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NCT00121173 · ClinicalTrials.gov registry record · Phase 1

Vaccine Therapy in Preventing Cervical Cancer in Patients With Cervical Intraepithelial Neoplasia

A Phase 1 study, sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins.

Completed
Registry status
Phase 1
Development phase
16
Enrollment target

NCT00121173: Completed Phase 1 study, sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins.

NCT00121173 is a Phase 1 study that has completed, run by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins. The registered enrollment target is 16 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (73% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00121173, a Phase 1 study, has completed, sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins.

COMPLETED
Registry status
Phase 1
Development phase
16 participants
Enrollment target

Study Summary

RATIONALE: Vaccines made from protein and DNA may help the body build an effective immune response to kill abnormal cells in the cervix. The use of vaccine therapy may prevent cervical cancer. PURPOSE: This phase I/II trial is studying the side effects and best dose of vaccine therapy and to see how well it works in preventing cervical cancer in patients with cervical intraepithelial neoplasia and human papillomavirus.

Primary Outcome

Number of participants with serious adverse events (SAE) according to CTCAE 3.0 grading.

Interventions

  • BIOLOGICAL pNGVL4a-Sig/E7(detox)/HSP70 DNA vaccine

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2003-11
Est. Completion 2010-01
Phase Phase 1

What the finished NCT00121173 record still lists

NCT00121173 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 16 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (73% lower).

The record links to 0 conditions, and to 1 intervention - of which pNGVL4a-Sig/E7(detox)/HSP70 DNA vaccine is the first listed.

NCT00121173 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00121173 about?

NCT00121173 is a clinical study titled "Vaccine Therapy in Preventing Cervical Cancer in Patients With Cervical Intraepithelial Neoplasia". RATIONALE: Vaccines made from protein and DNA may help the body build an effective immune response to kill abnormal cells in the cervix. The use of vaccine therapy may prevent cervical cancer. PURPOSE: This phase I/II trial is studying the side effects and best dose of vaccine therapy and to see ho...

What is the current status of trial NCT00121173?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 16 participants. The study started on 2003-11. Estimated completion is 2010-01.

What interventions are being tested in trial NCT00121173?

The interventions under investigation include: pNGVL4a-Sig/E7(detox)/HSP70 DNA vaccine (BIOLOGICAL).

Who is sponsoring clinical trial NCT00121173?

This trial is sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, which has 523 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00121173's enrollment target sits among peer trials

16 1786th of 2000 higher than 203 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 NCT00121173, the US trial registry maintained by the National Library of Medicine. NCT00121173 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.