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

6. juni 2026 opdateret af: 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.

Studieoversigt

Detaljeret beskrivelse

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.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

13

Fase

  • Tidlig fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

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

Studiesteder

    • Connecticut
      • New Haven, Connecticut, Forenede Stater, 06510
        • Rekruttering
        • Institute for Neurodegenerative Disorders and XingImaging, LLC
        • Ledende efterforsker:
          • Neha Prakash, MBBS
        • Kontakt:

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ja

Beskrivelse

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

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Diagnostisk
  • Tildeling: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: 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.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Standard Uptake Value Ratios (SUVR)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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.

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Safety, tolerability, and feasibility
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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.

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

13. maj 2026

Primær færdiggørelse (Anslået)

1. maj 2027

Studieafslutning (Anslået)

1. maj 2027

Datoer for studieregistrering

Først indsendt

7. maj 2026

Først indsendt, der opfyldte QC-kriterier

6. juni 2026

Først opslået (Faktiske)

10. juni 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

10. juni 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

6. juni 2026

Sidst verificeret

1. maj 2026

Mere information

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UBESLUTET

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Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ja

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

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