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NCT00431054 · ClinicalTrials.gov registry record · Phase 1
Perifosine and Docetaxel in Patients With Relapsed Epithelial Ovarian Cancer
A Phase 1 study, sponsored by M.D. Anderson Cancer Center.
- Completed
- Registry status
- Phase 1
- Development phase
- 22
- Enrollment target
NCT00431054: Completed Phase 1 study, sponsored by M.D. Anderson Cancer Center.
NCT00431054 is a Phase 1 study that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 22 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (63% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00431054, a Phase 1 study, has completed, sponsored by M.D. Anderson Cancer Center.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 22 participants
- Enrollment target
Study Summary
The goal of this clinical research study is to find out if a combination treatment of perifosine and docetaxel will help shrink or slow the growth of cancer cells in recurrent ovarian cancer. The safety of this combination treatment will also be studied.
Interventions
- DRUG Docetaxel
- DRUG Perifosine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 22 participants |
| Start Date | 2007-02 |
| Est. Completion | 2012-05 |
| Phase | Phase 1 |
What the finished NCT00431054 record still lists
NCT00431054 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 22 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (63% lower).
The record links to 0 conditions, and to 2 interventions - of which Docetaxel is the first listed.
NCT00431054 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00431054 about?
NCT00431054 is a clinical study titled "Perifosine and Docetaxel in Patients With Relapsed Epithelial Ovarian Cancer". The goal of this clinical research study is to find out if a combination treatment of perifosine and docetaxel will help shrink or slow the growth of cancer cells in recurrent ovarian cancer. The safety of this combination treatment will also be studied.
What is the current status of trial NCT00431054?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 22 participants. The study started on 2007-02. Estimated completion is 2012-05.
What interventions are being tested in trial NCT00431054?
The interventions under investigation include: Docetaxel (DRUG), Perifosine (DRUG).
Who is sponsoring clinical trial NCT00431054?
This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00431054's enrollment target sits among peer trials
22 1601st of 2000 higher than 386 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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