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NCT00450008 · ClinicalTrials.gov registry record · Phase 2
Safety and Efficacy Study of GM-CSF, Thalidomide Plus Docetaxel in Prostate Cancer
A Phase 2 study, sponsored by The Methodist Hospital Research Institute.
- Terminated
- Registry status
- Phase 2
- Development phase
- 9
- Enrollment target
NCT00450008 is a Phase 2 study that was terminated before completion, run by The Methodist Hospital Research Institute. The registered enrollment target is 9 participants.
The verdict
NCT00450008, a Phase 2 study, was terminated before completion, sponsored by The Methodist Hospital Research Institute.
- TERMINATED
- Registry status
- Phase 2
- Development phase
- 9 participants
- Enrollment target
Study Summary
The purpose of this study is to assess the relative efficacy and toxicity of combination therapy of GM-CSF, Thalidomide plus Docetaxel in patients with prostate cancer with a rising PSA.
Interventions
- DRUG docetaxel
- DRUG GM-CSF
- DRUG thalidomide
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 9 participants |
| Start Date | 2006-12 |
| Est. Completion | 2008-09 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00450008
The ClinicalTrials.gov registry entry for NCT00450008 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 9 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The Methodist Hospital Research Institute, which has 126 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which docetaxel is the first listed.
NCT00450008 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00450008 about?
NCT00450008 is a clinical study titled "Safety and Efficacy Study of GM-CSF, Thalidomide Plus Docetaxel in Prostate Cancer". The purpose of this study is to assess the relative efficacy and toxicity of combination therapy of GM-CSF, Thalidomide plus Docetaxel in patients with prostate cancer with a rising PSA.
What is the current status of trial NCT00450008?
This trial is currently terminated. It is a Phase 2 study. The enrollment target is 9 participants. The study started on 2006-12. Estimated completion is 2008-09.
What interventions are being tested in trial NCT00450008?
The interventions under investigation include: docetaxel (DRUG), GM-CSF (DRUG), thalidomide (DRUG).
Who is sponsoring clinical trial NCT00450008?
This trial is sponsored by The Methodist Hospital Research Institute, which has 126 total clinical trials registered on ClinicalTrials.gov.
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