The Phase III PRIMA (ENGOT-OV26/GOG-3012) study showing that Zejula (niraparib) maintained a sustained and clinically meaningful progression-free survival (PFS) benefit as a maintenance therapy in patients with first-line ovarian cancer following a response to platinum-based chemotherapy, UK pharma major GSK (LSE: GSK) announced today.
Importantly, said GSK, this benefit was sustained across all biomarker subgroups, including BRCAm, HRd and HRp. Results from the updated efficacy analysis will be presented at the 2022 European Society for Medical Oncology (ESMO) Annual Meeting (September 9-13). Zejula was acquired by GSK along with its buy of US drugmaker Tesaro for $5.1 billion in 2018. The drug is already marketed and generate sales of £395 million in 2021, and is seen as one of GSK’s growth drivers.
After a median three and a half years follow up, this ad hoc analysis showed:
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