Bukwang Pharm Starts Phase 2 Clinical Trial in the US for Parkinson's Disease Dyskinesia Treatment
[Asia Economy Reporter Chunhee Lee] Bukwang Pharmaceutical announced on the 29th that dosing has begun for the Phase 2 clinical trial of 'JM-010,' a treatment for Parkinson's disease dyskinesia, in the United States.
JM-010 is a new drug candidate developed by Conterapha, a Danish biotech venture and a subsidiary of Bukwang Pharmaceutical. It is expected to treat dyskinesia, which is known to occur with a 90% probability after more than 10 years of long-term use of 'Levodopa,' the drug primarily used to treat Parkinson's disease.
Bukwang Pharmaceutical is conducting clinical trials aiming for JM-010's approval in the United States, and Conterapha also initiated clinical trials last year in four European countries.
Bukwang Pharmaceutical stated, "With the dosing of the first patient this time as a milestone, we will register more patients to accelerate the clinical trial process and make every effort to soon provide LID as an essential treatment for Parkinson's disease patients."
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Bukwang Pharmaceutical aims to secure interim analysis results of JM-010 in 2022 and complete the clinical trial in 2023.
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