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Brief Title: Pharmacokinetics (PK) of TKI258 in Cancer Patients With Normal and Impaired Hepatic Function
Official Title: A Multi-center, Open Label Study to Assess Pharmacokinetics of TKI258 in Adult Cancer Patients With Normal and Impaired Hepatic Function
Study ID: NCT01443481
Brief Summary: This is a multi-center, open label study to assess pharmacokinetics (PK) of TKI258 at single-dose and steady state in adult cancer patients either with mild, moderate or severe hepatic impairment or with normal hepatic function. Hepatic function in study patients will be categorized as normal, mild, moderate or severe based upon pre-dose (Day 1) total bilirubin and AST/ALT levels. Starting dose of TKI258 will depend on total bilirubin and ALT/AST levels at baseline. Patients will be treated until disease progression (assessed by RECIST 1.1), unacceptable toxicity, death or discontinuation from the study treatment for any other reason.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
University of California at Los Angeles Dept. of UCLA (4), Los Angeles, California, United States
Duke University Medical Center DUMC, Durham, North Carolina, United States
Cancer Therapy & Research Center / UT Health Science Center SC, San Antonio, Texas, United States
Novartis Investigative Site, Gent, , Belgium
Novartis Investigative Site, Frankfurt, , Germany
Novartis Investigative Site, Hannover, , Germany
Novartis Investigative Site, Milano, MI, Italy
Novartis Investigative Site, Rozzano, MI, Italy
Novartis Investigative Site, Verona, VR, Italy
Novartis Investigative Site, Amsterdam, , Netherlands
Novartis Investigative Site, Maastricht, , Netherlands
Novartis Investigative Site, Singapore, , Singapore
Name: Novartis Pharmaceuticals
Affiliation: Novartis Pharmaceuticals
Role: STUDY_DIRECTOR