This page shows the latest HER2-negative breast cancer news and features for those working in and with pharma, biotech and healthcare.
The anti-cancer medicine will now be routinely available for adults with HER2-negative, high-risk early breast cancer who have inherited faults in their BRCA1 or BRCA2 genes, after surgery ... NICE estimates that 300 adults with breast cancer will now be
The decision to remove the previous 20% Ki-67 score requirement for patient selection means that those with HR-positive, HER2-negative early breast cancer can now be identified solely based ... Although the prognosis for HR-positive, HER2-negative early
The authorisation is specifically for adult patients with unresectable locally advanced or metastatic HR-positive, HER2-negative (HR+/HER2-) breast cancer who have received endocrine-based therapy and at least two ... for people with metastatic
Gilead’s supplemental Biologics Licence Application for Trodelvy (sacituzumab govitecan-hziy) for pre-treated hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR+/HER2-) metastatic breast cancer patients has ... HR+/HER2-
Food and Drug Administration (FDA) for the treatment of adult patients with metastatic castration-resistant prostate cancer (mCRPC), AZ announced. ... The announcement follows the European Commission’s approval of Lynparza earlier this month for the
HR+/HER2- breast cancer accounts for around 70% of all new cases, or nearly 400, 000 diagnoses worldwide each year. ... HR+/HER2- breast cancer is the most common type of breast cancer, accounting for around 70% of all new cases, or nearly 400, 000
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The drug has so far gained approval for use in patients with germline BRCA1/2-mutated (gBRCAm), human epidermal growth factor receptor 2 (HER2)- negative locally advanced or metastatic breast cancer, ... That’s a measure of its heightened ambitions in
Innovative health revenue increased 4% to $8.47bn, lifted by sales of blood thinner Eliquis and breast cancer drug Ibrance outside the US, among others. ... In October the FDA also approved Talzenna (talazoparib), a new treatment of deleterious or
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