drugset / Trial / NCT00819221

AZD2281 in Combination With Liposomal Doxorubicin in Advanced Solid Tumours

NCT00819221

Phase 1 Terminated 44 enrolled AstraZeneca
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The study will be an open label, multicenter, dose finding study. Depending on the tolerated dose up to 7 dose levels will be explored in this study, approximately 33 patients (21-54 depending on number of cohorts) may be enrolled into this study. Three patients will be initially dosed in each cohort. The primary objective of this study is to determine the recommended dose (RD) of twice daily oral doses of AZD2281 either as intermittent therapy for 7 days out of a 28-day schedule or given continuously, administered in combination with liposomal doxorubicin to patients with advanced solid tumors.

Timeline

Start
2009-01-05
Primary completion
2011-11-30
Completion
2021-12-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Doxorubicin Other / unclassified 40 mg/m2
Subject Olaparib Small molecule 50 mg Oral
Subject Olaparib Small molecule 400 mg Oral

Indications