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Evaluation of [¹⁸F]MODAG-009 PET Imaging in Synucleinopathies (MODAG-009-P1-0)

6 juni 2026 uppdaterad av: MODAG GmbH
This is a single-center, open-label clinical study designed to evaluate the imaging characteristics and safety of [¹⁸F]MODAG-009 in participants with Parkinson's disease (PD), Multiple system atrophy (MSA), and Healthy controls (HC). Approximately 13 participants will be enrolled in this study. Each participant will receive a single intravenous injection of [¹⁸F]MODAG-009, followed by PET imaging using the investigational United Imaging NeuroEXPLORER (NX) camera.

Studieöversikt

Detaljerad beskrivning

This is a single-center, open-label clinical study designed to evaluate the imaging characteristics and safety of [¹⁸F]MODAG-009 in participants with PD, MSA, and HC.

All eligible participants receive a single IV injection of [¹⁸F]MODAG-009 followed by dynamic PET imaging using the United Imaging NeuroEXPLORER (NX) brain PET scanner for up to 3 hours post-injection, according to an Image Acquisition Plan (IAP). Structural MRI (obtained under PPMI-002 or as part of routine care/screening) is used for anatomical localization and region-of-interest definition. Safety assessments include physical examination, vital signs, ECG, safety laboratory tests, and AE monitoring on the imaging day and at a follow-up contact 2-3 business days after tracer injection. Blood sampling is performed for radiometabolite analysis and to support quantitative interpretation of PET data, as specified in the IAP.

Approximately 13 participants will be enrolled in this study. All PD and HC participants will be enrolled from the ongoing PPMI 002 Clinical study at the INDD site. Leveraging the existing PPMI cohort allows use of previously collected clinical and biomarker data, thereby minimizing participant burden and ensuring alignment with established study assessments. The MSA cohort will be enrolled from the general population.

Studietyp

Interventionell

Inskrivning (Beräknad)

13

Fas

  • Tidig fas 1

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

  • Namn: Johannes Levin, MD
  • Telefonnummer: 475-318-8250 (24 hours)
  • E-post: Levin@modag.net

Studieorter

    • Connecticut
      • New Haven, Connecticut, Förenta staterna, 06510
        • Rekrytering
        • Institute for Neurodegenerative Disorders and XingImaging, LLC
        • Huvudutredare:
          • Neha Prakash, MBBS
        • Kontakt:

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Ja

Beskrivning

Inclusion Criteria:

  • Healthy Controls inclusion criteria:

    1. Enrolled in the PPMI 002 Clinical study as a healthy control participant
    2. Any gender aged 50 to 75 years of age
    3. Negative CSF α-synuclein seed amplification assay (SAA)
    4. Previously acquired (since inclusion in PPMI) brain MRI without evidence of significant neurological pathology.
    5. Movement Disorders Society- Unified Parkinson's Disease Rating Scale Part III (MDS-UPDRS III) score of <6 at the last PPMI annual visit which is within the past 18 months.
    6. Cognitively intact with Montreal Cognitive Assessment (MoCA) greater than or equal to 26 at the last PPMI annual visit which was within the past 18 months.
  • Parkinson's Disease and Prodromal PD inclusion criteria:

    1. Enrolled in the PPMI 002 Clinical study as a Parkinson's Disease (PD) or Prodromal participant
    2. Any gender aged 50 to 80 years of age
    3. Positive CSF SAA
    4. A current or previously acquired brain MRI (since the onset of motor symptoms for PD or since enrolled in PPMI for the prodromal PD) without evidence of significant neurological pathology other than changes expected for PD.
    5. Montreal Cognitive Assessment (MoCA) greater than or equal to 24 at the last PPMI annual visit which was within the past 18 months.
  • Multiple System Atrophy (MSA) inclusion criteria:

    1. Any gender aged 50 to 75 years of age
    2. Clinically established MSA or Clinically Probable MSA according to the Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy (Wenning et al., 2022)
    3. Positive CSF SAA
    4. A current or previously acquired brain MRI (since the onset of motor symptoms attributed to MSA) without evidence of significant neurological pathology other than the pathology expected for MSA.
    5. Evidence of nigrostriatal degeneration on DaTscan obtained at screening or on previously acquired imaging since the onset of the motor symptoms attributed to MSA.

Exclusion Criteria:

  • All Cohorts:

    1. Clinical evidence of other neurodegenerative diseases, such as Alzheimer's disease
    2. Any other medical or psychiatric condition or lab abnormality, which in the opinion of the investigator might preclude participation.
    3. Received any of the following drugs: dopamine receptor blockers (neuroleptics), metoclopramide, lithium and reserpine, within 6 months of Baseline Visit.
    4. Any other reason that in the opinion of the investigator, including abnormal labs, that could interfere with the safety with radiotracer injection, would render the participant unsuitable for the study enrollment.
    5. Participation in an investigational drug trial targeting α-synuclein within the past 6 months prior to enrollment.
    6. Currently being treated with and unable to safely hold antiplatelets (other than low dose aspirin up to 100mg/day) or anticoagulants prior to the procedure that might preclude safe attempt of Lumbar puncture, if applicable.
    7. Condition that precludes the safe performance of routine lumbar puncture, if applicable, such as prohibitive lumbar spinal disease, bleeding diathesis, or clinically significant and uncorrected coagulopathy or thrombocytopenia.
    8. Conditions or medications that preclude safe performance of imaging procedures (MRI or DaTscan), including but not limited to severe claustrophobia, MRI-incompatible metal implants, or known hypersensitivity to imaging agents.
    9. Known hypersensitivity to DaTscan or iodine-containing compounds used as premedication for DaTscan. Participants with iodine sensitivity may still complete the imaging without iodine premedication at the investigator's discretion.
    10. Use of medications known to interfere with DaTscan imaging (e.g., bupropion, amphetamines, methylphenidate, modafinil, alpha-methyldopa), unless the participant is willing and medically able to hold the medication for at least 5 half-lives or specified duration per investigators judgement prior to imaging.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Diagnostisk
  • Tilldelning: N/A
  • Interventionsmodell: Enskild gruppuppgift
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Parkinson's disease (PD); Multiple system atrophy (MSA); Healthy controls (HC)
Participants enrolled in the study will receive a single IV injection of up to up to 8 mCi of [¹⁸F]MODAG-009.
Participants enrolled in the study will receive a single IV injection of [¹⁸F]MODAG-009 followed by dynamic PET imaging using the United Imaging NeuroEXPLORER (NX) brain PET scanner.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Standard Uptake Value Ratios (SUVR)
Tidsram: Up to 3 hours after tracer injection.
To evaluate Standard Uptake Value Ratios (SUVR) in brain regions from [18F]MODAG-009 in participants with PD.
Up to 3 hours after tracer injection.
Standard Uptake Value Ratios (SUVR)
Tidsram: Up to 3 hours after tracer injection.
To evaluate Standard Uptake Value Ratios (SUVR) in brain regions from [18F]MODAG-009 in participants with MSA.
Up to 3 hours after tracer injection.
Standard Uptake Value Ratios (SUVR)
Tidsram: Up to 3 hours after tracer injection.
To evaluate Standard Uptake Value Ratios (SUVR) in brain regions from [18F]MODAG-009 in HC participants.
Up to 3 hours after tracer injection.

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Safety, tolerability, and feasibility
Tidsram: From baseline to follow-up 2-3 business days after tracer injection.
To assess the number and severity of adverse events following administration of [18F]MODAG-009 tracer in human participants.
From baseline to follow-up 2-3 business days after tracer injection.
Safety, tolerability, and feasibility
Tidsram: From baseline to follow-up 2-3 business days after tracer injection.
To assess blood pressure [mmHg] following administration of [18F]MODAG-009 tracer in human participants.
From baseline to follow-up 2-3 business days after tracer injection.
Safety, tolerability, and feasibility
Tidsram: From baseline to follow-up 2-3 business days after tracer injection.
To assess heart rate [Hz] following administration of [18F]MODAG-009 tracer in human participants.
From baseline to follow-up 2-3 business days after tracer injection.
Safety, tolerability, and feasibility
Tidsram: From baseline to follow-up 2-3 business days after tracer injection.
To assess body temperature [°C] following administration of [18F]MODAG-009 tracer in human participants.
From baseline to follow-up 2-3 business days after tracer injection.
Safety, tolerability, and feasibility
Tidsram: From baseline to follow-up 2-3 business days after tracer injection.
To assess the treatment-emergent changes in physical examination following administration of [18F]MODAG-009 tracer in human participants.
From baseline to follow-up 2-3 business days after tracer injection.
Safety, tolerability, and feasibility
Tidsram: From baseline to follow-up 2-3 business days after tracer injection.
To assess changes the clinical laboratory tests including hematology and clinical chemistry including renal function tests, hepatic enzymes, electrolytes and creatine kinase following administration of [18F]MODAG-009 tracer in human participants.
From baseline to follow-up 2-3 business days after tracer injection.
Safety, tolerability, and feasibility
Tidsram: From baseline to follow-up 2-3 business days after tracer injection.
To assess drop-out/early discontinuation following administration of [18F]MODAG-009 tracer in human participants.
From baseline to follow-up 2-3 business days after tracer injection.
Safety, tolerability, and feasibility
Tidsram: From baseline to follow-up 2-3 business days after tracer injection.
To assess 12-lead ECG parameters including QT interval corrected for heart rate using Fridericia's formula (QTcF) following administration of [18F]MODAG-009 tracer in human participants.
From baseline to follow-up 2-3 business days after tracer injection.
Regional brain uptake
Tidsram: Up to 3 hours after tracer injection.
To determine regional brain uptake of [¹⁸F]MODAG-009 and binding patterns associated with α-synuclein pathology.
Up to 3 hours after tracer injection.

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

13 maj 2026

Primärt slutförande (Beräknad)

1 maj 2027

Avslutad studie (Beräknad)

1 maj 2027

Studieregistreringsdatum

Först inskickad

7 maj 2026

Först inskickad som uppfyllde QC-kriterierna

6 juni 2026

Första postat (Faktisk)

10 juni 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

10 juni 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

6 juni 2026

Senast verifierad

1 maj 2026

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