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NCT00614731 · ClinicalTrials.gov registry record · Phase 1

Responses to Immunization With Keyhole Limpet Hemocyanin Administered by Scarification and the Intradermal Route

A Phase 1 study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

Completed
Registry status
Phase 1
Development phase
25
Enrollment target

NCT00614731: Completed Phase 1 study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

NCT00614731 is a Phase 1 study that has completed, run by National Institute of Allergy and Infectious Diseases (NIAID). The registered enrollment target is 25 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (58% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00614731, a Phase 1 study, has completed, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

COMPLETED
Registry status
Phase 1
Development phase
25 participants
Enrollment target

Study Summary

Atopic dermatitis (AD) is a skin disorder in which people often have swelling and skin infections. People with this disease cannot receive the smallpox vaccine because it could cause them to have a fatal reaction known as eczema vaccinatum (EV). Keyhole limpet hemocyanin (KLH) is a protein that can be used to deliver vaccines to the body. The purpose of this study is to determine a baseline immune reaction to KLH in people without AD. Once this has been established, other studies can be designed to determine whether KLH can be used to give vaccines to people with AD.

Interventions

  • BIOLOGICAL KLH carrier-protein

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2007-12
Est. Completion 2008-12
Phase Phase 1

What the finished NCT00614731 record still lists

NCT00614731 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 25 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (58% lower).

The record links to 0 conditions, and to 1 intervention - of which KLH carrier-protein is the first listed.

NCT00614731 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00614731 about?

NCT00614731 is a clinical study titled "Responses to Immunization With Keyhole Limpet Hemocyanin Administered by Scarification and the Intradermal Route". Atopic dermatitis (AD) is a skin disorder in which people often have swelling and skin infections. People with this disease cannot receive the smallpox vaccine because it could cause them to have a fatal reaction known as eczema vaccinatum (EV). Keyhole limpet hemocyanin (KLH) is a protein that can ...

What is the current status of trial NCT00614731?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 25 participants. The study started on 2007-12. Estimated completion is 2008-12.

What interventions are being tested in trial NCT00614731?

The interventions under investigation include: KLH carrier-protein (BIOLOGICAL).

Who is sponsoring clinical trial NCT00614731?

This trial is sponsored by National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00614731's enrollment target sits among peer trials

25 1495th of 2000 higher than 481 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other 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 NCT00614731, the US trial registry maintained by the National Library of Medicine. NCT00614731 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.