Phase I Mass Balance, PK and Safety Study of 14C-Labeled Belinostat in Patients With Advanced Cancer

1. Signed informed consent document indicating understanding of the purpose of and procedures required for the study and willingness to participate in the study.
2. Histological confirmation of cancer and refractory or intolerant to standard therapy or cancer for which no standard therapy exists.
3. Age at study entry of 18 years or older.
4. Availability to stay in the research unit for the first 7 days.
5. Adequate renal function defined as a calculated creatinine clearance (CrCl) of > 45 mL/minute.
6. Adequate hepatic function: total bilirubin \< 1.5 x the upper limits of normal (ULN), aspartate aminotransferase (AST) and alanine aminotransferase (ALT) \< 2.5 x ULN.
7. Adequate hematopoietic function defined as an absolute neutrophil count (ANC) > 1000 cells/µL and platelet count > 50,000/µL.
8. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
9. Life expectancy of at least 12 weeks.
10. If female, patient must be postmenopausal for at least 1 year, documented surgically sterile (bilateral tubal ligation, bilateral oophorectomy or hysterectomy), or of childbearing potential and practicing birth control. Acceptable contraceptive methods in this study are intrauterine device; diaphragm or condom in combination with spermicidal foam or jelly; injectable, implantable, or transdermal patch; or oral contraception.
11. Female patients must have a negative pregnancy test at the Screening Visit and at the end of study treatment (30 days after the last dose of belinostat).

Exclusion Criteria:

1. Known anal or urinary incontinence.
2. Diagnosis of acute myelogenous leukemia (AML), multiple myeloma, primary hepatic or renal carcinomas.
3. Inability to consume oral fluids.
4. Treatment with drugs known to inhibit metabolic pathways (glucuronidation, CYP system) in the 4 weeks before the Screening Visit.
5. Concurrent treatment with diuretics or laxatives.
6. Radiotherapy involving mouth, esophagus, and gastrointestinal tract in the 4 weeks before the Screening Visit.
7. Polymorphism in UGT1A1.
8. Known diagnosis of human immunodeficiency virus (HIV), hepatitis B or C.
9. Previous participation in a study utilizing 14C.
10. Body surface area \< 1.5 m2.
11. Ongoing or medical history of a physical or psychiatric illness, significant comorbidity, or any medical disorder other than cancer that may require treatment or make the subject unlikely to fully complete the study.
12. Use of another investigational product or anticancer agent within 4 weeks prior to the Screening Visit.