The aim of this study is to investigate the safety and tolerability of trichostatin A in individuals with relapsed or refractory hematologic malignancies.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
42
Intravenous Infusion
Vanda Investigational Site
Washington D.C., District of Columbia, United States
WITHDRAWNVanda Investigational Site
Lafayette, Indiana, United States
COMPLETEDVanda Investigational Site
Safety and tolerability of trichostatin A measured by spontaneous reporting of adverse events (AEs)
Measured by spontaneous reporting of adverse events (AEs)
Time frame: Up to 24 months
Dose-limiting toxicities (DLTs) and maximum tolerated dose (MTD) of trichostatin A
Time frame: Up to 24 months
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Hackensack, New Jersey, United States
Vanda Investigational Site
Seattle, Washington, United States
COMPLETEDVanda Investigational Site
Biała Podlaska, Poland
RECRUITINGVanda Investigational Site
Katowice, Poland
RECRUITINGVanda Investigational Site
Krakow, Poland
COMPLETEDVanda Investigational Site
Opole, Poland
RECRUITINGVanda Investigational Site
Skorzewo, Poland
COMPLETEDVanda Investigational Site
Warsaw, Poland
RECRUITING...and 1 more locations