This study is a Phase I, open label study to determine the Maximum Tolerated Dose(MTD) and the Recommended Phase II Dose (RP2D) in patients with advanced solid tumors.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
28
Dosing will be orally, once a day for the duration of the trial.
University Hospital Basel
Basel, Switzerland
Maximum Tolerated Dose (MTD) and the Recommended Phase II Dose (RP2D)
Time frame: In average 1 year
To determine overall safety
Incidence of SAEs, incidence and severity of all AEs, changes of vital signs, physical examinations, body weight, changes of routine laboratory assessments.
Time frame: 1 year
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