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Investigation of the pharmacokinetics following oral administration of the test food

Investigation of the pharmacokinetics following oral administration of the test food - Investigation of the pharmacokinetics following oral administration of the test food

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000060946
Enrollment
5
Registered
2026-03-16
Start date
2026-03-16
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

Healthy Japanese

Interventions

Sponsors

Pharma Foods International Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Japanese 2.Men or women 3.Adults 4.Healthy individuals

Exclusion criteria

Exclusion criteria: 1.Individuals who are undergoing medical treatment or have a medical history of malignant tumor, heart failure, or myocardial infarction 2.Individuals who have a pacemaker or an implantable cardioverter defibrillator (ICD) 3.Individuals who are currently undergoing treatment for any of the following chronic diseases: cardiac arrhythmia, liver disorder, chronic kidney disease, cerebrovascular disorder, rheumatic disease, diabetes mellitus, dyslipidemia, hypertension, metabolic bone disorders, including osteoporosis and fractures, or any other chronic diseases 4.Individuals who are taking medications that affect the gastrointestinal system (including Kampo medicines) and/or supplements containing peptides or amino acids 5.Individuals who are allergic to medicines or foods related to the test product, particularly those allergic to eggs 6.Individuals whose BMI is less than 18.5 kg/m2 or 30 kg/m2 or more 7.Individuals who are undergoing exercise or alimentary therapy under medical supervision 8.Individuals who have a present condition or have a medical history of drug or alcohol dependence 9.Individuals who are undergoing treatment for psychiatric disorder (including depressive symptoms) or sleep disorder 10.Individuals who are pregnant, lactating, or planning to become pregnant during this study 11.Individuals who have been enrolled in other clinical studies within the last 28 days before the agreement to participate in this study or plan to participate in another study during this study 12.Individuals who are judged as ineligible to participate in this study by the physician

Design outcomes

Primary

MeasureTime frame
Qualitative analysis of low-molecular-weight compounds transferred into the bloodstream following the intervention

Secondary

MeasureTime frame
Quantitative analysis of low-molecular-weight compounds transferred into the bloodstream following the intervention, Proteome analysis(Comprehensive protein analysis), Metabolomic analysis(Comprehensive analysis of metabolites)

Countries

Japan

Contacts

Public ContactSaki Shirako

Pharma Foods International Co., Ltd. R&D Department

saki-shirako@pharmafoods.co.jp075-748-9829

Outcome results

None listed

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