PARP inhibitors could exploit weaknesses in a range of cancers
Drug type could offer a new approach to treating a number of cancers with PBRM1 mutations
Read Moreby Lucy Parsons | Apr 23, 2021 | News | 0
Drug type could offer a new approach to treating a number of cancers with PBRM1 mutations
Read Moreby Selina McKee | Nov 2, 2020 | News | 0
Zejula is the first PARP inhibitor to be approved as monotherapy in the EU for patients with platinum-responsive advanced ovarian cancer, regardless of biomarker status
Read Moreby Anna Smith | Jun 24, 2019 | News | 0
The indication is for patients with inherited BRCA-mutated locally advanced or metatastatic breast cancer.
Read Moreby Anna Smith | Apr 30, 2019 | News | 0
The positive opinion is based on data from the pivotal Phase III SOLO-1 trial.
Read Moreby Selina McKee | Jun 5, 2018 | News | 0
Clovis Oncology is seeking to expand use of its PARP inhibitor Rubraca in Europe to include maintenance treatment of certain adults with recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer.
Read Moreby Selina McKee | Apr 9, 2018 | News | 0
Clovis’ PARP inhibitor Rubraca has won a second US approval, as maintenance treatment for patients with recurrent ovarian cancer.
Read Moreby Selina McKee | Apr 4, 2018 | News | 0
MSD and AstraZeneca’s Lynparza will be the first PARP inhibitor to be reviewed in Europe for the treatment of breast cancer, after the European Medicines Agency validated the drug’s marketing application in this setting.
Read Moreby Selina McKee | Jan 4, 2018 | News | 0
AstraZeneca has expanded its agreement with US group Myriad Genetics to identify women with advanced ovarian cancer most likely to benefit from its medicines.
Read Moreby Selina McKee | Jun 19, 2017 | News | 0
UK-based scientists have developed a new three-in-one blood test able to identify the patients with advanced prostate cancer most likely to benefit from PARP inhibitors, with the potential to ‘transform’ treatment of the disease.
Read Moreby Selina McKee | Apr 20, 2017 | News | 0
AbbVie’s experimental PARP inhibitor veliparib has failed to meet key targets in two late-stage studies testing its potential in lung and breast cancer.
Read Moreby Selina McKee | Feb 20, 2017 | News | 0
A late-stage study of AstraZeneca’s PARP inhibitor Lynparza in patients with HER2-negative metastatic breast cancer who also carry BRCA1 or BRCA2 mutations has its primary target of boosting progression-free survival (PFS).
Read Moreby Selina McKee | Nov 7, 2016 | News | 0
AbbVie’s experimental lung cancer drug veliparib has picked up Orphan Drug status in the US, opening the door to potential tax credits, waived fees, protocol assistance and exclusivity benefits.
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