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pharmaphorum 08/23/2019 04:50
AstraZeneca has bought a priority review voucher (PRV) from Swedish biotech Sobi for $95 million, but isn’t revealing just yet what it intends to use it for.
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FiercePharmaManufacturing 08/22/2019 10:00
But AstraZeneca has already been preparing for talks with the Chinese government to include roxadustat on the country’s National Reimbursement Drug List.
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ENDPOINTS 08/22/2019 08:47
An emboldened AstraZeneca splurges $95M on a priority review voucher.
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BioPharma Dive 08/21/2019 11:30
The trial, called NEPTUNE, paired AstraZeneca's approved checkpoint inhibitor Imfinzi with its experimental drug tremelimumab, testing the two against platinum-based chemo in previously untreated patients.
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STAT 08/21/2019 09:33
A combination of AstraZeneca’s (AZN) lung cancer drug Imfinzi and an experimental treatment failed to extend the lives of patients with stage 4 non-small cell lung cancer and high levels of gene mutations, Reuters reports.
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Benzinga 08/21/2019 09:04
What's Next AstraZeneca said it intends to do a deep analysis of the vast clinical and biomarker data from the trial to gain further insights to improve Immuno-oncology approaches for patients with metastatic NSCLC.
More from Benzinga: 08/21/2019 07:49
AstraZeneca Imfinzi combination fails advanced lung cancer study.
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Pharmafile 08/21/2019 06:10
New data have emerged illustrating that AstraZeneca’s anti-CTLA4 antibody Imfinzi (durvalumab) failed to meet its primary endpoint when used in combination with tremelimumab in the treatment of previously-untreated Stage IV (metastatic) non-small cell lung cancer (NSCLC), compared to standard-of-care (SoC) platinum-based chemotherapy. The study was performed in an all-comers population, with a primary analysis of patients with a high tumour mutational burden (TMB), meaning a higher number of mutations in the tumour’s DNA, potentially making it more visible to the immune system.
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PharmaTimes 08/21/2019 06:08
AstraZeneca has announced that its combination of Imfinzi (durvalumab) and tremelimumab has failed to hit its key target in a late-stage trial assessing its potential in patients with late-stage lung cancer.
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