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NCT00327288 · ClinicalTrials.gov registry record · Phase 1

Safety Study of Imexon Plus Docetaxel in Lung, Breast or Prostate Cancer Patients

A Phase 1 study, sponsored by AmpliMed Corporation.

Completed
Registry status
Phase 1
Development phase
34
Enrollment target

NCT00327288: Completed Phase 1 study, sponsored by AmpliMed Corporation.

NCT00327288 is a Phase 1 study that has completed, run by AmpliMed Corporation. The registered enrollment target is 34 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (43% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00327288, a Phase 1 study, has completed, sponsored by AmpliMed Corporation.

COMPLETED
Registry status
Phase 1
Development phase
34 participants
Enrollment target

Study Summary

Protocol AMP-010 is a Phase 1b study of imexon plus docetaxel for patients with previously treated breast cancer, previously treated lung cancer or hormone refractory prostate cancer. Docetaxel is approved by the Food and Drug Administration (FDA) as a second line therapy for these cancers. The imexon is administered on days 1-5 and the docetaxel on day 1 of every 3 week cycle. The objective of the protocol is to determine the highest dose of imexon which can be given with a full dose of docetaxel, and to provide information to enable the design of a future study focused on one or more specific cancer types.

Interventions

  • DRUG docetaxel
  • DRUG imexon

Trial Details

FieldValue
Enrollment Target 34 participants
Start Date 2005-10
Est. Completion 2008-07
Phase Phase 1
AmpliMed Corporation

6 total trials

What the finished NCT00327288 record still lists

NCT00327288 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 34 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (43% lower).

The record links to 0 conditions, and to 2 interventions - of which docetaxel is the first listed.

NCT00327288 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00327288 about?

NCT00327288 is a clinical study titled "Safety Study of Imexon Plus Docetaxel in Lung, Breast or Prostate Cancer Patients". Protocol AMP-010 is a Phase 1b study of imexon plus docetaxel for patients with previously treated breast cancer, previously treated lung cancer or hormone refractory prostate cancer. Docetaxel is approved by the Food and Drug Administration (FDA) as a second line therapy for these cancers. The imex...

What is the current status of trial NCT00327288?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 34 participants. The study started on 2005-10. Estimated completion is 2008-07.

What interventions are being tested in trial NCT00327288?

The interventions under investigation include: docetaxel (DRUG), imexon (DRUG).

Who is sponsoring clinical trial NCT00327288?

This trial is sponsored by AmpliMed Corporation, which has 6 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00327288's enrollment target sits among peer trials

34 1273rd of 2000 higher than 721 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 NCT00327288, the US trial registry maintained by the National Library of Medicine. NCT00327288 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.