drugset / Trial / NCT00635323

Safety And Efficacy Of Irinotecan Plus Capecitabine As First-Line Treatment In Asian Subjects With Hepatocellular Carcinoma

NCT00635323 ↗

Phase 2 Completed 73 enrolled Pfizer
Non-randomizedSingle-groupOpen-labelTreatment

Summary

To evaluate the safety and efficacy of irinotecan and capecitabine in Asian subjects with inoperable hepatocellular carcinoma.

Timeline

Start
2002-11
Primary completion
—
Completion
2005-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Capecitabine Small molecule 1000 mg/m2 Oral
Subject Irinotecan Small molecule 200 mg/m2 Intravenous
Subject Irinotecan Small molecule 250 mg/m2 Intravenous