Atlantia Clinical Trials, 1st Floor, Block C, Heron House, Blackpool Retail Park, Cork
Cork, Ireland
NCT Number: NCT06017219
To evaluate in healthy males the safety of two doses of spermidine as assessed by occurrence of any Adverse Events/Serious adverse events.
This study is active but is not currently recruiting participants.
Notify Me18 year–70 year
Male
Interventional
Not applicable
Cork, Ireland
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).
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
spermidine
Time frame: Pre dosing to dosing plus six hours
Maximum concentration of circulating spermidine (Cmax)
Time frame: Pre dosing to dosing plus six hours
Time to peak of circulating spermidine (Tmax)
Time frame: Pre dosing to dosing plus six hours
Half-life of circulating spermidine (t1/2)
Time frame: Pre dosing to dosing plus six hours
Area Under the Curve (AUC)
Chrysea Labs Lda
Industry
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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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