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Investigation for efficacy and safety of [18F] SPAL-T-06

Investigation for efficacy and safety of alpha-synuclein PET ligand [18F] SPAL-T-06

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs031210180
Enrollment
30
Registered
2021-07-02
Start date
2021-07-29
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dementia with Lewy bodies, Parkinson's disease, and multiple system atrophy

Interventions

Injection of [18F]SPAL-T-06 and PET scan

Sponsors

Endo Hironobu
Lead Sponsor
Higuchi Makoto
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (A) Brain dynamics evaluation Patients (6 patients with dementia with Lewy bodies, 6 patients with Parkinson's disease, and 6 patients with multiple system atrophy) (1) Patients who are 20 years old or older at the time of consent acquisition. (2) Patients whom a potential substitute can accompany on the day of participation in the study at NIRS. (3) Patients with dementia with Lewy bodies and Parkinson's disease: Patients who meet the UK Parkinson's disease society brain bank clinical diagnostic criteria or the diagnostic criteria of McKeith et al. (4) Patients with multiple system atrophy: Patients who meet Gilman's clinical diagnosis criteria for MSA. Healthy subjects (6 Healthy subjects) (1) Healthy adults who have been determined to be eligible for this study by the principal investigator or sub-investigator. (2) Those who are 20 years of age or older at the time of obtaining consent. (B) Whole body dynamic evaluation (6 Healthy subjects; 3 male and 3 female) (1) Healthy adults who are judged to be eligible for this study by a medical examination by the principal investigator or sub-investigator. (2) Healthy adults who are 50 years of age or older at the time consent is obtained.

Exclusion criteria

Exclusion criteria: (1) Patients with a history of or complications from organic brain disease (for example, disorders of consciousness, head trauma requiring hospitalization, evident cerebral infarction, or cerebral hemorrhage). (2) Patients with substance-related disorders (for example, drug dependence). (3) Those who have complications from serious diseases or those who have a history of such diseases, judged by the principal investigator or sub-investigator to be inappropriate for this study. (4) Those who have magnetic metals in their body (for example, tattoos, tattoos including art makeup, pacemakers) (for brain dynamics evaluation only). (5) Persons with intense claustrophobia. (6) Those who are pregnant or may be pregnant, and those who are breast-feeding. (7) Those who are allergic to local anesthetics and blood coagulation inhibitors. (Brain dynamics evaluation only) (8) Those who are taking the anticoagulant medication. (Brain dynamics evaluation only) (9) Others judged by the principal investigator or sub-investigator to be inappropriate as research subjects.

Design outcomes

Primary

MeasureTime frame
(A) Brain dynamics evaluation Efficacy evaluation: Quantitative evaluation of the brain dynamics of [18F] SPAL-T-06 and the extent and distribution of alpha-synuclein lesions in patients with dementia with Lewy bodies, Parkinson's disease, multiple system atrophy, and healthy volunteers. Safety evaluation: Changes in subjective symptoms, other findings, and laboratory tests after [18F] SPAL-T-06 administration. (B) Whole body dynamic evaluation Efficacy evaluation: Distribution test of [18F] SPAL-T-06 in the whole body. Safety evaluation: Effective dose per unit dose of radiation of [18F] SPAL-T-06. Changes in subjective symptoms, other findings, and laboratory tests after [18F] SPAL-T-06 administration.

Secondary

MeasureTime frame
(A) Brain dynamics evaluation In patients with dementia with Lewy bodies, Parkinson's disease, multiple system atrophy, and healthy volunteers, we will explore the relationship between (1) the extent and distribution of alpha-synuclein lesions assessed by PET using [18F] SPAL-T-06, (2) abnormal protein accumulation in the brain assessed by PET using [11C]PiB (2) Brain accumulation of abnormal proteins assessed by PET using [11C]PiB, (3) Brain structure and neurotransmission function assessed by MRI data, (4) Correlation between blood data and clinical symptom scores. (2)-(4) will also be evaluated using existing data.

Contacts

Public ContactHironobu Endo

National Institutes for Quantum Science and Technology

endo.hironobu@qst.go.jp+81-43-206-3251

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026