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NCT05459961 · ClinicalTrials.gov registry record · NA

Metabolic Responses to Spermidine Supplementation.

A NA study of Healthy Subjects, sponsored by Chrysea Labs Lda.

Active
Registry status
NA
Development phase
42
Enrollment target
1
Study location

NCT05459961 is a NA study of Healthy Subjects that is active but no longer recruiting, run by Chrysea Labs Lda. The registered enrollment target is 42 participants, below the 128-participant average among 69 other Healthy Subjects trials with a reported enrollment target (67% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05459961, a NA study of Healthy Subjects, is active but no longer recruiting, sponsored by Chrysea Labs Lda.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
42 participants
Enrollment target
1
Study location

Study Summary

Spermidine is naturally present in cells, organs, circulating cardiovascular system, and as part of our normal dietary intake. Studies suggest Spermidine is involved in antioxidation, autophagy, apoptosis, and immune regulation. Spermidine is typically present in foods of plant origin, such as natto, beans, fruits, vegetables, cheese, potatoes, bread, and cereals. Adequate spermidine dietary intake is important, given evidence of declining spermidine levels with age in humans and other species, and the evidence for positive effects of spermidine supplementation on age related biology. To date, human research studies utilised extracts containing low levels of spermidine (\< 10%) and multiple other constituents, but this study will use pure spermidine to explore relevant mechanisms of action, biological effects, and identify potential biomarkers of positive biological effects.

Conditions Studied

Interventions

  • DIETARY_SUPPLEMENT oral spermidine

Study Locations (1)

Illinois

  • Biofortis Innovation Services - Addison

Trial Details

FieldValue
Enrollment Target 42 participants
Start Date 2022-08-14
Est. Completion 2025-02
Phase NA

Sponsor

Chrysea Labs Lda

1 total trials

What the Registry Record Tells You About NCT05459961

The ClinicalTrials.gov registry entry for NCT05459961 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 42 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 128-participant average among 69 other Healthy Subjects trials with a reported enrollment target (67% lower). The listed sponsor is Chrysea Labs Lda, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Healthy Subjects appearing as the primary indexed condition, and to 1 intervention - of which oral spermidine is the first listed.

NCT05459961 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.

Frequently Asked Questions

What is clinical trial NCT05459961 about?

NCT05459961 is a clinical study titled "Metabolic Responses to Spermidine Supplementation.". Spermidine is naturally present in cells, organs, circulating cardiovascular system, and as part of our normal dietary intake. Studies suggest Spermidine is involved in antioxidation, autophagy, apoptosis, and immune regulation. Spermidine is typically present in foods of plant origin, such as natto...

What is the current status of trial NCT05459961?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 42 participants. The study started on 2022-08-14. Estimated completion is 2025-02.

What conditions does trial NCT05459961 study?

This clinical trial studies the following conditions: Healthy Subjects.

What interventions are being tested in trial NCT05459961?

The interventions under investigation include: oral spermidine (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT05459961?

This trial is sponsored by Chrysea Labs Lda, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05459961 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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