Myelofibrosis Clinical Trial
Official title:
Polycythemia Vera, Myelofibrosis and Essential Thrombocythemia: Identification of PV, MF & ET Genes
The purpose of this project is to find genes whose mutations cause Polycythemia Vera, Essential Thrombocythemia and Primary Myelofibrosis.
Polycythemia Vera (PV), Essential Thrombocythemia (ET) and Primary Myelofibrosis (PMF), also
known as the Philadelphia Chromosome negative myeloproliferative disorders (MPDs), are not
congenital, but acquired. The purpose of this project is to find genes whose mutations cause
these disorders, as well as improve diagnostic measures for these diseases. When this is
accomplished new therapies to control and eventually cure the disease can be designed.
All subjects will be asked to donate 4-6 teaspoons of blood. On occasion, if the blood cells
from a particular sample do not grow well and the DNA from that sample is used up or other
tests are needed, we may ask to collect additional samples. In patients who have undergone a
bone marrow biopsy as part of their clinical evaluation, we will test the reproducibility
between pathologists for the revised 2008 WHO diagnostic criteria to diagnose
myeloproliferative disorders (MPD).
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| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
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||
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Phase 1 | |
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Phase 2 | |
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||
| Completed |
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Phase 2 | |
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Phase 1/Phase 2 | |
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Phase 1 | |
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|
Phase 3 | |
| Not yet recruiting |
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Phase 1 |