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Study on the relative bioavailability of liposome ß - nicotinamide mononucleotide

Study on the relative bioavailability of liposome ß - nicotinamide mononucleotide

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096819
Enrollment
Unknown
Registered
2025-02-07
Start date
2025-04-30
Completion date
Unknown
Last updated
2025-02-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Relative bioavailability

Interventions

R-T group:Test sample A is taken in the first cycle, and after a washout period of 5-12 days, test sample B is taken in the second cycle
Sample A is one of liposomes ß nicotinamide mononucleotide and common ß nicotinamide mononucleotide, and sample B is another of liposome ß nicotinamide mononucleotide and ß ordinary nicotinamide monon
T-R group:Test sample B is taken in the first cycle, and after a washout period of 5-12 days, test sample A is taken in the second cycle

Sponsors

The First People's Hospital of Kunshan
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Male aged 18 - 45 years old (including boundary value); 2. Body mass index (BMI) 19.0 kg/m^2 – 28.0 kg/m^2 (including cut-off value); 3. Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Those with serious diseases of the heart, liver, kidney, and hematopoietic system, and patients with mental illness; 2. Those with hypoglycemia; 3. Those who need to take drugs during the trial; 4. Those who have suffered from clinically significant major diseases or undergone major surgical operations within 3 months before screening, or those who plan to undergo surgery during the study period; 5. Those who are addicted to alcohol or those who cannot abstain from alcohol during the test; 6. Smokers or those who cannot stop smoking during the test; 7. Those who have used any drugs (including prescription drugs, over-the-counter drugs, traditional Chinese medicines, etc.) within 2 weeks before screening; 8. Those who cannot tolerate venipuncture or have a history of fainting blood or needle sickness; 9. Those who have a history of drug abuse or have used drugs; 10. Poor compliance in the opinion of the investigator, or any other situation in the opinion of the investigator that the subject is not suitable to participate in this trial.

Design outcomes

Primary

MeasureTime frame
ß - nicotinamide mononucleotide;Maximum blood concentration;Area under the curve;

Secondary

MeasureTime frame
Peak time;Half-life;

Countries

China

Contacts

Public ContactChen Yafang

The First People's Hospital of Kunshan

147301945@qq.com+86 137 7171 5540

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026