drugset / Trial / NCT01968213

Phase 3 Study of Rucaparib as Switch Maintenance After Platinum in Relapsed High Grade Serous or Endometrioid Ovarian Cancer (ARIEL3)

NCT01968213 ↗

RandomizedParallel-groupDouble-blindTreatment

Summary

Patients enrolled into this study will be stratified into 3 groups based on gene mutations identified in their tumor tissue. The purpose of this study is to evaluate patient response to maintenance treatment with rucaparib versus placebo. Response to treatment will be analyzed based on homologous recombination (HR) status of tumor samples.

Timeline

Start
2014-04-07
Primary completion
2017-04-01
Completion
2022-07-07

Outcome

Met primary endpoint

registry analysis (superiority test); Rucaparib 600 mg Tablets vs Placebo Tablets; p <0.0001; Cox Proportional Hazard 0.365 (95% CI 0.295 to 0.451); Regression, Cox NCT01968213 ↗

paper In the intention-to-treat population, it was 10·8 months (8·3-11·4) versus 5·4 months (5·3-5·5; 0·36 (0·30-0·45]; p<0·0001). PMID 28916367 ↗

paper Across all primary analysis groups, rucaparib significantly improved progression-free survival PMID 28916367 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Rucaparib Small molecule 600 mg Oral