Ireland
--:--IST
Priya Life Science Compound trial record
Compound · clinical trials

Pridopidine clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 3 trials in our UK, USA, Germany, France, Spain, Italy, Netherlands, Belgium, Poland, Canada, Israel, Ireland, Sweden, Czechia and Portugal registers that name Pridopidine as an intervention. Synced 10 Nov 2026
3Current trials
2Recruiting now
2Lead sponsors
15Country registers
At a glance

Pridopidine is named as an intervention in 3 current clinical trials in our UK, USA, Germany, France, Spain, Italy, Netherlands, Belgium, Poland, Canada, Israel, Ireland, Sweden, Czechia and Portugal registers. 2 are recruiting patients now. The most common phase is Phase 3. The sponsor with the most trials is Prilenia (2). The most-studied condition is Amyotrophic Lateral Sclerosis. The EU clinical trials register (CTIS) separately lists 1 authorised or ongoing trial.

Where Pridopidine is approved

All regulators →
USUnited States (FDA)
No FDA approval of a single-substance product in Drugs@FDA
First original NDA/BLA approval
EUEuropean Union (EMA)
No centralised EU authorisation (it may be authorised nationally)
First centralised authorisation
CACanada (Health Canada)
No new-drug Notice of Compliance since 1994
First new-drug NOC

From the regulators' own registers: FDA Drugs@FDA, the EMA medicines list and Health Canada's Notice of Compliance database. Dates are the first listed approval of a product containing only this substance; combination products and nationally authorised EU medicines are not counted.

How Pridopidine works

All drug targets →
  • Dopamine D2 receptor modulator Modulator
    Target: DRD2 dopamine receptor D2
    ChEMBL only
Diseases it has been tested for in clinical trials, by furthest phase
  • Huntington diseasePhase 3
  • Amyotrophic lateral sclerosisPhase 3

Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL596802, CC BY-SA 3.0. Targets checked against the IUPHAR/BPS Guide to PHARMACOLOGY (2026.3.1), ligand 13833, CC BY-SA 4.0. Trial phases are not approvals: approved uses are shown from the regulators' own records where we hold them.

Patient leaflets for Pridopidine

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Reference identifiers for Pridopidine

ChEMBL
CHEMBL596802
DrugBank
DB11947
PubChem CID
9795739
CAS number
346688-38-8
FDA UNII
HD4TW8S2VK
Wikidata
Q7242858
Wikipedia
Pridopidine

Codes that identify this medicine in other databases, from Wikidata (CC0), matched by its ChEMBL ID. The ATC code is the WHO classification of what the medicine is used for.

Trials by status

  • Recruiting267%
  • Active, closed133%

Trials by phase

  • Phase 3267%
  • Phase 2/3133%
01

Clinical trials of Pridopidine

3 trials
StudyPhaseStatusLead sponsorRegisters
Pridopidine Phase 3 Study to Evaluate Efficacy and Safety in ALS
NCT07322003 · Amyotrophic Lateral Sclerosis
Phase 3 Recruiting Prilenia Ireland, UK, USA, Germany, France, Spain, Italy, Netherlands, Belgium, Sweden, Poland, Canada, Israel
Pridopidine Phase 3 Study in Huntington's Disease
NCT07609108 · Huntington Disease
Phase 3 Recruiting Prilenia UK, USA, Germany, France, Spain, Italy, Netherlands, Belgium, Poland, Czechia, Portugal, Canada
HEALEY ALS Platform Trial - Master Protocol
NCT04297683 · ClinicalTrials.gov ↗ · Amyotrophic Lateral Sclerosis
Phase 2/3 Active, closed Merit E. Cudkowicz, MD Israel

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Pridopidine in the EU trials register (CTIS)

1 trial

Authorised or ongoing trials in the EU Clinical Trials Information System that list a product containing Pridopidine. Many trials are registered in both CTIS and ClinicalTrials.gov, so these are shown separately rather than added to the count above. Trials with a site in Ireland are listed first.

StudyPhaseStatusSponsorCountries
A Phase 3, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Pridopidine in Participants with Huntington’s disease (HD).
2026-526093-16-00 · CTIS ↗ · Nervous System Diseases
Phase 3 Ongoing Ferrer Internacional S.A., Prilenia Therapeutics B.V Spain, Italy, Portugal + 6 more
03

Conditions studied with Pridopidine

2 conditions
04

Sponsors

lead sponsor per trial
Lead sponsorTrials
Prilenia2
Merit E. Cudkowicz, MD1
05

By country register

RegisterTrialsRecruiting
Clinical trials in UK22
Clinical trials in USA22
Clinical trials in Germany22
Clinical trials in France22
Clinical trials in Spain22
Clinical trials in Italy22
Clinical trials in Netherlands22
Clinical trials in Belgium22
Clinical trials in Poland22
Clinical trials in Canada22
Clinical trials in Israel21
Clinical trials in Ireland11
Clinical trials in Sweden11
Clinical trials in Czechia11
Clinical trials in Portugal11
EU register (CTIS)1—

A trial with sites in more than one country appears in each of those registers. CTIS does not publish a recruiting flag; its trials may also appear in the registers above.

06

Related compounds

07

Questions about Pridopidine trials

How many clinical trials are testing Pridopidine?

3 current trials in our UK, USA, Germany, France, Spain, Italy, Netherlands, Belgium, Poland, Canada, Israel, Ireland, Sweden, Czechia and Portugal registers name Pridopidine as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.

Are Pridopidine trials recruiting patients?

Yes. 2 of the 3 trials are recruiting: 2 with sites in UK, 2 with sites in USA, 2 with sites in Germany, 2 with sites in France, 2 with sites in Spain, 2 with sites in Italy, 2 with sites in Netherlands, 2 with sites in Belgium, 2 with sites in Poland, 2 with sites in Canada, 1 with sites in Israel, 1 with sites in Ireland, 1 with sites in Sweden, 1 with sites in Czechia and 1 with sites in Portugal. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Pridopidine clinical trials?

Prilenia (2) and Merit E. Cudkowicz, MD (1). The number in brackets is how many trials each organisation leads.

Are there Pridopidine clinical trials in Ireland?

Yes. 1 trial in our Ireland register (ClinicalTrials.gov). Some may be the same study registered in both. See the Irish clinical trials register for sites and contacts.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how Pridopidine works or whether it is effective, and it is not medical advice.

Approvals, shortages and trials, every Friday

One email a week with new EMA and FDA approvals, EU and US medicine shortages, how many trials are recruiting in Ireland, and the week's Irish pharma news.

Free. Unsubscribe from any email with one click. See our privacy policy.

How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how Pridopidine works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Pridopidine (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 10 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.