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NCT04495920 · ClinicalTrials.gov registry record · Early Phase 1

Clinical Evaluation of the Residual Antimicrobial Activity

A Early Phase 1 study, sponsored by CAGE Bio.

Completed
Registry status
Early Phase 1
Development phase
12
Enrollment target

NCT04495920: Completed Early Phase 1 study, sponsored by CAGE Bio.

NCT04495920 is a Early Phase 1 study that has completed, run by CAGE Bio. The registered enrollment target is 12 participants, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04495920, a Early Phase 1 study, has completed, sponsored by CAGE Bio.

COMPLETED
Registry status
Early Phase 1
Development phase
12 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the residual antimicrobial efficacy of one test product as defined by the difference between the number of a challenge bacterial species recovered following exposure to the test product and the number recovered when untreated (negative control). The challenge bacterial species to be used is Staphylococcus aureus (ATCC #6538) (S. aureus). Testing will be carried out using a modification of the standardized test method described in ASTM E2752-10 (2015) Standard Guide for Evaluation of Residual Effectiveness of Antibacterial Personal Cleansing Products. Bacterial recoveries will be assayed after application oftest material, using the forearms as a substrate.

Interventions

  • DRUG CGB-S-100

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2020-06-16
Est. Completion 2020-07-28
Phase Early Phase 1
CAGE Bio

8 total trials

What the finished NCT04495920 record still lists

NCT04495920 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (77% lower).

The record links to 0 conditions, and to 1 intervention - of which CGB-S-100 is the first listed.

NCT04495920 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04495920 about?

NCT04495920 is a clinical study titled "Clinical Evaluation of the Residual Antimicrobial Activity". The purpose of this study is to evaluate the residual antimicrobial efficacy of one test product as defined by the difference between the number of a challenge bacterial species recovered following exposure to the test product and the number recovered when untreated (negative control). The challenge...

What is the current status of trial NCT04495920?

This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 12 participants. The study started on 2020-06-16. Estimated completion is 2020-07-28.

What interventions are being tested in trial NCT04495920?

The interventions under investigation include: CGB-S-100 (DRUG).

Who is sponsoring clinical trial NCT04495920?

This trial is sponsored by CAGE Bio, which has 8 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04495920's enrollment target sits among peer trials

12 1530th of 2000 higher than 401 of 2,000 other Early Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Early Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04495920, the US trial registry maintained by the National Library of Medicine. NCT04495920 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.