Autosomal recessive early-onset Parkinson disease 6
MONDO:0011613Any Parkinson disease in which the cause of the disease is a mutation in the PINK1 gene.
Also known as: PINK1 Parkinson disease, Parkinson disease caused by mutation in PINK1, autosomal recessive early-onset Parkinson disease 6, PARK6, Parkinson disease 6, autosomal recessive early-onset, Parkinson disease 6, early onset, Parkinson disease 6, early-onset, Parkinson disease 6, late-onset, susceptibility to
16 clinical trials for this condition and its sub-types, 4 tagged with Autosomal recessive early-onset Parkinson disease 6 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →-
Can a new pill slow Parkinson's symptoms?
Disease control Not yet recruitingThis clinical trial is testing an experimental medication called TJ0113 in people with early-onset Parkinson's disease. The study aims to see if TJ0113 can improve movement symptoms compared to a placebo. About 300 participants will take either TJ0113 or a placebo for 26 weeks, f…
Phase 3 • Sponsor: Hangzhou PhecdaMed Co., Ltd. • Aim: Disease control
Last updated Aug 14, 2026 00:00 UTC
-
Scientists launch 5-year watch on rare genetic Parkinson's to unlock disease secrets
Knowledge-focused Not yet recruitingThis study follows 70 people with PRKN- or PINK1-linked Parkinson's disease, as well as those with typical Parkinson's and healthy volunteers, over 5 years. Researchers will track movement, thinking, and mood symptoms, and collect blood, urine, and optional spinal fluid or muscle…
Sponsor: National Institute of Neurological Disorders and Stroke (NINDS) • Aim: Knowledge-focused
Last updated Sep 20, 2026 00:00 UTC