drugset / Trial / NCT00952497

A Study of Telatinib in Combination With Chemotherapy in Subjects With Advanced Gastric Cancer

NCT00952497 ↗

Phase 2 Completed 48 enrolled ACT Biotech, Inc
NaSingle-groupOpen-labelTreatment

Summary

The objectives of this study are to evaluate the anti-tumor activity, safety, and tolerability of telatinib when used in combination with chemotherapy (capecitabine and cisplatin) as first-line therapy in subjects with advanced gastric cancer. The primary objective is to assess progression free survival (PFS) in subjects receiving telatinib in combination with chemotherapy (capecitabine and cisplatin). The secondary objectives are to assess overall survival, overall response rate, safety and tolerability, pharmacokinetics and biomarkers.

Timeline

Start
2009-06
Primary completion
2011-10
Completion
2012-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Telatinib Small molecule — Oral
Background Capecitabine Small molecule 1000 mg/m2 —
Background Cisplatin Other / unclassified 80 mg/m2 —

Indications