Phase 3 Parkinson's Disease Trial, Recruiting NCT07316296 Sponsor: Radboud University Medical Center Condition: Parkinson's Disease
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Phase 3 Parkinson's Disease Trial, Recruiting

NCT07316296
Recruiting Phase 3

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 aged 18 years or older
  • People who have been diagnosed with idiopathic Parkinson's disease (Parkinson's that has no known cause) using internationally recognised diagnostic guidelines
  • People whose Parkinson's medication has been stable and at the best-possible dose for at least four weeks before the trial starts, and who are expected to remain stable throughout the trial
  • People who experience freezing of gait (sudden episodes where the feet feel "stuck" to the ground) on a daily basis
  • People who are able to walk 10 metres without assistance while their Parkinson's medication is working well
  • People who are able to sign a written consent form in line with research regulations
  • People who are willing and able to attend and complete all assessments required by the trial

Who may not be able to join:

  • People who are currently in another clinical trial, or who have participated in one within the past three months
  • People who cannot have an MRI scan for any reason — for example, due to claustrophobia, or because they have metal devices inside their body such as a deep brain stimulator, infusion pump, or pacemaker
  • People who have another medical condition that significantly affects their ability to walk, such as bone or joint problems
  • People with severe difficulties with thinking or memory that would make it hard to follow the trial's requirements
  • People with active psychosis (such as hallucinations or delusions) that would make it hard to follow the trial's requirements
  • People with serious heart conditions, including very high blood pressure, heart failure, blocked arteries, angina, significant heart disease present from birth, heart muscle disease, previous heart attack, potentially life-threatening irregular heartbeats, long QT syndrome, or certain inherited heart rhythm disorders — where the trial doctor considers these to be a significant safety concern
  • People with serious brain blood vessel conditions, such as a brain aneurysm or a recent or significant stroke
  • People with liver or kidney problems that the lead trial doctor considers would make participation unsafe
  • People with a specific type of eye pressure condition called narrow-angle glaucoma
  • People who have, or have had, a rare adrenal gland tumour called a phaeochromocytoma
  • People who are currently taking medications that affect the noradrenaline system (noradrenergic agents) (confirm with trial site)
  • People who are currently taking certain medications that affect how the body processes drugs, including some antidepressants (SSRIs), quinidine, or terbinafine (an antifungal medicine)
  • People taking high doses of salbutamol or similar medicines (called beta-2 agonists), where the lead trial doctor considers this would affect safe participation
  • People who are pregnant or breastfeeding
  • People who have a known allergy or sensitivity to atomoxetine (the medicine being studied in this trial)

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 26 July 2026
Phase 3: approximately ~65% 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.

GP referral letter

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Trial details

Status
Recruiting
Phase
Phase 3
Registry
ClinicalTrials.gov
Start date
1 January 2026
Est. completion
1 July 2027

Where this trial is recruiting

🇳🇱 Netherlands

Primary endpoints

The percentage of time frozen in the dopaminergic OFF-state

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: 26 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