drugset / Trial / NCT00628251

Dose-finding Study Comparing Efficacy and Safety of a PARP Inhibitor Against Doxil in BRCA+ve Advanced Ovarian Cancer

NCT00628251 ↗

Phase 2 Completed 97 enrolled AstraZeneca
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of the study is to compare the efficacy and safety of 2 doses of drug AZD2281 against liposomal doxorubicin to see which is effective and well tolerated in treating patients with measurable BRCA1- or BRCA2-positive advanced ovarian cancer and who have failed previous platinum therapy.

Timeline

Start
2008-07-30
Primary completion
2009-09-15
Completion
2018-09-19

Outcome

Missed primary endpoint

registry Olaparib 200 mg bd vs Olaparib 400 mg bd vs Liposomal Doxorubicin; p = 0.6604; Hazard Ratio (HR) 0.88 (95% CI 0.51 to 1.56); Regression, Cox NCT00628251 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Doxorubicin Other / unclassified 50 mg/m2 Intravenous
Subject Olaparib Small molecule 200 mg Oral
Subject Olaparib Small molecule 400 mg Oral

Indications