This study is being conducted to assess the safety, tolerability and PK of AZD1480 in patients with advanced solid malignancies.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
72
continuous daily oral capsule
Research Site
Aurora, Colorado, United States
Research Site
Detroit, Michigan, United States
Research Site
Philadelphia, Pennsylvania, United States
Safety and tolerability as assessed by Adverse events, vital signs, ECGs, Pulmonary Function Tests (DLco, FEV, FVC, Oxygen saturation) and laboratory data (chemistry, hematology and Urinalysis)
Time frame: Information will be collected from the time the informed consent is signed, throughout the study
Evaluation of the pharmacokinetics of AZD1480
Time frame: During all cycles
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