Astrazeneca

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Enhertu gets breakthrough tag in HER2-low breast cancer

AstraZeneca and Daiichi Sankyo have claimed a fifth breakthrough designation from the FDA for Enhertu, shortly after showing the drug extended survival in patients with HER2-low metastatic

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AstraZeneca Amenities Building - Mississauga - Sept 2005
Non exclusive, unlimited time license for print & web to WZMH Architects

AZ closes on FDA verdict on tremelimumab in liver cancer

AstraZeneca's anti-CTLA4 antibody tremelimumab is moving closer to what once looked like an extremely unlikely regulatory approval, after a string of negative trial results.

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FDA starts speedy review of Enhertu in lung cancer

AstraZeneca and Daiichi Sankyo should only have to wait for six months to hear from the FDA if it will approve their HER2 drug Enhertu for non-small cell lung cancer (NSCLC) and add to its

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GSK goes for gold as FDA starts review of daprodustat

GlaxoSmithKline says the FDA has started its review of daprodustat for anaemia associated with chronic kidney disease (CKD), as it strives to succeed where two other rivals in the HIF-PHI c

News

Seagen wins Enhertu patent dispute with Daiichi Sankyo

A US jury has decided that Daiichi Sankyo and AstraZeneca's breast cancer drug Enhertu infringes a patent held by US biotech Seagen, awarding almost $42 million in damages.

News

FDA restricts GSK's Xevudy due to lower efficacy against BA....

GlaxoSmithKline and Vir's Xevudy has become the latest COVID-19 antibody therapy to have its use restricted by the FDA as a result of waning activity against new variants of the virus.

Enhertu gets breakthrough tag in HER2-low breast cancer

AZ closes on FDA verdict on tremelimumab in liver cancer

FDA starts speedy review of Enhertu in lung cancer

GSK goes for gold as FDA starts review of daprodustat

Seagen wins Enhertu patent dispute with Daiichi Sankyo

FDA restricts GSK's Xevudy due to lower efficacy against BA....

Court sides with EU on decision to revoke Ocaliva's license

Coming soon: The Life Sciences Industry Report 2025 – insigh...

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