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RECRUITING NA

Nicotinamide Adenine Dinucleotide Responses to a Nutritional Supplement

NCT07428889 · View on ClinicalTrials.gov ↗

Study Summary

The objective of this study is to evaluate nicotinamide adenine dinucleotide (NAD+) in response to a proprietary nutritional supplement in generally healthy adults, compared to placebo.

Conditions Studied

Interventions

  • DIETARY_SUPPLEMENT Placebo Supplement
  • DIETARY_SUPPLEMENT Proprietary Nutritional Supplement

Study Locations (1)

Illinois

  • Biofortis Clinical Research — Addison

Trial Details

FieldValue
Enrollment Target 34 participants
Start Date 2026-02
Est. Completion 2026-06
Phase NA

Sponsor

Shaklee Corporation

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07428889

The ClinicalTrials.gov registry entry for NCT07428889 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 34 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Shaklee Corporation, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Healthy Adult appearing as the primary indexed condition, and to 2 interventions — of which Placebo Supplement is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07428889 reports 1 study location spanning 1 distinct geographic area — top geographies include Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07428889 about?

NCT07428889 is a clinical study titled "Nicotinamide Adenine Dinucleotide Responses to a Nutritional Supplement". The objective of this study is to evaluate nicotinamide adenine dinucleotide (NAD+) in response to a proprietary nutritional supplement in generally healthy adults, compared to placebo.

What is the current status of trial NCT07428889?

This trial is currently recruiting. It is a NA study. The enrollment target is 34 participants. The study started on 2026-02. Estimated completion is 2026-06.

What conditions does trial NCT07428889 study?

This clinical trial studies the following conditions: Healthy Adult. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07428889?

The interventions under investigation include: Placebo Supplement (DIETARY_SUPPLEMENT), Proprietary Nutritional Supplement (DIETARY_SUPPLEMENT). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07428889?

This trial is sponsored by Shaklee Corporation, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07428889 being conducted?

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

Related

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