drugset / Trial / NCT02655016

A Study of Niraparib (GSK3985771) Maintenance Treatment in Participants With Advanced Ovarian Cancer Following Response on Front-Line Platinum-Based Chemotherapy

NCT02655016 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study aims to assess efficacy of Niraparib (GSK3985771) as maintenance treatment in participants with Stage III or IV ovarian cancer. Participants must have completed front-line platinum based regimen with complete response (CR) or partial response (PR). Data collection for Secondary Outcome measures is ongoing and the approximate duration of the study will be 7 years.

Timeline

Start
2016-07-11
Primary completion
2019-05-17
Completion
2026-05-29

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo vs Niraparib; p <0.0001; Hazard Ratio (HR) 0.62 (95% CI 0.502 to 0.755); Log Rank; NCT02655016 ↗

release “The PRIMA study significantly improved PFS for patients treated with Zejula, regardless of biomarker status.” gsk.com ↗

release “The PRIMA study significantly improved PFS for patients treated with Zejula, regardless of biomarker status.” gsk.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Niraparib Small molecule 200 mg —
Subject Niraparib Small molecule 300 mg —

Indications