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AstraZeneca PLC (AZN.L)

LSE - LSE Delayed price. Currency in GBp (0.01 GBP)
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12,206.00+144.00 (+1.19%)
As of 02:25PM BST. Market open.
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Previous close12,062.00
Open12,194.00
Bid12,206.00 x 0
Ask12,210.00 x 0
Day's range12,054.00 - 12,270.00
52-week range9,461.00 - 12,488.00
Volume473,537
Avg. volume2,999,762
Market cap189.22B
Beta (5Y monthly)0.19
PE ratio (TTM)37.91
EPS (TTM)3.22
Earnings date25 July 2024
Forward dividend & yield2.28 (1.89%)
Ex-dividend date22 Feb 2024
1y target est125.61
  • Business Wire

    AstraZeneca unveils latest research across key respiratory and immune-mediated diseases at ATS 2024 showcasing strength of its broad pipeline and portfolio

    WILMINGTON, Del., May 01, 2024--AstraZeneca will showcase new clinical and real-world data across its leading inhaled, biologic and early science respiratory portfolio at the American Thoracic Society (ATS) International Conference, in San Diego, CA from May 17 - 22, 2024. The company will present 59 abstracts, including 12 late-breaking posters, with a focus on unmet needs in chronic obstructive pulmonary disease (COPD), severe asthma and eosinophilic granulomatosis with polyangiitis (EGPA), as

  • Insider Monkey

    AstraZeneca PLC (NASDAQ:AZN) Q1 2024 Earnings Call Transcript

    AstraZeneca PLC (NASDAQ:AZN) Q1 2024 Earnings Call Transcript April 25, 2024 AstraZeneca PLC misses on earnings expectations. Reported EPS is $1.03 EPS, expectations were $1.22. AstraZeneca PLC isn’t one of the 30 most popular stocks among hedge funds at the end of the third quarter (see the details here). Operator: Good morning to those joining […]

  • Business Wire

    ENHERTU® (fam-trastuzumab deruxtecan-nxki) improved PFS in HER2-low and ultralow

    WILMINGTON, Del., April 29, 2024--Positive high-level results from the DESTINY-Breast06 Phase III trial showed that ENHERTU® (fam-trastuzumab deruxtecan-nxki) demonstrated a statistically significant and clinically meaningful improvement in progression-free survival (PFS) compared to standard-of-care chemotherapy in the primary trial population of patients with HR-positive, HER2-low (IHC 1+ or 2+/ISH-) metastatic breast cancer following one or more lines of endocrine therapy.