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Active, Not Recruiting

NCT Number: NCT06017219

Bioavailability of Spermidine in Healthy Males

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

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Conditions

Age range

18 year–70 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Atlantia Clinical Trials, 1st Floor, Block C, Heron House, Blackpool Retail Park, Cork

Cork, Ireland

About this study

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).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Spermidine

Dietary Supplement

spermidine

Primary outcomes

  1. Cmax. To evaluate the pharmacokinetics of two different doses (20 mg and 40mg) of spermidine in healthy males

    Time frame: Pre dosing to dosing plus six hours

    Maximum concentration of circulating spermidine (Cmax)

  2. Tmax. To evaluate the pharmacokinetics of two different doses (20 mg and 40mg) of spermidine in healthy males

    Time frame: Pre dosing to dosing plus six hours

    Time to peak of circulating spermidine (Tmax)

  3. T 1/2. To evaluate the pharmacokinetics of two different doses (20 mg and 40mg) of spermidine in healthy males.

    Time frame: Pre dosing to dosing plus six hours

    Half-life of circulating spermidine (t1/2)

  4. AUC. To evaluate the pharmacokinetics of two different doses (20 mg and 40mg) of spermidine in healthy males

    Time frame: Pre dosing to dosing plus six hours

    Area Under the Curve (AUC)

Sponsors and collaborators

Lead sponsor

Chrysea Labs Lda

Industry

Registry information

Important dates

Study start
2023
Primary completion
2023
Study completion
2024
First posted
Aug 30, 2023
Registry last updated
Aug 30, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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