
UK-based pharmaceutical company AstraZeneca has announced that the National Institute for Health and Care Excellence (NICE) posted a positive recommendation …

The European Commission has awarded approval to AstraZeneca and MSDโs Lynparza (olaparib) for germline BRCA-mutated (gBRCAm) metastatic pancreatic cancer, with …

Lynparza (olaparib), the PARP inhibitor developed by AstraZeneca and MSD, has just secured recommendation for approval from the European Medicines …

Lynparza (olaparib), developed by AstraZeneca and MSD, has secured FDA approval when paired with bevacizumab as a first-line maintenance treatment …

AstraZeneca has confirmed that its PARP inhibitor Lynparza (olaparib) has been awarded orphan drug designation in Japan for the maintenance …

Newly revealed Phase 3 data has shown that AstraZenecaโs oral vascular endothelial growth factor receptor (VEGFR) inhibitor cediranib, when combined …

Following the recommendation of the tablet formulation of the drug for use on the NHS in England and Wales, news …

It has been announced that tablet form of Lynparza (olaparib), the PARP inhibitor developed by AstraZeneca and MSD, has secured …

The FDAโs Oncologic Drugs Advisory Committee (ODAC) has recommended the approval of AstraZeneca and Merckโs Lynparza (olaparib) to treat pancreatic …

NICE has given its recommendation for the routine use on the NHS in England and Wales of AstraZeneca and MSDโs …

New Phase 3 data has emerged on AstraZeneca and MSDโs Lynparza (olaparib), showing that the PARP inhibitor achieved its primary …

AstraZenecaโs PARP inhibitor Lynparza was successful in improving progression free survival in a Phase 3 trial of patients with metastatic …

NICE has published final guidance which approves AstraZenecaโs Lynparza (olaparib) for use on the NHS as a maintenance therapy for …

AstraZeneca and MSDโs jointly-developed therapy Lynparza (olaparib) has scored its third EU approval, the pair announced, with authorisation for the …

AstraZeneca and MSDโs Lynparza (olaparib) has received a positive opinion from the EMAโs Committee for Medicinal Products for Human Use …