Study in Parkinson's Disease Patients With Dyskinesia With Combinations of JM-010 and Its Individual Components
Stopped early · Phase 2 · Has a placebo group
Conditions studied: Dyskinesias, Parkinson Disease
In brief
This is a two-part, double-blind, placebo-controlled, randomized, multicenter Phase 2 clinical trial of JM-010 in patients with Parkinson's Disease.
Key facts
- Study ID
- NCT04377945
- Run by
- Bukwang Pharmaceutical
- People needed
- 41
- Starts
- 2021-04-28
- Expected to finish
- 2024-02-14
- Last updated by the study team
- 2024-06-17
Who can join
Age: 18 and older, up to 85. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Is able to read, understand, and provide written, dated informed consent prior to Screening Visit.
- Is male or female, between 18 and 85 years of age at Screening Visit.
- Is diagnosed with idiopathic PD that meets UK Parkinson's Disease Society (UKPDS) Brain Bank Clinical Diagnostic Criteria
- Has experienced dyskinesia
- Has stable peak-effect dyskinesia
- Has more than one hour of "ON" time with troublesome dyskinesia
You may not qualify if…
- Has undergone surgery for the treatment of PD
- Has a current diagnosis of Substance Use
- Has psychiatric diagnosis of acute psychotic disorder or other psychiatric diagnoses
- Has current seizure disorders requiring treatment with anticonvulsants.
- Other criteria related to other medical conditions to be referred to the protocol.
Where it is running
- Bukwang Investigator site — Miami, Florida, United States
- Bukwang Investigator site — Detroit, Michigan, United States
Full record on ClinicalTrials.gov
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