drugset / Trial / NCT00996346

Phase I/II Study of Irinotecan and Temsirolimus in Patients With Refractory Sarcomas

NCT00996346

Non-randomizedSingle-groupOpen-labelTreatment

Summary

Refractory soft tissue sarcoma remains a difficult malignancy to treat. The mammalian target of rapamycin (mTOR) is an enzyme that plays an important role in cancer cell survival. mTOR inhibitors, like temsirolimus, have shown activity in sarcoma. Irinotecan is a chemotherapy drug that has also been used to treat sarcoma. However, it is unknown whether combining these two drugs would result in improved efficacy with acceptable toxicity. Therefore, the goal of this phase I study is to determine the maximum tolerated dose (MTD) and toxicity profile of combination temsirolimus and irinotecan both administered intravenously on a weekly basis to refractory soft tissue sarcoma patients.

Timeline

Start
2009-10
Primary completion
2011-11
Completion
2013-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Irinotecan Small molecule 50 mg/m2 Intravenous
Subject Irinotecan Small molecule 80 mg/m2 Intravenous
Subject Temsirolimus Small molecule 15 mg Intravenous
Subject Temsirolimus Small molecule 20 mg Intravenous
Subject Temsirolimus Small molecule 25 mg Intravenous

Indications