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NCT00776295 · ClinicalTrials.gov registry record · Phase 2

Autologous SCT Followed by Dendritic Cell p53 Vaccination in Patients With Limited Stage Small Cell Lung Cancer

A Phase 2 study, sponsored by H. Lee Moffitt Cancer Center and Research Institute.

Terminated
Registry status
Phase 2
Development phase
2
Enrollment target

NCT00776295: Clinical Trial Phase 2 study, sponsored by H. Lee Moffitt Cancer Center and Research Institute.

NCT00776295 is a Phase 2 study that was terminated before completion, run by H. Lee Moffitt Cancer Center and Research Institute. The registered enrollment target is 2 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00776295, a Phase 2 study, was terminated before completion, sponsored by H. Lee Moffitt Cancer Center and Research Institute.

TERMINATED
Registry status
Phase 2
Development phase
2 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether p53 vaccination followed by high dose chemotherapy and autologous HCT and T cell therapy significantly induces immune responses resulting in 1-year survival greater that the current 70%.

Primary Outcome

Number of participants with overall survival from first day of cyclophosphamide and GM-CSF mobilization to the day of death

Interventions

  • BIOLOGICAL Combined adenovirus vectored p53 tranfected dedritic cell vaccine and ex vivo expanded T-lymphocytes

Trial Details

FieldValue
Enrollment Target 2 participants
Start Date 2007-05
Est. Completion 2010-08
Phase Phase 2

Why NCT00776295 stopped before completion

NCT00776295 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 2 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which Combined adenovirus vectored p53 tranfected dedritic cell vaccine and ex vivo expanded T-lymphocytes is the first listed.

NCT00776295 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00776295 about?

NCT00776295 is a clinical study titled "Autologous SCT Followed by Dendritic Cell p53 Vaccination in Patients With Limited Stage Small Cell Lung Cancer". The purpose of this study is to determine whether p53 vaccination followed by high dose chemotherapy and autologous HCT and T cell therapy significantly induces immune responses resulting in 1-year survival greater that the current 70%.

What is the current status of trial NCT00776295?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 2 participants. The study started on 2007-05. Estimated completion is 2010-08.

What interventions are being tested in trial NCT00776295?

The interventions under investigation include: Combined adenovirus vectored p53 tranfected dedritic cell vaccine and ex vivo expanded T-lymphocytes (BIOLOGICAL).

Who is sponsoring clinical trial NCT00776295?

This trial is sponsored by H. Lee Moffitt Cancer Center and Research Institute, which has 502 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00776295's enrollment target sits among peer trials

2 2001st of 2000 the lowest 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 NCT00776295, the US trial registry maintained by the National Library of Medicine. NCT00776295 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.