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Phase 1 Clinical Study of JTC-064 -Multiple Dose Study-

Phase 1 Clinical Study of JTC-064 -Multiple Dose Study-

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2071250054
Enrollment
36
Registered
2025-07-28
Start date
2025-08-25
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

Neurodegenerative disease

Interventions

JTC-064 or placebo will be administered orally once daily for 28 days.

Sponsors

Yamane Satoshi
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Healthy Japanese male aged from 18 to 45 years (inclusive) at informed consent 2. A subject with a body mass index of 18.5 to less than 25.0 at the screening visit

Exclusion criteria

Exclusion criteria: 1. A subject who has serious medical history of or complications under treatment for the cerebral, liver, kidneys, heart, lungs, gastrointestinal system, hematological, endocrine system, metabolic system, or psychiatric disorders. 2. A subjcet who has a history of gastrointestinal surgery that could interfere with the absorption of the study drug. 3. A subject who has participated in this study and received the study drug administration. 4. A subject who, in the opinion of the Investigator, has impediments to participation in the study.

Design outcomes

Primary

MeasureTime frame
Safety, Pharmacokinetics

Contacts

Public Contactinformation clinical trials

Shionogi & Co.,Ltd.

clinicaltrials-info@shionogi.co.jp+81-3-6635-3505

Outcome results

None listed

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