Phase 3 Huntington's Disease Trial, Terminated NCT00608881 Sponsor: Massachusetts General Hospital Condition: Huntington's Disease
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Trial results

AI generated results 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

According to the results reported on ClinicalTrials.gov, this trial looked at a high-dose form of a supplement called Coenzyme Q10 (2,400 mg per day) compared to a placebo (a dummy treatment with no active ingredient) in people with Huntington's disease. A total of 609 people took part — 303 in the Coenzyme Q10 group and 306 in the placebo group. The trial ran for 60 months (five years). The main thing being measured was a combined score that took into account both how long participants survived and how well they could manage everyday tasks and independent living — this was called a "joint rank" score. The reported data shows that on the main joint rank measure, the Coenzyme Q10 group received an average rank of 303.3 and the placebo group received an average rank of 306.7 — figures that were very close together. For the secondary measures, both groups showed declines over five years across all areas tested. The reported data shows that scores measuring ability to manage daily activities (Total Functional Capacity) fell by an average of 4.53 points in the Coenzyme Q10 group and 4.76 points in the placebo group (on a 0–13 scale). A daily task checklist (0–25 scale) dropped by 7.93 versus 8.02 points respectively. An independence scale (0–100) fell by 26.30 points in the Coenzyme Q10 group and 24.86 in the placebo group. A motor (movement) skills score (0–124, higher meaning more impairment) increased by 18.06 versus 19.18 points. Scores measuring behavioural symptoms increased by 1.39 versus 1.43 points across the two groups. These are the results as reported to ClinicalTrials.gov. They are not medical advice — always discuss what they mean for you with your doctor.

These are the results as reported to ClinicalTrials.gov, not medical advice. Verify independently with the trial site and discuss what they mean for you with your doctor.

Phase 3 Huntington's Disease Trial, Terminated

NCT00608881
Terminated Phase 3 🇦🇺 Australian site

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 have been diagnosed with Huntington's disease (HD) based on symptoms and family history, or confirmed through genetic testing showing a specific gene change linked to HD.
  • Your HD symptoms are still relatively mild, based on a standard assessment score above 9 (confirm with trial site).
  • You are able to walk around on your own and do not need professional nursing care.
  • You are 16 years of age or older.
  • If you are a woman, you are not able to become pregnant — either naturally (e.g., after menopause), through surgery, or by using reliable birth control throughout the study.
  • If you take certain mental health medications (such as anti-anxiety, sleep, or antidepressant medications), your dose has been stable for at least four weeks before joining and should stay the same during the study if possible.
  • You are able to understand and agree to the study procedures and give your consent to participate.
  • You are able to swallow oral (by mouth) medication.
  • You may need to have a trusted person (such as a family member or caregiver) who can help manage and supervise your daily medication at home.
  • You agree to name someone who can make decisions on your behalf if your ability to give consent changes during the study.

Who may not be able to join:

  • You have had a known bad reaction or sensitivity to Coenzyme Q10 (CoQ10) in the past.
  • You have taken part in another clinical trial or used an experimental drug within the past 30 days.
  • You have an unstable or serious physical health condition, as judged by the study doctor.
  • You have experienced serious mental health symptoms such as hallucinations, delusions, untreated severe depression, or thoughts of suicide within the past 90 days.
  • You have had a problem with alcohol or drug misuse within the past year.
  • You are currently pregnant or breastfeeding.
  • You have been taking CoQ10 supplements within the past 30 days.
  • Your recent blood test results show certain serious abnormalities in kidney function, liver function, blood cell counts, or blood clotting (confirm specific values with trial site).
  • You are allergic to a yellow food dye called FD&C Yellow #5, or to any other ingredient in the study medication.

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 28 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.

Contact this trial

Principal Investigator: Merit Cudkowicz, MD MSc, Massachusetts General Hospital

Australian sites

Westmead Hospital, Department of Neurology Level 1, Po Box 533, Wentworthville, New South Wales

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
Terminated
Phase
Phase 3
Registry
ClinicalTrials.gov
Start date
1 March 2008
Est. completion
1 November 2014

Where this trial is recruiting

🇦🇺 Australia 🇨🇦 Canada 🇺🇸 United States

1 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Joint Rank (Combination of Time to Death (for Subjects Who Died) and Change in Total Functional Capacity Score (TFC) From Baseline to Month 60 (for Subjects Who Survived))

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: 28 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