400 Participants NeededMy employer runs this trial

Pridopidine for Huntington's Disease

(PRECISE-HD Trial)

Recruiting at 65 trial locations
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Overseen ByPrilenia Medical Information
Pivotal Trial (Near Approval)This treatment is in the last trial phase before FDA approval
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests whether the drug pridopidine can slow the progression of Huntington's Disease (HD) over a year. Researchers aim to determine if pridopidine improves everyday tasks, cognitive function, muscle movement, and overall quality of life compared to a placebo (a pill with no active drug). Suitable candidates for this trial are adults diagnosed with HD who have noticeable movement issues and have not taken certain medications in the past six months. Participants will take a capsule twice daily for a year and visit the clinic six times for check-ups. After the first year, all participants will receive pridopidine for an additional two years. As a Phase 3 trial, this study represents the final step before FDA approval, offering participants a chance to contribute to potentially groundbreaking treatment advancements.

Do I have to stop taking my current medications for the trial?

The trial requires that you have not used certain medications, like antipsychotics, for at least 6 months before starting. It's not encouraged to stop these medications just to join the trial. If you're on medications that prolong the QT interval, you need to stop them 4 weeks before the trial.

Is there any evidence suggesting that pridopidine is likely to be safe for humans?

Research has shown that pridopidine has been tested in over 1,700 people, with some using it for up to seven years. The findings indicate that it is generally safe and well-tolerated. In a study of 1,067 patients with Huntington's Disease (HD), pridopidine's side effects were similar to those of a placebo, a harmless substance used for comparison. So far, pridopidine has demonstrated a good safety record, with no major safety concerns reported. This suggests that most people can use the treatment without serious problems.12345

Why do researchers think this study treatment might be promising for Huntington's Disease?

Pridopidine is unique because it offers a novel approach to treating Huntington's disease by targeting the sigma-1 receptor, which plays a key role in neuroprotection and cellular function. Unlike current treatments, such as tetrabenazine and deutetrabenazine, which primarily focus on managing symptoms like chorea through dopamine depletion, pridopidine aims to preserve and enhance neuronal health. Researchers are excited about pridopidine because it holds the potential not just to alleviate symptoms, but also to modify the underlying disease progression, offering hope for long-term improvement in patients' quality of life.

What evidence suggests that pridopidine might be an effective treatment for Huntington's Disease?

Research has shown that pridopidine might help treat Huntington's Disease. In this trial, participants will receive either pridopidine or a placebo. Studies have found that pridopidine can slow the disease's progression and improve patients' movement abilities. For example, patients taking pridopidine scored better on a test measuring movement problems. Additionally, pridopidine helped patients maintain daily activities. Most people can take this treatment without serious side effects, indicating it is generally well-tolerated. These findings suggest that pridopidine could help manage symptoms of Huntington's Disease.12467

Are You a Good Fit for This Trial?

This trial is for adults (21 or older) diagnosed with Huntington's Disease, confirmed by genetic testing. Participants must have clear movement symptoms, be able to do some daily activities on their own, and not be taking certain psychiatric medications for at least 6 months before joining.

Inclusion Criteria

My Independence Scale score is 90% or less.
Cytosine-Adenine-Guanine (CAG)-Age Product (CAP)100 score ≥95 at Screening
Diagnostic confidence level (DCL) of 4 (unequivocal motor signs, ≥99% confidence) on standardized motor exam Total Motor Score (TMS)
See 5 more

Exclusion Criteria

I do not have any active or recently treated cancer, unless it was localized and is now resolved.
I have used mutant huntingtin-lowering therapy in the past year.
I have not taken medicines that affect my heart's QT interval in the past 4 weeks.
See 9 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive either pridopidine or placebo for 1 year, starting with a 2-week titration period followed by twice-daily dosing

52 weeks
6 in-clinic visits, 5 telephone visits

Open-label Extension

All participants receive pridopidine for an additional 2 years, starting with a 2-week retitration period followed by twice-daily dosing

104 weeks
6 in-clinic visits, 6 telephone visits

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Pridopidine

Trial Overview

The study tests whether pridopidine can slow the progression of Huntington's Disease compared to a placebo. For one year, participants take either pridopidine or placebo capsules twice daily. Afterward, all receive pridopidine for two more years.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Placebo Group

Group I: PridopidineExperimental Treatment1 Intervention
Group II: PlaceboPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Prilenia

Lead Sponsor

Trials
8
Recruited
1,500+

Ferrer Internacional S.A.

Industry Sponsor

Trials
27
Recruited
11,700+

Citations

Pridopidine for the Improvement of Motor Function in Patients ...

Patients in the pridopidine group had a significantly lower Unified Huntington's Disease Rating Scale (UHDRS)-modified Motor Score (mMS) (MD −0.79, 95% CI = − ...

Nature Medicine Publishes Phase 3 Data on Pridopidine in ...

The publication describes data showing that treatment with pridopidine slowed clinical progression in Huntington's disease (HD) patients not ...

NCT07609108 | Pridopidine Phase 3 Study in Huntington's ...

The goal of this clinical trial is to learn if pridopidine can slow the clinical decline of Huntington's Disease (HD) in adult participants.

Pridopidine in early-stage manifest Huntington's disease

Results consistently favored pridopidine over placebo at time points between weeks 26 and 78, supporting a potential treatment effect on motor ...

Analyses of the Phase 3 Trial of Pridopidine's Outcome on ...

In analyses excluding participants on ADMs, pridopidine significantly improves or stabilizes all outcome measures for at least 1 year and was ...

The Safety Profile of Pridopidine, a Novel Sigma-1 Receptor ...

An integrated safety analysis of 1067 patients with HD showed that pridopidine is generally safe and well tolerated with an adverse event ...

Press Release Details - Newsroom | Prilenia Therapeutics B.V.

In clinical studies to date, pridopidine has shown a generally favorable safety and tolerability profile, with data from more than 1,600 people ...