drugset / Trial / NCT00869050

Capecitabine and Temozolomide for Neuroendocrine Cancers

NCT00869050 ↗

Phase 2 Completed 41 enrolled Columbia University
NaSingle-groupOpen-labelTreatment

Summary

This phase II study is designed to assess whether treatment with capecitabine/temozolomide (CAP/TEM) is safe and effective in treating subjects with progressive, differentiated, metastatic neuroendocrine tumors (NET). The primary objective of the study is to determine the radiologic response rate to this regimen in progressive, metastatic, differentiated neuroendocrine cancers.

Timeline

Start
2005-08
Primary completion
2013-12
Completion
2014-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Capecitabine Small molecule 1500 mg/m2 Oral
Subject Temozolomide Small molecule 150 mg/m2 Oral
Subject Temozolomide Small molecule 200 mg/m2 Oral