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Efficacy and safety of [11C]NCGG401

Efficacy and safety of [11C]NCGG401 as a PET imaging ligand for microglia in the brain

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs031210249
Enrollment
9
Registered
2021-08-18
Start date
2021-12-08
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

Alzheimers disease

Interventions

Injection of [11C]NCGG401 and PET scans

Sponsors

Kimura Yasuyuki
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1) Males who are between 20 and 40 years old at the time of consent. 2) A person who voluntarily applies for the study and is judged by the principal investigator or sub-investigator to be able to understand the contents of the explanatory document.

Exclusion criteria

Exclusion criteria: 1) Patients with obvious abnormality in the clinical examination conducted after obtaining consent. 2) Patients whose head MRI scan revealed findings that are suspected to affect the PET scan (such as a clear history of cerebral infarction or cerebral hemorrhage). 3)Those whose cognitive or intellectual functioning is below the normal range on psychological testing, and those whose developmental or mental status is considered to interfere with testing (Step 2 only). 4) Those who have magnetic metals in their body (tattoos, tattoos including art makeup, pacemakers, etc.). 5) Those who are highly claustrophobic. 6) Those who have a history of drug allergy. 7) Those who have serious complications or those who have a history of such complications and are judged by the principal investigator or sub-investigator to be ineligible for this study. 8) Subjects who are regularly taking steroidal or non-steroidal anti-inflammatory drugs. 9) Those who have participated in other clinical research involving intervention for less than one year from the time of obtaining consent. 10) Those who have participated in nuclear medicine examinations of other healthy volunteers for less than 6 months from the time of obtaining consent, in view of radiation exposure in nuclear medicine examinations. 11) Those who have not consented to the storage of specimens in our biobank. 12) Any other person who is judged by the principal investigator or sub-investigator to be ineligible as a subject of this study.

Design outcomes

Primary

MeasureTime frame
Clinical Safety of [11C]NCGG401 Injection Systemic kinetics of [11C]NCGG401 Accuracy of Measurement of Volume of Distribution of [11C]NCGG401

Secondary

MeasureTime frame
Effective dose per unit dose of radiation for [11C]NCGG401 injection solution Correlation between volume of distribution of [11C]NCGG401 and volume of distribution of [11C]DPA-713 Correlation between volume of distribution of [11C]NCGG401 and blood markers. Effect of single nucleotide polymorphism of CSF1R on the volume of distribution of [11C]NCGG401

Contacts

Public ContactYasuyuki Kimura

National Center for Geriatrics and Gerontology

yazkim@ncgg.go.jp+81-562-46-2311

Outcome results

None listed

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