Evaluation of [¹⁸F]MODAG-009 PET Imaging in Synucleinopathies (MODAG-009-P1-0)
Přehled studie
Postavení
Postavení
Podmínky
Podmínky
Intervence / Léčba
Intervence / Léčba
Detailní popis
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.
Typ studie
Typ studie
Zápis (Odhadovaný)
Zápis
Fáze
Fáze
- Raná fáze 1
Kontakty a umístění
Studijní kontakt
Studijní kontakt
- Jméno: Johannes Levin, MD
- Telefonní číslo: 475-318-8250 (24 hours)
- E-mail: Levin@modag.net
Studijní místa
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Connecticut
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New Haven, Connecticut, Spojené státy, 06510
- Nábor
- Institute for Neurodegenerative Disorders and XingImaging, LLC
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Vrchní vyšetřovatel:
- Neha Prakash, MBBS
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Kontakt:
- Mackenzee George
- Telefonní číslo: 475-318-8250 (24 hours)
- E-mail: mgeorge@xingimaging.com
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Kritéria účasti
Kritéria způsobilosti
Kritéria způsobilosti
Věk způsobilý ke studiu
- Dospělý
- Starší dospělý
Přijímá zdravé dobrovolníky
Popis
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.
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Diagnostický
- Přidělení: N/A
- Intervenční model: Přiřazení jedné skupiny
- Maskování: Žádné (otevřený štítek)
Počet zbraní
Zbraně a zásahy
Skupina účastníků / ArmSkupina účastníků / Arm |
Intervence / LéčbaIntervence / Léčba |
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Experimentální: 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.
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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.
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Co je měření studie?
Primární výstupní opatření
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Standard Uptake Value Ratios (SUVR)
Časové okno: Up to 3 hours after tracer injection.
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To evaluate Standard Uptake Value Ratios (SUVR) in brain regions from [18F]MODAG-009 in participants with PD.
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Up to 3 hours after tracer injection.
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Standard Uptake Value Ratios (SUVR)
Časové okno: Up to 3 hours after tracer injection.
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To evaluate Standard Uptake Value Ratios (SUVR) in brain regions from [18F]MODAG-009 in participants with MSA.
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Up to 3 hours after tracer injection.
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Standard Uptake Value Ratios (SUVR)
Časové okno: Up to 3 hours after tracer injection.
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To evaluate Standard Uptake Value Ratios (SUVR) in brain regions from [18F]MODAG-009 in HC participants.
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Up to 3 hours after tracer injection.
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Sekundární výstupní opatření
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Safety, tolerability, and feasibility
Časové okno: From baseline to follow-up 2-3 business days after tracer injection.
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To assess the number and severity of adverse events 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
Časové okno: From baseline to follow-up 2-3 business days after tracer injection.
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To assess blood pressure [mmHg] 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
Časové okno: From baseline to follow-up 2-3 business days after tracer injection.
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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.
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Safety, tolerability, and feasibility
Časové okno: From baseline to follow-up 2-3 business days after tracer injection.
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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
Časové okno: From baseline to follow-up 2-3 business days after tracer injection.
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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
Časové okno: From baseline to follow-up 2-3 business days after tracer injection.
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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.
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Safety, tolerability, and feasibility
Časové okno: From baseline to follow-up 2-3 business days after tracer injection.
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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.
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Safety, tolerability, and feasibility
Časové okno: From baseline to follow-up 2-3 business days after tracer injection.
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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.
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From baseline to follow-up 2-3 business days after tracer injection.
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Regional brain uptake
Časové okno: Up to 3 hours after tracer injection.
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To determine regional brain uptake of [¹⁸F]MODAG-009 and binding patterns associated with α-synuclein pathology.
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Up to 3 hours after tracer injection.
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Spolupracovníci a vyšetřovatelé
Sponzor
Sponzor
Spolupracovníci
Spolupracovníci
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia (Aktuální)
Začátek studia
Primární dokončení (Odhadovaný)
Primární dokončení
Dokončení studie (Odhadovaný)
Dokončení studie
Termíny zápisu do studia
První předloženo
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Aktuální)
První zveřejněno
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Poslední zveřejněná aktualizace
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Naposledy ověřeno
Více informací
Termíny související s touto studií
Klíčová slova
Další relevantní podmínky MeSH
- Synukleinopatie
- Onemocnění mozku
- Onemocnění centrálního nervového systému
- Nemoci nervového systému
- Neurodegenerativní onemocnění
- Poruchy pohybu
- Parkinsonské poruchy
- Bazální gangliové choroby
- Primární dysautonomie
- Onemocnění autonomního nervového systému
- Parkinsonova choroba
- Mnohonásobná systémová atrofie
Další identifikační čísla studie
Další identifikační čísla studie
- MODAG-009-P1-01
Plán pro data jednotlivých účastníků (IPD)
Plánujete sdílet data jednotlivých účastníků (IPD)?
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Studuje produkt zařízení regulovaný americkým úřadem FDA
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