A Study of the Efficacy of MK-0683 in Patients With Polycythaemia Vera and Essential Thrombocythaemia
This trial is active, not recruiting.
|Conditions||polycythemia vera, essential thrombocythemia|
|Treatment||hdac inhibitor (mk-0683)|
|Sponsor||Copenhagen University Hospital at Herlev|
|Start date||February 2009|
|End date||August 2012|
|Trial size||60 participants|
|Trial identifier||NCT00866762, MK-0683/092-0|
The aim of the present study is to evaluate the efficacy and safety of MK-0683 in the treatment of PV and ET. This agent has most recently been shown to be a potent inhibitor of the autonomous proliferation of haematopoietic cells of PV and ET patients carrying the JAK2 V617F mutation. Accordingly, it may be anticipated that MK-0683 - by decreasing the JAK2 allele burden - may influence clonal myeloproliferation and in vivo granulocyte, platelet and endothelial activation , which are considered to be major determinants of morbidity and mortality ( thrombosis, bleeding, extramedullary haematopoiesis , myelofibrosis ) in these disorders. The effects of MK-0683 at the molecular level will be studied by global/ focused gene expression profiling, epigenome profiling and proteomics.
|United States||No locations recruiting|
|Other countries||No locations recruiting|
|Copenhagen, Denmark||Copenhagen University Hospital Rigshospitalet||no longer recruiting|
|Esbjerg, Denmark||Esberg Hospital||no longer recruiting|
|Herlev, Denmark||Herlev Hospital||no longer recruiting|
|Odense, Denmark||Odense University Hospital||no longer recruiting|
|Roskilde, Denmark||Roskilde Hospital||no longer recruiting|
|Viborg, Denmark||Regional Hospital Viborg||no longer recruiting|
|Amsterdam, Netherlands||VU University Medical Centre||no longer recruiting|
|Orebro, Sweden||University Hospital Orebro||no longer recruiting|
|Stockholm, Sweden||Stockholm South General Hospital (Sodersjukhuset)||no longer recruiting|
|Stockholm, Sweden||Karolinska University Hospital Huddinge||no longer recruiting|
|Uddevalla, Sweden||Sahlgrenska University Hospital & Uddevalla Hospital||no longer recruiting|
|Uppsala, Sweden||Uppsala University Hospital||no longer recruiting|
|Belfast, United Kingdom||Centre for Cancer Research and Cell Biology, Queen's University Belfast||no longer recruiting|
|Cardiff, United Kingdom||Cardiff University||no longer recruiting|
|Dudley, United Kingdom||Russell's Hall Hospital||no longer recruiting|
|London, United Kingdom||St Thomas' Hospital||no longer recruiting|
|Endpoint classification||efficacy study|
|Intervention model||single group assignment|
Treatment with study drug approximately 6 months and follow-up for 3 months
To evaluate the efficacy of study drug (MK-0683) in the treatment of patients with PV and ET.
time frame: one year
To study changes in bone marrow morphology before and after treatment with study drug.
time frame: one year
Male or female participants at least 18 years old.
Inclusion Criteria: - Male or female patient > 18 years of age AND - A confirmed diagnosis of PV AND - Biochemical evidence of active disease as defined by: - a need for phlebotomy within last 3 months - a leukocyte count > 10 x 10^9/L in the absence of infection or inflammation (normal CRP) and/or (PV/ET) - a platelet count > 450 x 10^9/L in the absence of infection or inflammation (normal CRP)(PV/ET) OR - Male or female patient > 18 years of age AND - A confirmed diagnosis of ET AND - Biochemical evidence of active disease as defined by *a platelet count > 450 x 10^9/L in the absence of infection or inflammation Inclusion Criteria for both PV and ET: - Newly diagnosed or previously treated patient in chronic phase OR - Advanced phase PV or ET as defined by blasts of > 1 x 10^9/L in the peripheral blood and/or white cell count > 30 x 10^9/L OR - Resistant or refractory PV or ET as defined by haemoglobin < 10.5 gm/dl with a platelet count > 600 x 10^9/L on current therapy OR - Cycling platelet counts on therapy OR - Intolerant to other therapies defined by patients with PV or ET who have side effects on current therapies preventing continuation (leg ulcers on hydroxycarbamide, unacceptable fatigue etc on interferon) Exclusion Criteria: - A platelet count > 1500 x 10^9/L (a need for cytoreduction in platelet count) - Patients of childbearing potential without a negative pregnancy test prior to initiation of study drug - Women who are breast feeding - Males and females not using contraceptives if sexually active. - EGOC Performance status Score > or = 3 - Serum creatinine more than 2 x's teh ULN - Total serum bilirubin more than 1.5 x's the ULN - Serum AST/ALT more than 3 x's the ULN - Interferon alpha within 1 week of day 1 - Hydroxycarbamide within 1 week of day 1 - Anagrelide within 1 week of day 1 - Valproic acid (as an anticonvulsant) within 28 days of day 1 - Any other investigational drug within 28 days of day 1 - Active HIV, HBV or HCV infection - Any serious concomitant disease or circumstances that could limit compliance with the study, including but not limited to the following: CTCAE grade 3-4 cardiac general & arrhythmia, or psychiatric or social conditions that may interfere with patient compliance. - Any prior malignancy with the exception of cervical intraepithelial neoplasia, basal cell carcinoma of the skin, or other localized malignancy that has undergone potentially curative therapy with no evidence of that disease for five years, and who is deemed to be at low risk for recurrence by his/her treating physician. - Patient has a known allergy or hypersensitivity to study drug.
|Official title||A Phase II Study of MK-0683 in Patients With Polycythaemia Vera and Essential Thrombocythaemia.|
|Principal investigator||Hans C Hasselbalch, MD|
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