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NCT00025233 · ClinicalTrials.gov registry record · Phase 2
Bevacizumab in Treating Patients With Persistent or Recurrent Cancer of the Cervix
A Phase 2 study of Cervical Squamous Cell Carcinoma and Recurrent Cervical Cancer, sponsored by National Cancer Institute (NCI).
- Completed
- Registry status
- Phase 2
- Development phase
- 50
- Enrollment target
- 1
- Study location
NCT00025233 is a Phase 2 study of Cervical Squamous Cell Carcinoma and Recurrent Cervical Cancer that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 50 participants, below the 119-participant average among 13 other Cervical Squamous Cell Carcinoma trials with a reported enrollment target (58% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00025233, a Phase 2 study of Cervical Squamous Cell Carcinoma and Recurrent Cervical Cancer, has completed, sponsored by National Cancer Institute (NCI).
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
This phase II trial is to see if bevacizumab works in treating patients who have persistent or recurrent cancer of the cervix. Monoclonal antibodies, such as bevacizumab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or deliver cancer-killing substances to them.
Conditions Studied
Interventions
- OTHER laboratory biomarker analysis
- BIOLOGICAL bevacizumab
Study Locations (1)
Pennsylvania
- Gynecologic Oncology Group - Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2002-04 |
| Est. Completion | 2009-07 |
| Phase | Phase 2 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00025233
The ClinicalTrials.gov registry entry for NCT00025233 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 119-participant average among 13 other Cervical Squamous Cell Carcinoma trials with a reported enrollment target (58% lower). The listed sponsor is National Cancer Institute (NCI), which has 3,257 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Cervical Squamous Cell Carcinoma appearing as the primary indexed condition, and to 2 interventions - of which laboratory biomarker analysis is the first listed.
NCT00025233 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT00025233 about?
NCT00025233 is a clinical study titled "Bevacizumab in Treating Patients With Persistent or Recurrent Cancer of the Cervix". This phase II trial is to see if bevacizumab works in treating patients who have persistent or recurrent cancer of the cervix. Monoclonal antibodies, such as bevacizumab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells an...
What is the current status of trial NCT00025233?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 50 participants. The study started on 2002-04. Estimated completion is 2009-07.
What conditions does trial NCT00025233 study?
This clinical trial studies the following conditions: Cervical Squamous Cell Carcinoma, Recurrent Cervical Cancer.
What interventions are being tested in trial NCT00025233?
The interventions under investigation include: laboratory biomarker analysis (OTHER), bevacizumab (BIOLOGICAL).
Who is sponsoring clinical trial NCT00025233?
This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00025233 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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