Phase 2 Alzheimer's Disease Trial, Not Yet Recruiting NCT07611357 Sponsor: CellSight Technologies, Inc. Condition: Alzheimer's Disease
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Phase 2 Alzheimer's Disease Trial, Not Yet Recruiting

NCT07611357
Not Yet Recruiting Phase 2

voxsanity.com.au · Eligibility summary from public government registries · 18 August 2026 · not medical advice

Who may and may not 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 may be able to join

  • People aged 55 years or older.
  • People who have had a brain MRI scan available from a previous appointment (if the scan is more than 6 months old or not suitable, a new scan will be arranged).
  • People who are able to tolerate a PET scan and are willing and able to follow all the steps required by the study.
  • People who could potentially become pregnant and have not gone through menopause for at least 24 consecutive months, or have not had a hysterectomy, removal of both ovaries, or removal of both fallopian tubes, must be willing to use two effective forms of contraception (not including withdrawal or timing methods) up until 1 day after receiving the study imaging agent.
  • People who have been diagnosed with possible or probable Alzheimer's disease based on recognised medical guidelines for that diagnosis.
  • People who have a family member, carer, or close contact who spends significant time with them and can report on how they manage everyday activities.

Who may not be able to join

Each point below is a reason the trial team may not be able to accept someone. It is not a list of requirements to meet.

  • People who have a significant psychiatric condition other than depression.
  • People whose brain MRI shows structural problems (such as a large stroke or growth) that could interfere with reading the PET scan results.
  • People with a significant history of alcohol or substance misuse or dependence in the past 5 years.
  • People who have had a nuclear medicine imaging procedure or treatment using a radioactive substance (unrelated to this study) within 7 days before the PET scan.
  • People who are currently taking an experimental medication or have taken part in another experimental drug trial within the last 30 days.
  • People who have serious health conditions (cancer-related or otherwise) that, in the study doctor's opinion, could affect the goals of the study.
  • People who have conditions that affect how the immune system works, including known inflammatory or immune disorders, cancer affecting the whole body, or long-term viral infections, which could interfere with the imaging results.
  • People who are pregnant or currently breastfeeding (all participants who could potentially become pregnant will be asked to take a pregnancy test at the start of the study and on the day of the PET scan).
  • People who have previously received a stem cell transplant from another person, or a solid organ transplant.
  • People who have been diagnosed with myelodysplasia syndrome or a history of lymphoproliferative disease before joining the study (confirm with trial site).
  • People who have an active autoimmune disease affecting the whole body.
  • People who report a history of uncontrolled fear of enclosed spaces (claustrophobia).
  • People who have taken part in another research study that involved a PET scan done for research purposes within the last 12 months.
  • People whose body weight is more than 240 kg (529 pounds).
  • People who have recently used medications that contain guanosine or cysteine-like compounds (confirm with trial site).
  • People considered unsuitable for the study for any other reason, as determined by the lead study doctor.

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 13 August 2026

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Trial details

Status
Not Yet Recruiting
Phase
Phase 2
Sponsor
CellSight Technologies, Inc.
Registry
ClinicalTrials.gov
Start date
16 May 2026
Est. completion
16 September 2029

Primary endpoints

[¹⁸F]F-AraG uptake in the brain of patients with AD; [¹⁸F]F-AraG uptake kinetics in the brain of patients with AD; [¹⁸F]F-AraG vascular kinetics in the brain of patients with AD

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: 13 August 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