- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07640555
Evaluation of [¹⁸F]MODAG-009 PET Imaging in Synucleinopathies (MODAG-009-P1-0)
Studienübersicht
Status
Intervention / Behandlung
Detaillierte Beschreibung
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.
Studientyp
Einschreibung (Geschätzt)
Phase
- Frühphase 1
Kontakte und Standorte
Studienkontakt
- Name: Johannes Levin, MD
- Telefonnummer: 475-318-8250 (24 hours)
- E-Mail: Levin@modag.net
Studienorte
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Connecticut
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New Haven, Connecticut, Vereinigte Staaten, 06510
- Rekrutierung
- Institute for Neurodegenerative Disorders and XingImaging, LLC
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Hauptermittler:
- Neha Prakash, MBBS
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Kontakt:
- Mackenzee George
- Telefonnummer: 475-318-8250 (24 hours)
- E-Mail: mgeorge@xingimaging.com
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-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria:
Healthy Controls inclusion criteria:
- Enrolled in the PPMI 002 Clinical study as a healthy control participant
- Any gender aged 50 to 75 years of age
- Negative CSF α-synuclein seed amplification assay (SAA)
- Previously acquired (since inclusion in PPMI) brain MRI without evidence of significant neurological pathology.
- 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.
- 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:
- Enrolled in the PPMI 002 Clinical study as a Parkinson's Disease (PD) or Prodromal participant
- Any gender aged 50 to 80 years of age
- Positive CSF SAA
- 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.
- 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:
- Any gender aged 50 to 75 years of age
- 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)
- Positive CSF SAA
- 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.
- 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:
- Clinical evidence of other neurodegenerative diseases, such as Alzheimer's disease
- Any other medical or psychiatric condition or lab abnormality, which in the opinion of the investigator might preclude participation.
- Received any of the following drugs: dopamine receptor blockers (neuroleptics), metoclopramide, lithium and reserpine, within 6 months of Baseline Visit.
- 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.
- Participation in an investigational drug trial targeting α-synuclein within the past 6 months prior to enrollment.
- 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.
- 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.
- 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.
- 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.
- 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.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Diagnose
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: 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.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Standard Uptake Value Ratios (SUVR)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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.
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Safety, tolerability, and feasibility
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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.
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From baseline to follow-up 2-3 business days after tracer injection.
|
|
Safety, tolerability, and feasibility
Zeitfenster: 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.
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From baseline to follow-up 2-3 business days after tracer injection.
|
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Safety, tolerability, and feasibility
Zeitfenster: 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.
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From baseline to follow-up 2-3 business days after tracer injection.
|
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Safety, tolerability, and feasibility
Zeitfenster: 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.
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From baseline to follow-up 2-3 business days after tracer injection.
|
|
Safety, tolerability, and feasibility
Zeitfenster: 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.
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From baseline to follow-up 2-3 business days after tracer injection.
|
|
Safety, tolerability, and feasibility
Zeitfenster: 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
Zeitfenster: 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.
|
Mitarbeiter und Ermittler
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Synucleinopathien
- Erkrankungen des Gehirns
- Erkrankungen des zentralen Nervensystems
- Erkrankungen des Nervensystems
- Neurodegenerative Krankheiten
- Bewegungsstörungen
- Parkinsonsche Störungen
- Erkrankungen der Basalganglien
- Primäre Dysautonomien
- Erkrankungen des autonomen Nervensystems
- Parkinson Krankheit
- Multiple Systematrophie
Andere Studien-ID-Nummern
- MODAG-009-P1-01
Plan für individuelle Teilnehmerdaten (IPD)
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Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
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