Phase 2 Huntington'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 are willing and able to sign a consent form agreeing to take part in the trial.
- You are between 25 and 60 years old (inclusive) at the time of signing the consent form.
- You have been diagnosed with Spinocerebellar Ataxia Type 1 (SCA1), Spinocerebellar Ataxia Type 3 (SCA3), or Huntington's Disease (HD) at a mild-to-early stage, based on specific scoring systems used by doctors (confirm with trial site).
- Your diagnosis has been confirmed through genetic testing showing a specific type of gene change (an expanded DNA repeat) in the gene linked to your condition.
- There may be additional requirements to join — confirm all details with the trial site.
Who may not be able to join:
- You have any condition that would stop you from completing the trial's tests or assessments.
- You have genetic mutations in more than one disease-related gene beyond the one causing your diagnosed condition (confirm with trial site).
- You have been diagnosed with moderate or severe long-term migraines, or you have had a severe headache after a spinal tap (lumbar puncture) that needed hospital care or a special procedure to treat it.
- You have a condition affecting your brain, spine, or body that could interfere with a spinal tap procedure or make safety checks difficult.
- You have a history of blood clotting or bleeding problems, or your platelet count (cells that help blood clot) is lower than normal.
- You have an uncontrolled heart condition, a history of irregular heartbeat, an abnormal result on a heart tracing (ECG) test, or a family history of a serious inherited heart rhythm problem or sudden unexplained death.
- You have attempted suicide or have had serious thoughts of suicide with a plan that led to hospital admission or a change in your care within the last 12 months.
- You have medical, mental health, or other conditions that, in the doctor's opinion, might affect your ability to understand the trial, give consent, follow the trial rules, or complete the trial.
- You have previously been treated with a type of gene-targeting medicine called an antisense oligonucleotide or siRNA.
- You are pregnant, breastfeeding, or planning to become pregnant or breastfeed during the trial (applies to women).
- You are unable to have or tolerate MRI scans.
- There may be additional reasons that could prevent you from joining — confirm all details with the 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.
Contact this trial
Principal Investigator: Chief Medical Officer, VICO Therapeutics
Phone: +31 71 2036800
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 & dose relationships of treatment-related AEs, SAEs, AEs of special interest (AESI), severe events (NCI- CTCAE Grade 3 or higher).; Vital signs; Body weight; Electrocardiogram (ECG) RR interval; Electrocardiogram (ECG) - PR interval; Electrocardiogram (ECG) - QTc interval; Laboratory safety parameters in blood - white blood cell count; Laboratory safety parameters in blood - hemoglobin; Laboratory safety parameters in blood - platelets; Laboratory safety parameters in blood - prothrombin time (PT); Laboratory safety parameters in blood - activated partial thromboplastin clotting time...
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.