RecruitingPhase 2NCT07312110

D-SPARK: A Clinical Trial of D-Serine for Modifying Parkinson's Disease Progression

D-SPARK: A Randomized Double Blind Clinical Trial of D-Serine for Modifying Parkinson's Disease Progression


Sponsor

Haukeland University Hospital

Enrollment

100 participants

Start Date

Jan 1, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This clinical study, designed as a randomized, double-blind, placebo-controlled trial, aims to investigate if modulation of the N-methyl-D-aspartate receptor (NMDAR) via its co-agonist D-serine has therapeutic benefits in Parkinson's disease (PD). All patients will receive both placebo and D-serine over different time periods during the study. Preclinical studies have shown that blocking glycine transporters, which elevates endogenous glycine levels, can restore NMDAR function and improve motor deficits in PD models. A clinical trial demonstrated that oral D-serine (30 mg/kg/day for 6 weeks) significantly reduced extrapyramidal and abnormal involuntary movements in PD patients compared to placebo, with improvements observed in both motor and non-motor symptoms. D-serine supplementation has shown an acceptable safety profile with doses up to 120 mg/kg showing no significant adverse effects in clinical studies. The D-SPARK trial primarily aims to determine the efficacy of D-serine supplementation on clinical severity of PD as measured by the Movement Disorder Society Unified Parkinson's Disease Rating Scale (MDS-UPDRS). Secondary aims are to determine the efficacy of D-serine supplementation on improving dopaminergic nigrostriatal innervation as measured by single-photon emission tomography (SPECT) based imaging of the dopamine transporter (DaT-scan) and cognition as measured by the California Verbal Learning Test version 2 (CLVT-II). The study will include 100 persons with Parkinson's disease (PwPD) diagnosed no longer than 5 years before baseline. Participants will be randomly assigned to receive D-Serine 4000 mg daily or placebo for defined periods of time during a 58 week treatment period, followed by a 12 week washout period. Participants will undergo: * Clinical evaluations, including clinical rating scales and questionnaires. * Cognitive assessments. * Bio sampling of whole blood and blood plasma. * Single-photon emission tomography (SPECT) imaging of dopamine transporter levels (DaT-scan) The outcomes of this study could potentially demonstrate that D-serine reduces symptom severity in Parkinson's disease and/or has an impact on the clinical trajectory of Parkinson's disease, benefiting persons living with Parkinson's disease, their families and society as a whole.


Eligibility

Min Age: 40 YearsMax Age: 80 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial tests whether D-serine — an amino acid naturally found in the brain — can slow the progression of Parkinson's disease. It is being studied in people with a recent Parkinson's diagnosis to see if it can protect nerve cells from further damage. **You may be eligible if...** - You have been diagnosed with Parkinson's disease within the past 5 years according to standard criteria - A brain scan (DaTscan) confirmed the typical pattern of Parkinson's in your brain - Your Parkinson's is still in an early to moderate stage (Hoehn & Yahr score less than 3) - You are between 40 and 80 years old - Your current Parkinson's treatments have been stable for at least 2 weeks **You may NOT be eligible if...** - You have dementia or another neurodegenerative disease - Your Parkinson's is advanced - You have a serious kidney or liver condition Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIETARY_SUPPLEMENTD-serine

D-serine 2 x 500 mg and 2 x Placebo oral capsules administered twice daily the first week of intervention, then uptitrated to D-serine 4 x 500 mg twice daily for the remainder of the intervention.

DIETARY_SUPPLEMENTPlacebo

Placebo 2 x oral capsules administered twice daily.


Locations(11)

Sørlandet Hospital Arendal

Arendal, Agder, Norway

Akershus University Hospital

Lørenskog, Akershus, Norway

Vestre Viken Hospital

Drammen, Buskerud, Norway

Molde Hospital

Molde, Møre og Romsdal, Norway

Bodø Hospital (Nordland Hospital)

Bodø, Nordland, Norway

Oslo University Hospital

Oslo, Oslo, Norway

Haugesund Hospital

Haugesund, Rogaland, Norway

University Hospital of North Norway

Tromsø, Troms, Norway

Haukeland University Hospital

Bergen, Vestland, Norway

Førde Hospital

Førde, Vestland, Norway

Østfold Hospital

Sarpsborg, Østfold fylke, Norway

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NCT07312110


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