A study of sequential administration of oral sapacitabine and oral Seliciclib in patients with advanced solid tumors.
The primary objective of this study is to determine the maximum tolerated dose (MTD) or recommended phase II doses of sapacitabine and seliciclib administered sequentially or concomitantly. The secondary objectives are to evaluate antitumor activity of this sequential or concomitant treatment and to explore the pharmacodynamic effect of this treatment in skin and peripheral blood mononuclear cells.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
103
sequential or concomitant administration of sapacitabine and seliciclib
Dana Farber Cancer Institute
Boston, Massachusetts, United States
Dana Farber Cancer Institute
Boston, Massachusetts, United States
maximum tolerated dose
MTD of both sapacitabine and seliciclib administered sequentially in advanced solid tumor patients
Time frame: 1-3 months
tumor response rate
Anti-tumor activity of the sequential treatment of sapacitabine and seliciclib in patients with advanced solid tumors.
Time frame: 1-3 months
pharmacodynamic effects in skin and peripheral mononuclear cells
PD effect of the sequential treatment of sapacitabine and seliciclib in patients with advanced solid tumors.
Time frame: 1-3 months
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