drugset / Trial / NCT00065468

Study Evaluating Interferon And CCI-779 In Advanced Renal Cell Carcinoma

NCT00065468 ↗

Phase 3 Completed 626 enrolled Pfizer
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of this study is efficacy. The primary efficacy endpoint of this study is a comparison of the overall survival of subjects treated with CCI-779 \[Temsirolimus\], administered intravenously \[IV\] once weekly and the combination of CCI-779, administered IV once weekly with Interferon Alfa \[IFN alfa\] subcutaneously \[SC\] three times per week \[TIW\], compared with the overall survival of subjects treated with IFN alfa (SC TIW) alone, in poor-prognosis subjects with advanced RCC.

Timeline

Start
2003-07
Primary completion
2006-06
Completion
2011-03

Outcome

Mixed primary results

paper temsirolimus alone had longer overall survival (hazard ratio for death, 0.73; 95% confidence interval [CI], 0.58 to 0.92; P=0.008) PMID 17538086 ↗

paper Overall survival in the combination-therapy group did not differ significantly from that in the interferon group (hazard ratio, 0.96; 95% CI, 0.76 to 1.20; P=0.70). PMID 17538086 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Temsirolimus Small molecule 15 mg Intravenous
Subject Temsirolimus Small molecule 25 mg Intravenous
Subject interferon alfa Protein / enzyme biologic 6e+06 iu Subcutaneous
Subject interferon alfa Protein / enzyme biologic 1.8e+07 iu Subcutaneous

Indications