This phase I trial studies the side effects and the best dose of pazopanib hydrochloride in treating patients with solid tumors that has spread to other places in the body and usually cannot be cured or controlled with treatment (advanced) or does not respond to treatment (refractory). Pazopanib hydrochloride may prevent the growth of new blood vessels that tumors need to grow. Studying samples of blood in the laboratory from patients receiving pazopanib hydrochloride may help doctors learn more about the effects of the body on the drug. It may also help doctors understand how well patients respond to treatment.
Age range
18 Years
Sex
ALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Biologically optimal dose (BOD) defined as the dose level and diet in combination that induces no toxicity requiring dose modification per protocol and achieves a satisfactory pazopanib trough concentration (Cmin greater than 30 ug/mL)
Timeframe: At 14 days
Adverse events profile, as assessed by the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 4.0
Timeframe: Up to 3 months
Incidence of grade 3+ adverse events, as assessed by the NCI CTCAE version 4.0
Timeframe: Up to 3 months
Toxicity profile, as assessed by the NCI CTCAE version 4.0
Timeframe: Up to 3 months
Response profile, assessed using modified Response Evaluation Criteria in Solid Tumors (RECIST)
Timeframe: Up to 3 months
Time until any treatment-related toxicity, as assessed by the NCI CTCAE version 4.0
Timeframe: Up to 3 months
Time until treatment-related grade 3+ toxicity, as assessed by the NCI CTCAE version 4.0
Timeframe: Up to 3 months
Time until hematologic nadirs (ANC, platelets, hemoglobin) , as assessed by the NCI CTCAE version 4.0
Timeframe: Up to 3 months
Time to progression according to RECIST version 1.1
Timeframe: Up to 3 months
Time to treatment failure
Timeframe: From registration to documentation of progression, unacceptable toxicity, or refusal to continue participation by the patient, assessed up to 3 months