drugset / Trial / NCT00722293

A Phase I, Open-label, Study of Pazopanib in Combination With Epirubicin or Doxorubicin for Advanced Solid Tumors

NCT00722293

Phase 1 Completed 111 enrolled GlaxoSmithKline
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This is an open-label, four-arm, Phase I, dose escalation study to evaluate the safety and tolerability and to determine the optimal tolerated regimen (OTR) of pazopanib in combination with epirubicin or doxorubicin in patients with advanced solid tumors. Patients will be enrolled in cohorts of 3 to receive escalating doses of pazopanib and epirubicin or doxorubicin. Dose escalation schemas for each study arm are described in the protocol. For each arm, the OTR will be defined as the highest dose combination of the agents where no more than one out of six patients experiences a dose-limiting toxicity. Twelve additional patients in each arm will be studied with the OTR to evaluate toxicity and pharmacokinetics. This will allow an assessment of potential drug-drug interactions. Antitumor activity will be assessed using RECIST criteria.

Timeline

Start
2008-07-08
Primary completion
2012-06-11
Completion
2014-02-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Doxorubicin Other / unclassified 60 mg/m2 Intravenous
Subject Doxorubicin Other / unclassified 75 mg/m2 Intravenous
Subject Epirubicin Small molecule 60 mg/m2 Intravenous
Subject Epirubicin Small molecule 90 mg/m2 Intravenous
Subject Pazopanib Small molecule 200 mg Oral
Subject Pazopanib Small molecule 400 mg Oral
Subject Pazopanib Small molecule 800 mg Oral

Indications