed or blood stain greater than 10mm (confirm with trial site)
  • People with a known active condition involving inflammation related to amyloid protein buildup in the brain's blood vessels, whether confirmed by biopsy, fluid analysis, or brain imaging
  • People currently in the acute (active flare) phase of an autoimmune brain condition — those in a stable chronic phase may still be considered
  • People with an uncontrolled infection or active blood poisoning (sepsis) at the time of joining
  • People with severe, active psychiatric conditions such as psychosis or active suicidal thoughts that could affect their safety or ability to follow the study procedures
  • People who are already enrolled in another interventional clinical trial targeting memory decline or brain inflammation
  • People who are pregnant or breastfeeding; women who could become pregnant must use adequate contraception
  • People who are unable to lie flat and still for approximately 10 to 15 minutes during each radiation session
  • People whose MoCA score is below 10, indicating severe dementia

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 22 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Evan Thomas, MD, PhD, Renaissance Institute of Precision Oncology and Radiosurgery

Phone: 321-972-1102

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

Status
Recruiting
Phase
Phase 2
Sponsor
Evan Thomas
Registry
ClinicalTrials.gov
Start date
15 July 2026
Est. completion
21 May 2029

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Safety, As Measured By Incidence of Grade 3 or Higher Treatment-Related Adverse Events

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 22 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov