Encouraging new data of relevance to Global public health crisis, presented at 25th European Congress of Clinical Microbiology and Infectious Diseases (ECCMID)
Det finansiella resultatet för kvartal 1 2015 ger stöd åt upprepad helårsprognos för 2015.
oTotala intäkter (definierat som produktförsäljning och intäkter från externa samarbeten1) ökade med 1% i fasta valutakurser 2 (CER) till 6 057 MUSD (Q1 2014: 6 460 MUSD)
oVinst per aktie för kärnverksamheten (Core EPS) minskade med 3% till1,08 USD i takt med att vi fortsätter att investera i att uppn
AstraZeneca and MedImmune, the Company’s global biologics research and development arm, today announced that they have entered into an exclusive collaboration agreement with Celgene Corporation, a global leader in haematological cancers, for the development and commercialisation of MEDI4736
AstraZeneca and MedImmune, the Company’s global biologics research and development arm, today announced that they have entered into a collaboration to accelerate and broaden the development of Innate Pharma SA’s proprietary anti-NKG2A antibody
Idag tilldelas Berglind Libungans, verksam vid enheten för kardiologi, Sahlgrenska Universitetssjukhuset i Göteborg ett forskningsstipendium på 120 000 kr.
AstraZeneca and Bina Technologies, Inc., a member of the Roche Group, today announced that they have entered into an agreement for AstraZeneca to become the first member to join the Bina Alliance Programme
Uppdaterade data som presenterades vid European Lung Cancer Conference 2015 visar en fördröjning av tumörprogression på över ett år
AstraZeneca today announced that the US Food and Drug Administration has granted Orphan Drug Designation for the MEK inhibitor selumetinib, for the treatment of uveal melanoma.
AstraZeneca today announced that MedImmune, its global biologics research and development arm, has entered into a collaboration to conduct clinical trials in immuno-oncology with Immunocore Limited, a privately-held UK-based biotechnology company.
AstraZeneca meddelar i dag att den amerikanska läkemedelsmyndigheten (Food and Drug Administration, FDA) har beviljat särläkemedelsstatus åt den monoklonala anti-CTLA-4-antikroppen tremelimumab för behandling av malignt mesoteliom.
AstraZeneca today announced that the US Food and Drug Administration (FDA) Endocrinologic and Metabolic Drugs Advisory Committee (EMDAC) voted 13to 1(1 abstained; 15 total votes) that the results of the Saxagliptin Assessment of Vascular Outcomes Recorded in Patients with
•More than 60 scientific abstracts to be featured at the meeting, highlighting the breadth and depth of AstraZeneca’s oncology pipeline and ability to test a range of small molecule and biologic combinations.
Nu finns AstraZenecas läkemedel Moventig® (naloxegol) tillgängligt i Sverige, som första land i Europa. Läkemedlet är avsett för att behandla förstoppning orsakad av smärtlindrande läkemedel innehållande opioider hos vuxna patienter som upplevt otillräcklig effekt av laxermedel
AstraZeneca today announced that it has entered into a five-year research collaboration with the Harvard Stem Cell Institute (HSCI) to adapt a technique that creates human beta cells from stem cells for use in screens of AstraZeneca’s compound library in the search for new treatments for diabetes.
AstraZeneca meddelar idag att man ingått ett samarbetsavtal med Daiichi Sankyo Inc. avseende marknadsföring av MOVANTIK™ (naloxegol) i USA.
AstraZeneca today announced positive top-line results from the Phase III PINNACLE programme, which included two pivotal 24-week studies (PINNACLE 1 and PINNACLE 2) to investigate the potential of PT003 to improve lung function in patients with Chronic Obstructive Pulmonary Disease (COPD).
Data från en studie med 21 000 patienter presenterades på den 64:e årliga vetenskapliga kongressen som hålls av American College of Cardiology och publicerades parallellt i New England Journal of Medicine
AstraZeneca today announces an update to the presentation of its Statement of Comprehensive Income, which will see revenue from externalisation becoming more visible to enhance transparency for investors. The change is effective from 1 January 2015 and will be reported as part of the Company’s first quarter financial results on 24 April 2015.
AstraZeneca today announced it will participate in the US Food and Drug Administration (FDA) Endocrinologic and Metabolic Drugs Advisory Committee meeting on 14 April 2015 to discuss the results of the Saxagliptin Assessment of Vascular Outcomes Recorded in Patients with Diabetes Mellitus (SAVOR) trial for ONGLYZA® (saxagliptin) and Kombiglyze® XR (saxagliptin and metformin HCI extended-release).
Acquisition strengthens AstraZeneca’s aclidinium respiratory franchise and adds immediate revenues with long-term growth potential