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Pharmacokinetic profile of ingested liver extracts in healthy volunteers.

Pharmacokinetic profile of ingested liver extracts in healthy volunteers. - Pharmacokinetic profile of ingested liver extracts in healthy volunteers.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000027705
Enrollment
6
Registered
2018-06-01
Start date
2017-06-14
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

None listed

Interventions

Single ingestion of unblinded liver extracts

Sponsors

Medical Corporation Hokubukai Utsukushigaoka Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: (1)Healthy Japanese males from 20 to 39 years of age when consented. (2)Subjects whose height is 180 cm or less and BMI is 20.0 - 24.9 kg/m2. (3)Subjects available at every designated hospital visit. (4)Subjects who agree to participate in this study and can put signature and date to informed consent form by themselves prior to the study.

Exclusion criteria

Exclusion criteria: (1)Subjects with hepatic, renal, cardiac or organ disorders, diabetes, or other serious diseases. (2)Subjects with a surgical history of digestive system (except appendicectomy). (3)Subjects with medication, or with exercise or dietary counselling by physician. (4)Subjects who cannot tolerate repetitive blood drawings. (5)Subjects who are participating in other clinical trial. (6)Subjects who have experienced a feeling of unwellness or bad physical condition by blood drawing. (7)Subjects judged as unsuitable for the study by the principal investigator for other reasons.

Design outcomes

Primary

MeasureTime frame
Concentrations of peptides in the serum.

Secondary

MeasureTime frame
Safety evaluation including subjective symptoms, examination by a physician in charge.

Countries

Japan

Contacts

Public ContactRyota Wakimoto

Medical Corporation Hokubukai Utsukushigaoka Hospital Clinical Pharmacology Center

wakimoto@ughp-cpc.jp011-882-0111

Outcome results

None listed

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