This page shows the latest Zejula news and features for those working in and with pharma, biotech and healthcare.
GlaxoSmithKline (GSK) has announced that the National Institute for Health and Care Excellence (NICE) has issued a Final Appraisal Determination (FAD) recommending the use of Zejula (niraparib) on the NHS. ... Zejula is recommended as a therapy option
GSK gained dostarlimab from its $5.1bn acquisition of cancer specialist Tesaro, as well as PARP inhibitor Zejula (niraparib), which is approved across a number of indications including ovarian, fallopian tube
That includes GlaxoSmithKline’s (GSK) Zejula (niraparib) and Clovis Oncology’s Rubraca (rucaparib). ... GSK’s Zejula is more of a threat to Lynparza in the ovarian cancer market, with both companies revealing positive results for the respective
As a result of the Tesaro deal, GSK gained the rights to PARP inhibitor treatment Zejula, a particularly important drug in the company’s growing oncology portfolio. ... Although the PARP category is currently dominated by AstraZeneca and Merck
Seeks approval in advanced ‘all-comer’ ovarian cancer population. GlaxoSmithKline is on course to broaden the label of its PARP inhibitor Zejula, after announcing yesterday that the US Food and Drug ... GSK is seeking approval for Zejula (niraparib)
GSK took full ownership of the therapy in 2018. GSK’s push into cancer has also included its $5.1bn acquisition of Tesaro, which brought in PARP inhibitor Zejula (niraparib). ... Barron has said Zejula is one of three that he expects to drive the
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Prior to GSK, Dr Carpenter was at Merck, where he led the development of Tesaro’s Zejula.
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11. European Medicines Agency. Zejula. Available at: https://www.ema.europa.eu/en/medicines/human/EPAR/zejula. Accessed April 2019.
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