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NCT00938223 · ClinicalTrials.gov registry record · Phase 2

Evaluation of the Immunogenicity of Vaccination With Multiple Synthetic Melanoma Peptides With Granulocyte-macrophage Colony-stimulating Factor (GM-CSF)-In-Adjuvant, in Patients With Advanced Melanoma

A Phase 2 study, sponsored by Craig L Slingluff, Jr.

Completed
Registry status
Phase 2
Development phase
51
Enrollment target

NCT00938223: Completed Phase 2 study, sponsored by Craig L Slingluff, Jr.

NCT00938223 is a Phase 2 study that has completed, run by Craig L Slingluff, Jr. The registered enrollment target is 51 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (62% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00938223, a Phase 2 study, has completed, sponsored by Craig L Slingluff, Jr.

COMPLETED
Registry status
Phase 2
Development phase
51 participants
Enrollment target

Study Summary

This is an open-label, phase II study of a vaccine comprising melanoma peptides and a tetanus helper peptide, administered in GM-CSF-in-adjuvant. Patients will be randomized to receive one of two different vaccine regimens. Patients will be stratified by stage of disease (IIB versus III versus IV).

Interventions

  • BIOLOGICAL 4-peptide and 12-peptide melanoma vaccines

Trial Details

FieldValue
Enrollment Target 51 participants
Start Date 2000-08
Phase Phase 2
Craig L Slingluff, Jr

23 total trials

What the finished NCT00938223 record still lists

NCT00938223 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 51 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (62% lower).

The record links to 0 conditions, and to 1 intervention - of which 4-peptide and 12-peptide melanoma vaccines is the first listed.

NCT00938223 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00938223 about?

NCT00938223 is a clinical study titled "Evaluation of the Immunogenicity of Vaccination With Multiple Synthetic Melanoma Peptides With Granulocyte-macrophage Colony-stimulating Factor (GM-CSF)-In-Adjuvant, in Patients With Advanced Melanoma". This is an open-label, phase II study of a vaccine comprising melanoma peptides and a tetanus helper peptide, administered in GM-CSF-in-adjuvant. Patients will be randomized to receive one of two different vaccine regimens. Patients will be stratified by stage of disease (IIB versus III versus IV).

What is the current status of trial NCT00938223?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 51 participants. The study started on 2000-08.

What interventions are being tested in trial NCT00938223?

The interventions under investigation include: 4-peptide and 12-peptide melanoma vaccines (BIOLOGICAL).

Who is sponsoring clinical trial NCT00938223?

This trial is sponsored by Craig L Slingluff, Jr, which has 23 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00938223's enrollment target sits among peer trials

51 1190th of 2000 higher than 806 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT00938223, the US trial registry maintained by the National Library of Medicine. NCT00938223 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.