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Clinical Trial Summary

This is a Phase 1 study during which patients with low or intermediate-1 risk myelodysplastic syndromes (MDS) will receive investigational study drug ARRY-614.

This study has 2 parts. In the first part, patients will receive increasing doses of study drug in order to achieve the highest dose of the study drug possible that will not cause unacceptable side effects. Approximately 50 patients from the US will be enrolled in Part 1 (Completed).

In the second part of the study, patients will receive the best dose of study drug determined from the first part of the study and will be followed to see what side effects and effectiveness the study drug has, if any, in treating the cancer. Approximately 30 patients from the US will be enrolled in Part 2 (Completed).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01496495
Study type Interventional
Source Array BioPharma
Contact
Status Completed
Phase Phase 1
Start date January 2012
Completion date March 18, 2015

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