NCT03713957
Who may be able to join
Who might be able to join this trial:
- You have been diagnosed with Parkinson's Disease and have had symptoms for at least 1 year.
- You have been diagnosed with Parkinson's Disease along with mild memory or thinking problems, or Parkinson's-related dementia, based on recognized medical guidelines.
- Your score on a standard memory and thinking test (called the MoCA) falls between 13 and 25.
- Your Parkinson's symptoms are rated at a mild to moderately advanced stage (stages 1–4 on a standard scale used by doctors).
- Your score on a test that helps rule out stroke-related thinking problems is 4 or below (confirm with trial site).
Who may not be able to join:
- You have a history of problems with blood clotting or your blood clotting too easily.
- You are currently taking blood-thinning medication (note: common blood-thinning tablets like aspirin or clopidogrel are generally acceptable).
- You have previously had an allergic reaction to any human blood product or any medication given through a drip (IV infusion).
- You have received a human blood product, including a blood transfusion or IV immunoglobulin therapy, in the 6 months before joining the trial.
- You have a history of certain immune system deficiencies, or have previously had a stroke, severe allergic reaction, or blood clot complications related to IV immunoglobulin treatment (confirm with trial site).
- You have had a heart attack, unstable or severe chest pain, or heart failure in the 6 months before the trial begins.
- Your blood count (haemoglobin level) is too low — below a certain level for women or men respectively (confirm exact values with trial site).
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.
Trial details
Where this trial is recruiting
1 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
Incidence of Treatment-emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.