drugset / Trial / NCT02753881

Pharmacokinetics of Doxorubicin in cTACE of Liver Cancer

NCT02753881 ↗

Phase 1 Completed 30 enrolled Yale University
Non-randomizedParallel-groupOpen-labelTreatment

Summary

Patients with primary and secondary liver cancer may participate in this study. The purpose is to perform an analysis of the effects of doxorubicin and its metabolite doxorubicinol on the body (doxorubicin pharmacokinetics ) after conventional transarterial chemoembolization (cTACE). cTACE is a procedure in which chemotherapy drugs are injected, followed by an injection of small beads to block the tumor-feeding arteries. Doxorubicin is a chemotherapeutic agent used in the cTACE procedure. This study will examine doxorubicin pharmacokinetics in patients who: 1) receive whole liver cTACE; and 2) receive super-selective CTACE (i.e., delivered in close proximity to the tumor).

Timeline

Start
2015-11
Primary completion
2019-12
Completion
2019-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator Doxorubicin Other / unclassified 50 mg Other

Indications