Test-retest Trial With [11C]MODAG-005 in PD or MSA and AMHC - Pilot Phase (PIOSA)
An Open-label, Single-center Study to Evaluate the Safety and Test-retest Characteristics of [11C]MODAG-005 as PET Radioligand for Imaging Pathological Alpha-synuclein Deposition in the Brains of Patients With Parkinson's Disease (PD) or Multiple System Atrophy (MSA) Compared to Age-matched Healthy Controls (AMHC) - Pilot Phase
This is an open-label, single-center Phase 1 study evaluating the safety, tolerability, and test-retest characteristics of [11C]MODAG-005, an investigational positron emission tomography/computed tomography (PET/CT) radioligand intended to image pathological alpha-synuclein deposition in the brain. The study will enroll participants with Parkinson's disease (PD), participants with multiple system atrophy (MSA), and age-matched healthy controls (AMHC).
Participants with PD or MSA will undergo two [11C]MODAG-005 PET/CT imaging sessions: one baseline scan and one follow-up scan 7 to 48 days later. Age-matched healthy controls will undergo one baseline scan. A subset of PD and MSA participants will receive a single oral dose of anle138b (Emrusolmin) before the second scan to evaluate tracer uptake under blocking conditions. The primary objective is to assess the safety and tolerability of [11C]MODAG-005. Secondary objectives include evaluating whether [11C]MODAG-005 PET imaging can distinguish participants with MSA or PD from age-matched healthy controls, distinguish PD from MSA, and determine test-retest variability of PET outcome measures.
調査の概要
詳細な説明
This is an open-label, single-center Phase 1 study evaluating [11C]MODAG-005, an investigational Positron Emission Tomography (PET) radioligand for imaging pathological alpha-synuclein deposition in the brain. The study will enroll participants with Parkinson's disease (PD), participants with multiple system atrophy (MSA), and age-matched healthy controls (AMHC).
Participants with PD or MSA will undergo two [11C]MODAG-005 PET/CT scans: a baseline scan and a follow-up scan 7 to 48 days later. Age-matched healthy controls will undergo one baseline PET/CT scan. A subset of PD and MSA participants will receive a single oral dose of 300 mg anle138b (Emrusolmin) before the second scan to evaluate tracer uptake under blocking conditions.
The primary objective is to assess the safety and tolerability of [11C]MODAG-005 based on adverse events, vital signs, physical examinations, laboratory tests, and electrocardiograms. Secondary objectives include evaluating whether [11C]MODAG-005 PET imaging can distinguish MSA from healthy controls, PD from healthy controls, and PD from MSA, and assessing test-retest variability of PET imaging measures.
Exploratory analyses will assess tracer uptake with and without anle138b blocking, blood radioactivity and metabolite profiles, image-derived input functions, visual PET reads, and relationships between PET signal and clinical measures. Total study participation will last up to 12 weeks from screening to final follow-up.
研究の種類
入学 (推定)
段階
- 初期フェーズ 1
連絡先と場所
研究連絡先
- 名前:Johannes Levin, MD
- 電話番号:+49-6734-9622-8000
- メール:levin@modag.net
研究場所
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Baden-Wurttemberg
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Tübingen、Baden-Wurttemberg、ドイツ
- 募集
- Radiologische Klinik, Universitätsklinikum Tübingen, Abt. Nuklearmedizin & Klinische Molekulare Bildgebung
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コンタクト:
- Sibylle Braun-Lukaszewitz, PhD
- 電話番号:83213 +49-7071-29-
- メール:sibylle.braun-lukaszewitz@med.uni-tuebingen.de
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主任研究者:
- Christian La Fougère, MD
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参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Key inclusion criteria: Patients with MSA fulfilling both the criteria for probable MSA (Gilman et al., 2008) and clinically established MSA (Wenning et al., 2022), patients with PD fulfilling the criteria for clinically established PD (Postuma et al., 2015) or age-matched healthy controls (AMHC).
Exclusion Criteria:
- Laboratory tests with clinically significant abnormalities and/or clinically significant unstable medical illness equivalent to CTC v5.0 (common toxicity criteria) toxicities greater than grade 2.
- Evidence of clinically significant disease that is expected to interfere with cognitive assessments or the ability to complete the trial procedures as judged by the investigator.
- Clinically significant renal and hepatic dysfunction as judged by the investigator.
- Known hypersensitivity to the active substance or to any of the excipients of [11C]MODAG-005 solution for injection.
- Known hypersensitivity to the active substance or to any of the excipients in anle138b (Emrusolmin) capsules.
- Participant has received an investigational drug within 3 months of screening.
- Blood donations within 7 days before enrolment.
- Pregnant (see 9.1.5) or breast-feeding or having the intention of getting pregnant. Female participants of childbearing potential and male participants with female partners of childbearing potential not willing to practice effective contraception during the trial period and for 90 days following each PET/CT scan.
- Unsuitable veins for repeated venipuncture.
- Contraindication to blood sampling and/or arterial cannulation, including but not limited to allergy to local anesthetics, peripheral vascular disease, Raynaud's phenomenon as determined by abnormal Allen's test on both arms or abnormal coagulation profile at screening. If Allen's test should be "abnormal" on both arms, the participant will not be eligible for arterial sampling, but will participate in the remaining assessments.
- MRI exclusion criteria include but not limited to: findings of cerebrovascular disease (more than two lacunar infarcts, any territorial infarct >1 cm^3, or deep white matter abnormality corresponding to an overall Fazekas scale of 3 with at least one confluent hyperintense lesion on the Fluid-Attenuated Inversion Recov ery (FLAIR) sequence that is >20 mm in any dimension), infectious disease, space-occupying lesions normal pressure hydrocephalus or any other abnormalities associated with central nervous system (CNS) disease. Findings that are expected to be present in the PD and MSA participants (e.g. absence of swallow tail sign, presence of regional atrophy or hot cross bun sign) do not lead to exclusion of these participants.
- Implants such as implanted cardiac pacemakers or defibrillators, insulin pumps, cochlear implants, metallic ocular foreign body, implanted neural stimulators, CNS aneurysm clips and other medical implants that have not been certified for MRI, or history of claustrophobia in MRI.
Unwilling and/or unable to cooperate with trial procedures.
Exclusion criteria for age-matched healthy controls:
- Relevant hepatic parameters above upper limit of normal (ULN), i.e., glutamic pyruvic transaminase (GPT), glutamic oxaloacetic transaminase (GOT), bilirubin
- Relevant renal parameters outside normal limits, i.e., serum creatinine and blood urea nitrogen (BUN) above ULN; urinary albumin-creatinine ratio (uACR) below lower limit of normal (LLN)
- Systolic blood pressure <90 or >140 mmHg; diastolic blood pressure <45 or >90 mmHg; heart rate <50 or >95 beats per minute (BPM)
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:診断
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的:Parkinson´s Disease (PD), Multiple System Atrophy (MSA), Healthy controls (HC)
Each participant with PD and each participant with MSA will receive two injections of up to 18 mL of [11C]MODAG-005 solution for injection with 40 - 400 MBq within 12 weeks.
Each HC will receive one injection of up to 18 mL of [11C]MODAG-005 solution for injection with 40 - 400 MBq.
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Injection of [11C]MODAG-005 followed by PET imaging.
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Safety and Tolerability
時間枠:Inclusion to 4 days (± 2 days) post injection.
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AEs related to the medication
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Inclusion to 4 days (± 2 days) post injection.
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|
Safety and tolerability
時間枠:Inclusion to 4 days (± 2 days) post injection.
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AEs leading to discontinuation/drop-out rates
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Inclusion to 4 days (± 2 days) post injection.
|
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Safety and tolerability
時間枠:Inclusion to 4 days (± 2 days) post injection.
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SAEs related to the study medication.
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Inclusion to 4 days (± 2 days) post injection.
|
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Safety and tolerability
時間枠:Inclusion to 4 days (± 2 days) post injection.
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Change in vital signs (heart rate [Hz], blood pressure [mmHg], body temperature[°C]) secondary to injection with [11C]MODAG-005.
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Inclusion to 4 days (± 2 days) post injection.
|
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Safety and tolerability
時間枠:Inclusion to 4 days (± 2 days) post injection.
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Change in physical examination findings secondary to injection with [11C]MODAG-005.
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Inclusion to 4 days (± 2 days) post injection.
|
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Safety and tolerability
時間枠:Inclusion to 4 days (± 2 days) post injection.
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Change in clinical laboratory results including hematology and clinical chemistry including renal function tests, hepatic enzymes, electrolytes and creatine kinase secondary to injection with [11C]MODAG-005.
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Inclusion to 4 days (± 2 days) post injection.
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Safety and tolerability
時間枠:Inclusion to 4 days (± 2 days) post injection.
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Cahnge in 12-lead ECG parameters including QT interval corrected for heart rate using Fridericia's formula (QTcF) secondary to injection with [11C]MODAG-005
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Inclusion to 4 days (± 2 days) post injection.
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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To assess the ability of [11C]MODAG-005 to discriminate between MSA and HC.
時間枠:Slots between 0 and 90 minutes after tracer injection.
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Standardized uptake value ratio (SUVR) for different imaging time windows, volume of distribution (VT) and distribution volume ratio (DVR) in different brain regions between participants with MSA and AMHC from PET acquisitions after administration of [11C]MODAG-005.
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Slots between 0 and 90 minutes after tracer injection.
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To assess the ability of [11C]MODAG-005 to discriminate between PD and HC
時間枠:Slots between 0 and 90 minutes after tracer injection.
|
SUVR for different imaging time windows, VT, and DVRin different brain regions between patients with PD and AMHC from PET acquisitions after administration of [11C]MODAG-005.
|
Slots between 0 and 90 minutes after tracer injection.
|
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To assess the ability of [11C]MODAG-005 to discriminate between PD and MSA
時間枠:Slots between 0 and 90 minutes after tracer injection.
|
SUVR for different imaging time windows, VT, and DVR in different brain regions between participants with PD and participants with MSA from PET acquisitions after administration of [11C]MODAG-005.
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Slots between 0 and 90 minutes after tracer injection.
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To determine test-retest variability in PD and MSA under blocking conditions.
時間枠:8-49 days after first tracer injection.
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Test-retest variability of SUVR for different time imaging time windows and DVR after administration of [11C]MODAG-005 in PD and MSA under blocking with a single dose of Emrusolmin 300 mg.
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8-49 days after first tracer injection.
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協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
キーワード
追加の関連 MeSH 用語
その他の研究ID番号
- MODAG-005-P1-01
- 2023-506965-72-00 (Ctis)
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