Trial Profile

Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of Niraparib Maintenance Treatment in Patients With Advanced Ovarian Cancer Following Response on Front-Line Platinum-Based Chemotherapy

Status: Active, no longer recruiting

Phase of Trial: Phase III

Latest Information Update: 26 Mar 2026

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At a glance

19 Mar 2026 According to the Myriad Genetics media release, the U.S. Food and Drug Administration (FDA) has approved the MyChoice CDx Test as the Companion Diagnostic (CDx) for Zejula (niraparib), a PARP inhibitor from GSK, for patients with advanced ovarian cancer, This approval is based on final data from the PRIMA trial.
10 Mar 2026 Planned End Date changed from 30 Mar 2026 to 29 May 2026.
27 Jan 2026 Planned End Date changed from 30 Jan 2026 to 30 Mar 2026.

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