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2 November 2020 | By Hannah Balfour (European Pharmaceutical Review)
The European Commission (EC) has approved Zejula, the first PARP-inhibitor monotherapy approved in the EU for patients with advanced ovarian cancer, regardless of their biomarker status.
26 February 2020 | By Hannah Balfour (European Pharmaceutical Review)
The developers of Zejula (niraparib) have announced the FDA will assess the sNDA application under the Real-Time Oncology Review (RTOR) pilot programme.
22 January 2020 | By Victoria Rees (European Pharmaceutical Review)
The pharmaceutical industry saw some notable mergers and acquisitions in 2019; this article lists the top 10 by transaction size.
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