None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Males and females aged 30 to 49 at resistration. 2)Subjects giving written informed consent.
Exclusion criteria
Exclusion criteria: 1) Subjects who constantly use medicines, supplements having a possibility of affecting test results. 2) Subjects who have previous and/or current medical history of serious disease such a the heart, liver, kidneys, gastrointestinal tract, etc. 3) Subjects who excessive alcohol intake. 4) Subjects who excess smoker. 5) Subjects who have extremely irregular dining habits, and subjects who have midnight work or irregular shift work. 6) Subjects who have previous medical history of drug and/or food (especially gelatin) allergy. 7) Subjects who are participating the other clinical tests. Subjects who participated within 4-weeks prior to the current study and/or who plan to participate the other clinical tests. 8) Subjects who donated over 200mL blood and/or blood components within the last one month to the current study. 9) Males who donated over 400mL blood and/or blood components within the last three month to the current study. 10)Males who will be collected over 1200mL blood and/or blood components, when the sampling amounts within the last twelve month are adding to the planned sampling amounts of this study. 11) Subjects who are positive for infectious. 12) Others who have been determined ineligible by principal investigator or sub-investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| blood IgA blood IgG | — |
Secondary
| Measure | Time frame |
|---|---|
| NK cell activity | — |
Countries
Japan
Contacts
CPCC Company Limited Sales & Planning Department