In Vitro Evaluation of Immune Responses in Cutaneous T-Cell Lymphoma (CTCL)
Completed
Conditions studied: Cutaneous T-cell Lymphoma, Sezary Syndrome, Mycosis Fungoides
In brief
This is an in vitro evaluation of cutaneous T-cell lymphoma using patients' blood and tissue to evaluate immune responses related to identified tumor populations and dendritic/CD 8 cells.
Key facts
- Study ID
- NCT00177190
- Run by
- University of Pittsburgh
- People needed
- 8
- Starts
- 2002-06-01
- Expected to finish
- 2006-01-01
- Last updated by the study team
- 2014-05-28
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Males or females <18 years of age
- Histologically confirmed stage IV cutaneous T-cell lymphoma, with at least 5% of the peripheral blood lymphocytes showing atypical morphology consistent with Sezary cells
- Ambulatory and be in stable medical condition
- Biopsy positive mycosis fungoides/CTCL or clonal type of CTCL as determined by PCR for TCR and Southern blot for TCR
You may not qualify if…
- Received any chemotherapy or radiotherapy within 4 weeks prior to enrollment
- Significant psychiatric illness which would prevent adequate informed consent in the opinion of the principal investigator
- Systemic steroid therapy other than maintenance for adrenal suppression
- Known coagulopathy for non SS subjects.
Where it is running
- University of Pittsburgh Medical Center — Pittsburgh, Pennsylvania, United States
Full record on ClinicalTrials.gov
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