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

2026년 6월 6일 업데이트: 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.

연구 개요

상세 설명

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.

연구 유형

중재적

등록 (추정된)

13

단계

  • 초기 1단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

  • 이름: Johannes Levin, MD
  • 전화번호: 475-318-8250 (24 hours)
  • 이메일: Levin@modag.net

연구 장소

    • Connecticut
      • New Haven, Connecticut, 미국, 06510
        • 모병
        • Institute for Neurodegenerative Disorders and XingImaging, LLC
        • 수석 연구원:
          • Neha Prakash, MBBS
        • 연락하다:

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 특수 증상
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 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.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Standard Uptake Value Ratios (SUVR)
기간: 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)
기간: 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)
기간: 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.

2차 결과 측정

결과 측정
측정값 설명
기간
Safety, tolerability, and feasibility
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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.

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2026년 5월 13일

기본 완료 (추정된)

2027년 5월 1일

연구 완료 (추정된)

2027년 5월 1일

연구 등록 날짜

최초 제출

2026년 5월 7일

QC 기준을 충족하는 최초 제출

2026년 6월 6일

처음 게시됨 (실제)

2026년 6월 10일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 6월 10일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 6월 6일

마지막으로 확인됨

2026년 5월 1일

추가 정보

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미정

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아니

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파킨슨병에 대한 임상 시험

[¹⁸F]MODAG-009 PET imaging에 대한 임상 시험

구독하다