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Pharmacokinetics of active ingredients by the intake of the functional food in healthy subjects

Pharmacokinetics of active ingredients by the intake of the functional food in healthy subjects - Pharmacokinetics of active ingredients by the intake of the functional food

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000019387
Enrollment
6
Registered
2016-10-27
Start date
2015-10-19
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 adult subjects

Interventions

Single ingestion of the functional food

Sponsors

TTC Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Healthy adult males from 20 to 50 years of age

Exclusion criteria

Exclusion criteria: (1) Those who are gastrointestinal diseases and history (except the appendicitis) (2) Those who are judged as inappropriate for the study based on the results of clinical examination and cardiopulmonary function by the investigator (3) Those who have diseases such as diabetes, a liver disease, kidney disease, gastrointestinal disease, serious heart disease, skin disease, and diseases affecting the secretion of sex disease in the past or present, or have history (4) Those who take the prescription drug (including external medicine) (5) Those who might be liable to allergy related to the study (ex. food allergy) (6) Those who participates in other clinical study at the start of the study or are planned to participate in other clinical study during the study (7) Those who exceed donation criteria of the Japanese Red Cross within one year from the date of informed consent for the study (8) Those who are judged as unsuitable for the study based on the results of body measurements, physical and clinical examination on preliminary examination (9) Those who are judged as unsuitable for the study based on the results of lifestyle questionnaire (10) Those who has been determined to be inappropriate of the study by the investigator

Design outcomes

Primary

MeasureTime frame
Cmax, Tmax

Countries

Japan

Contacts

Public ContactShingo Yamamichi

TTC Co., Ltd Clinical Research Planning Department

s.yamamichi@ttc-tokyo.co.jp03-5459-5329

Outcome results

None listed

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