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ASTRAZENECA WKN: 886455 ISIN: GB0009895292 Kürzel: AZN Forum: Aktien Thema: Hauptdiskussion
131,12 USD
+0,15 %+0,20
24. Dec, 23:10:00 Uhr,
Nasdaq OTC
Kommentare 2.737
oxanabanana,
23.07.2021 11:35 Uhr
0
23 July 2021
Results from the Canadian Immunization Research Network (CIRN) with support from Public Health Agency of Canada and the Canadian Institutes of Health Research, published as a pre-print, demonstrated one dose of Vaxzevria was 82% effective against hospitalisation or death caused by the Beta/Gamma variants of the SARS-CoV-2 virus.
oxanabanana,
22.07.2021 13:37 Uhr
0
https://www.reuters.com/article/uk-health-coronavirus-britain-vaccines-idUSKBN2ER2FO
oxanabanana,
22.07.2021 13:37 Uhr
0
Wednesday’s study found that two doses of Pfizer’s shot was 88% effective at preventing symptomatic disease from the Delta variant, compared to 93.7% against the Alpha variant, broadly the same as previously reported.
Two shots of AstraZeneca vaccine were 67% effective against the Delta variant, up from 60% originally reported, and 74.5% effective against the Alpha variant, compared to an original estimate of 66% effectiveness.
oxanabanana,
21.07.2021 22:39 Uhr
0
21 July 2021
AstraZeneca today completed the acquisition of Alexion Pharmaceuticals, Inc. (Alexion). The closing of the acquisition marks the Company’s entry into medicines for rare diseases and the beginning of a new chapter for AstraZeneca.
G
Gewehrbeifuss,
15.07.2021 13:13 Uhr
0
Lol die USA und die WHO werfen Pfizer/Biontech Geldgier vor und lehnen eine dritte "Booster"-Impfung von Pfizer/Biontech ab. 🤣😂
oxanabanana,
08.07.2021 8:09 Uhr
0
8 July 2021
AstraZeneca’s Biologics License Application (BLA) for tezepelumab has been accepted and granted Priority Review for the treatment of asthma from the US Food and Drug Administration (FDA). Tezepelumab is being developed by AstraZeneca in collaboration with Amgen.
oxanabanana,
08.07.2021 8:08 Uhr
0
Tezepelumab regulatory submission accepted and granted FDA Priority Review in the US for the treatment of patients with asthma
oxanabanana,
06.07.2021 10:37 Uhr
0
https://www.astrazeneca.com/media-centre/press-releases/2021/astrazeneca-alexion-transaction-cleared-in-the-eu.html
oxanabanana,
06.07.2021 10:36 Uhr
0
6 July 2021
AstraZeneca's proposed acquisition of Alexion Pharmaceuticals, Inc. (Alexion) has achieved an important step towards completion by having cleared the European Commission review.
oxanabanana,
29.06.2021 8:24 Uhr
2
Sie hebt schon gut ab. Seit Anfang März von 78 bis jetzt auf 100 ist doch ganz normal
Marin,
29.06.2021 0:06 Uhr
0
Ich hoffe das die jetzt langsam anhebt
Marin,
29.06.2021 0:05 Uhr
1
Das sind gute Nachrichten
oxanabanana,
28.06.2021 18:02 Uhr
0
Nirsevimab MEDLEY Phase II/III trial demonstrated favourable safety and tolerability profile in infants at high risk of RSV
28 June 2021
The MEDLEY Phase II/III trial evaluated the safety and tolerability of nirsevimab compared to Synagis (palivizumab) when given to infants at high risk of respiratory syncytial virus (RSV) entering their first RSV season.
oxanabanana,
28.06.2021 18:01 Uhr
0
Forxiga recommended for approval in the EU by CHMP for the treatment of patients with chronic kidney disease
28 June 2021
AstraZeneca’s Forxiga (dapagliflozin) has been recommended for approval in the European Union (EU) for the treatment of chronic kidney disease (CKD) in adults with and without type-2 diabetes (T2D).
oxanabanana,
28.06.2021 18:01 Uhr
0
AstraZeneca Appoints Dr. Susan Galbraith as Executive Vice President, Oncology Research & Development
28 June 2021
AstraZeneca today appointed Dr. Susan Galbraith to lead Oncology Research & Development from initial discovery through late-stage development. Her appointment follows the passing of José Baselga earlier this year. She will join the Company’s Senior Executive Team and report to Chief Executive Officer, Pascal Soriot.
oxanabanana,
28.06.2021 18:00 Uhr
0
Vaxzevria induced immunity for at least one year following a single dose and strong immune responses following either a late second dose or a third dose
28 June 2021
A sub-analysis from the Oxford-led COV001 and COV002 trials with Vaxzevria induced strong immune responses following either a prolonged second dose interval of up to 45 weeks or following a third boosting dose.
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