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NCT00267085 · ClinicalTrials.gov registry record · Phase 2
Synthetic Vaccine in Patients With Chronic Myeloid Leukemia and Minimal Residual Disease
A Phase 2 study of Chronic Myeloid Leukemia and Minimal Residual Disease, sponsored by M.D. Anderson Cancer Center.
- Completed
- Registry status
- Phase 2
- Development phase
- 11
- Enrollment target
- 1
- Study location
NCT00267085 is a Phase 2 study of Chronic Myeloid Leukemia and Minimal Residual Disease that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 11 participants, below the 210-participant average among 35 other Chronic Myeloid Leukemia trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00267085, a Phase 2 study of Chronic Myeloid Leukemia and Minimal Residual Disease, has completed, sponsored by M.D. Anderson Cancer Center.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 11 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this clinical research study is to learn if giving 1 of 2 CML (Chronic Myeloid Leukemia) vaccines (CML-VAX B2 or CML-VAX B3) together with imatinib mesylate can decrease or eliminate all evidence of disease in patients who have CML that is in remission after treatment with imatinib mesylate, but who still have small amounts of detectable disease.
Conditions Studied
Interventions
- BIOLOGICAL Synthetic Tumor-Specific Breakpoint Peptide Vaccine
Study Locations (1)
Texas
- UT MD Anderson Cancer Center - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 11 participants |
| Start Date | 2005-12 |
| Est. Completion | 2008-07 |
| Phase | Phase 2 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00267085
The ClinicalTrials.gov registry entry for NCT00267085 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 11 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 210-participant average among 35 other Chronic Myeloid Leukemia trials with a reported enrollment target (95% lower). The listed sponsor is M.D. Anderson Cancer Center, which has 2,692 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Chronic Myeloid Leukemia appearing as the primary indexed condition, and to 1 intervention - of which Synthetic Tumor-Specific Breakpoint Peptide Vaccine is the first listed.
NCT00267085 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT00267085 about?
NCT00267085 is a clinical study titled "Synthetic Vaccine in Patients With Chronic Myeloid Leukemia and Minimal Residual Disease". The goal of this clinical research study is to learn if giving 1 of 2 CML (Chronic Myeloid Leukemia) vaccines (CML-VAX B2 or CML-VAX B3) together with imatinib mesylate can decrease or eliminate all evidence of disease in patients who have CML that is in remission after treatment with imatinib mesyl...
What is the current status of trial NCT00267085?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 11 participants. The study started on 2005-12. Estimated completion is 2008-07.
What conditions does trial NCT00267085 study?
This clinical trial studies the following conditions: Chronic Myeloid Leukemia, Minimal Residual Disease.
What interventions are being tested in trial NCT00267085?
The interventions under investigation include: Synthetic Tumor-Specific Breakpoint Peptide Vaccine (BIOLOGICAL).
Who is sponsoring clinical trial NCT00267085?
This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00267085 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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