ACP-196 (Acalabrutinib) in Combination With Pembrolizumab, for Treatment of Hematologic Malignancies
NCT02362035
Blood Protein Disorders, Burkitt Lymphoma
Tucson, Arizona, United States
View Trial DetailsNCT Number: NCT01720758
The presence of a specific mutation in the gene known as B-RAF has been found in patients who have Hairy Cell Leukemia. In this study this specific mutation known as V600E will be ascertained in peripheral blood samples of patients who have this disease and in a group of patients who have a similar chronic lymphoproliferative conditions such as splenic marginal lymphoma. The finding of this specific mutation will help to verify or exclude the diagnosis of Hairy Cell Leukemia and determine whether patients are in remission.
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Notify Me18 year and older
All sexes
Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Patients over the age of 18 years -
Exclusion criteria
Patients less than 18 years in age or mentally defectives.
-
Time frame: 2 weeks
HaEmek Medical Center, Israel
Other
Assessment of the V600E Mutation in the B-RAF Gene in Chronic Lymphoproliferative Disease.
Acronym: B-RAF V600E
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