Status:
COMPLETED
A Two-way Crossover Study Of The Effect Of Food On The Pharmacokinetics Of Pazopanib In Cancer Patients
Lead Sponsor:
GlaxoSmithKline
Conditions:
Carcinoma, Renal Cell
Eligibility:
All Genders
21+ years
Phase:
PHASE1
Brief Summary
This is two-part study (Part I/Part II). Part I is designed to determine the effect of a low and high fat meal on the pharmacokinetics of single dose pazopanib (GW572016). Part II is designed to allow...
Eligibility Criteria
Inclusion
- Inclusion criteria:
- Histologically or cytologically confirmed diagnosis of advanced solid tumors that have progressed following treatment with standard agents. Patients may have either measurable disease by RECIST or may be followed by a tumor marker for assessment of disease.
- Eastern Cooperative Oncology Group performance status of 0 or 1.
- Adequate bone marrow function: ANC greater than or equal to 1,500 mm cubed; Platelets count greater than or equal to 100,000 mm cubed; Hgb greater than or equal to 9 g per dL
- Adequate renal function as determined by a creatinine clearance greater than 50mL per min calculated by the Cockcroft-Gault Formula; Measured creatinine clearance greater than or equal to 50mL per min by 24-hour urine collection will be acceptable in lieu of a calculated value.
- Urine Creatinine Ratio of less than 1 as assessed in a random or spot urine sample.
- Adequate hepatic function: total bilirubin less than or equal to 1.5 times the upper limit of normal; AST and ALT less than or equal to 2.5 times the upper limit of normal.
- PT, INR, PTT less than or equal to 1.2 times upper limit of normal.
- Male or female at least 18 years of age.
- A woman is eligible to enter and participate in the study if she is of: Non-childbearing potential; Childbearing potential, has a negative serum pregnancy test at screening, and agrees to use adequate contraception per protocol. A man with a female partner of childbearing potential is eligible to enter and participate in the study if he uses a barrier method of contraception or abstinence during the study. If sexually active, patients will continue the recommended contraceptive measures for the duration of the treatment and for 28 days following discontinuation of therapy.
- Predicted life expectancy of at least 12 weeks.
- Written informed consent.
- Able to swallow and retain oral medications.
- Exclusion criteria:
- Patients with certain heart problems or history of bleeding within a month.
Exclusion
Key Trial Info
Start Date :
September 21 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 19 2009
Estimated Enrollment :
28 Patients enrolled
Trial Details
Trial ID
NCT00363194
Start Date
September 21 2006
End Date
June 19 2009
Last Update
November 17 2017
Active Locations (2)
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1
GSK Investigational Site
Indianapolis, Indiana, United States, 46202
2
GSK Investigational Site
Detroit, Michigan, United States, 48201