You’re using a public version of DrugPatentWatch with 5 free searches available | Register to unlock more free searches. CREATE FREE ACCOUNT

Last Updated: April 19, 2024

CLINICAL TRIALS PROFILE FOR PRIDOPIDINE


✉ Email this page to a colleague

« Back to Dashboard


Clinical Trials for Pridopidine

Trial ID Title Status Sponsor Phase Summary
NCT00665223 ↗ A Study of Treatment With Pridopidine (ACR16) in Patients With Huntington's Disease Completed Teva Branded Pharmaceutical Products R&D, Inc. Phase 3 The purpose of this study is to determine if ACR16 is effective and safe in the symptomatic treatment of Huntington's disease.
NCT00665223 ↗ A Study of Treatment With Pridopidine (ACR16) in Patients With Huntington's Disease Completed Teva Pharmaceutical Industries Phase 3 The purpose of this study is to determine if ACR16 is effective and safe in the symptomatic treatment of Huntington's disease.
NCT00724048 ↗ A Study of Pridopidine (ACR16) for the Treatment of Patients With Huntington's Disease Completed Teva Branded Pharmaceutical Products R&D, Inc. Phase 2/Phase 3 The purpose of this study is to determine if ACR16 is effective and safe in the symptomatic treatment of Huntington's Disease.
NCT00724048 ↗ A Study of Pridopidine (ACR16) for the Treatment of Patients With Huntington's Disease Completed Teva Pharmaceutical Industries Phase 2/Phase 3 The purpose of this study is to determine if ACR16 is effective and safe in the symptomatic treatment of Huntington's Disease.
NCT01306929 ↗ Open-label Extension Study of Pridopidine (ACR16) in the Symptomatic Treatment of Huntington Disease Completed Prilenia Phase 2 Huntington disease (HD) is a hereditary neurodegenerative disorder causing impairment in movement, behavioral dysfunction and dementia. The movement disorder is mainly characterized by chorea (involuntary movements) and a progressive loss of voluntary movement causing a substantial functional impairment over time. The study will assess the long-term safety of pridopidine and the treatment effects during long-term, open-label treatment.
NCT01306929 ↗ Open-label Extension Study of Pridopidine (ACR16) in the Symptomatic Treatment of Huntington Disease Completed Teva Branded Pharmaceutical Products, R&D Inc. Phase 2 Huntington disease (HD) is a hereditary neurodegenerative disorder causing impairment in movement, behavioral dysfunction and dementia. The movement disorder is mainly characterized by chorea (involuntary movements) and a progressive loss of voluntary movement causing a substantial functional impairment over time. The study will assess the long-term safety of pridopidine and the treatment effects during long-term, open-label treatment.
NCT02006472 ↗ A Phase 2, to Evaluating the Safety and Efficacy of Pridopidine Vs Placebo for Symptomatic Treatment in Patients With Huntington's Disease Completed European Huntington's Disease Network Phase 2 This is a multicenter, multinational, randomized, parallel-group, double-blind, placebo-controlled, dose range finding study to compare the efficacy and safety of different doses of pridopidine versus placebo in the treatment of motor impairment in Huntington's Disease (HD).
>Trial ID >Title >Status >Phase >Summary

Clinical Trial Conditions for Pridopidine

Condition Name

Condition Name for
Intervention Trials
Huntington Disease 3
Huntington's Disease 3
Amyotrophic Lateral Sclerosis 2
Health Volunteers, Huntington Disease 1
[disabled in preview] 0
This preview shows a limited data set
Subscribe for full access, or try a Trial

Condition MeSH

Condition MeSH for
Intervention Trials
Huntington Disease 7
Motor Neuron Disease 2
Amyotrophic Lateral Sclerosis 2
Parkinson Disease 1
[disabled in preview] 0
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Locations for Pridopidine

Trials by Country

Trials by Country for
Location Trials
United States 114
Canada 15
United Kingdom 11
Germany 9
France 7
This preview shows a limited data set
Subscribe for full access, or try a Trial

Trials by US State

Trials by US State for
Location Trials
Washington 7
New York 7
Pennsylvania 7
Ohio 6
Maryland 6
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Progress for Pridopidine

Clinical Trial Phase

Clinical Trial Phase for
Clinical Trial Phase Trials
Phase 3 2
Phase 2/Phase 3 3
Phase 2 4
[disabled in preview] 1
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Status

Clinical Trial Status for
Clinical Trial Phase Trials
Completed 5
Terminated 2
Active, not recruiting 1
[disabled in preview] 2
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Sponsors for Pridopidine

Sponsor Name

Sponsor Name for
Sponsor Trials
Prilenia 6
Teva Branded Pharmaceutical Products, R&D Inc. 4
Merit E. Cudkowicz, MD 2
[disabled in preview] 6
This preview shows a limited data set
Subscribe for full access, or try a Trial

Sponsor Type

Sponsor Type for
Sponsor Trials
Industry 15
Other 6
[disabled in preview] 0
This preview shows a limited data set
Subscribe for full access, or try a Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.