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Bioavailability of Spermidine in Healthy Males

Not Applicable
Active, not recruiting
Conditions
Healthy Subjects
Registration Number
NCT06017219
Lead Sponsor
Chrysea Labs Lda
Brief Summary

To evaluate in healthy males the safety of two doses of spermidine as assessed by occurrence of any Adverse Events/Serious adverse events.

Detailed Description

Until now, lack of availability of a reproducible high quality, uncontaminated, spermidine for human consumption as a food or supplement has been a significant barrier to its study and use.

Chrysea is producing spermidine by a patented biological process to consistently produce very high purity spermidine to pharmaceutical and food grade standards.

Using a rat ex vivo jejunal absorption model and 14Carbon labelled spermidine, the recovery rate of radioactivity at the portal vein was approximately 61-76% during the initial 10 minutes after the administration of 14C-spermidine.

Data on spermidine absorption in humans is very limited. The purpose of this single blind randomised pharmacokinetic study is to demonstrate absorption of 20mg and 40 mg doses of spermidine in fasted normal volunteers, and to describe the absorption kinetics (Tmax, Cmax, T1/2, AUC).

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
Male
Target Recruitment
6
Inclusion Criteria
  • Able to give written informed consent.
  • Male.
  • Age between 18-70 years inclusive.
  • BMI between ≥18.5 and ≤28 kg/m2.
  • In general good health, as determined by the investigator.
  • Agree to abstain from consuming alcohol, grapefruit, or grapefruit juice for 72 hours prior to visit 2 and visit 3.
  • Adequate vein access for cannulation and multiple blood draws.
  • Able to communicate well with the Investigator, to understand and comply with the requirements of the study and be judged suitable for the study in the opinion of the Investigator.
  • Willing to consume the study product.
Exclusion Criteria
  • History of anaphylaxis,
  • Documented hypersensitivity reaction or a clinically important reaction to any dietary/food supplement or drug,
  • Intolerance or sensitivity to study product ingredients

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Primary Outcome Measures
NameTimeMethod
Cmax. To evaluate the pharmacokinetics of two different doses (20 mg and 40mg) of spermidine in healthy malesPre dosing to dosing plus six hours

Maximum concentration of circulating spermidine (Cmax)

AUC. To evaluate the pharmacokinetics of two different doses (20 mg and 40mg) of spermidine in healthy malesPre dosing to dosing plus six hours

Area Under the Curve (AUC)

Tmax. To evaluate the pharmacokinetics of two different doses (20 mg and 40mg) of spermidine in healthy malesPre dosing to dosing plus six hours

Time to peak of circulating spermidine (Tmax)

T 1/2. To evaluate the pharmacokinetics of two different doses (20 mg and 40mg) of spermidine in healthy males.Pre dosing to dosing plus six hours

Half-life of circulating spermidine (t1/2)

Secondary Outcome Measures
NameTimeMethod
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