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Home Featured

Singapore Authorises New Ovarian Cancer Treatment By GSK

Content Team by Content Team
5th July 2022
in Featured, Manufacturing, Middle East and South Asia, News
GSK commences phase III study of Benlysta and rituximab combination in systemic lupus erythematosus

Note* - All images used are for editorial and illustrative purposes only and may not originate from the original news provider or associated company.

The oral, once-daily Zejula (niraparib) tablet, a first-line and recurrent upkeep care for women with advanced epithelial high-grade ovarian, fallopian tube, or primary peritoneal cancer who are in full or partial remission after platinum-based chemotherapy, has been approved by the Health Sciences Authority, according to a statement from GlaxoSmithKline (GSK) Singapore.

Regardless of whether a patient has a BRCA mutation, Zejula is now the only poly (ADP-ribose) polymerase (PARP) inhibitor licenced in Singapore to be used as a single therapy for patients with advanced and recurrent ovarian cancer.

As of March 2022, Zejula is accessible for the first ovarian cancer (PRIMA) in 44 nations and 2 Special Administration Regions. Zejula is also being tested against a variety of tumour types and in combination with a number of different treatments. Notably, it is now undergoing testing in a Phase III clinical research called ZEST to examine its potential for treating individuals with breast cancers that have the specialised treatment needs of triple-negative breast cancer (TNBC) or BRCAm HER2- breast cancer.

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