drugset / Trial / NCT01165385

Study With Pazopanib in Combination With Cisplatin (CDDP) in Patients With Advanced Solid Tumors

NCT01165385

Phase 1 Completed 35 enrolled UNICANCER
NaSingle-groupOpen-labelTreatment

Summary

The aim of this research is to evaluate the potential interest of an association of Pazopanib, a multi-tyrosine kinase inhibitor, and cisplatin. As cisplatin has marketing approval for several cancers (ovarian, testicle, bladder, esophagus, endometrium, lung, stomach, head and neck cancer (HNC)), and in order to have a rapid evaluation of this combination, we will evaluate the combination in any patient whose tumors is known to be sensible to cisplatin (except tumors at risk of bleeding). This study is a classical phase 1 trial of pazopanib and 3-weekly cisplatin association. It will allow for optimal dose selection and pharmacokinetic analysis. It is planed to include around 38 patients, enriching the optimal tolerated regimen (OTR) level only with a cohort of triple negative breast cancer patients. If the association is proven to be feasible, we will then move to a specific phase II study in triple negative breast cancer patients.

Timeline

Start
2010-06
Primary completion
2013-10
Completion
2014-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Cisplatin Other / unclassified 60 mg/m2 Intravenous
Subject Cisplatin Other / unclassified 75 mg/m2 Intravenous
Subject Cisplatin Other / unclassified 100 mg/m2 Intravenous
Subject Pazopanib Small molecule 400 mg Oral
Subject Pazopanib Small molecule 600 mg Oral
Subject Pazopanib Small molecule 800 mg Oral