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NEUTRALAstraZeneca's Koselugo approved in the US for adult NF1 patients with plexiform neurofibromas
The biopharmaceutical company has received US approval for its Koselugo drug to treat a rare genetic condition in adults.
AstraZeneca
13,820.00GBX
1.25%
Market Cap
214.25B
Volume
3.01M
151% of avg
P/E Ratio
1914.13
EPS (TTM)
7.22
Beta
0.17
Day Range
13,508.00p - 13,836.00p
52 Week Range
9,573.50p13,820.00p13,884.00p
13,820.00p
Upcoming Events
AZN
NEUTRALAstraZeneca Announces Major Shareholder Disclosure
The pharmaceutical company has received a notification from a major shareholder regarding their shareholding position.
AZN
NEUTRALAstraZeneca CFO Sells Shares
The CFO of the pharmaceutical company has sold a portion of their American Depositary Shares.
AZN
NEUTRALAstraZeneca Announces Director Share Transfer
The biopharmaceutical company announces its CEO has gifted shares to family members.
AZN
VERY GOODAstraZeneca Delivers Strong 9M 2025 Results, Beats Expectations
The biopharmaceutical company reported strong 9M 2025 results, with total revenue up 10% and core EPS up 15% compared to the prior year period, beating market expectations.
AZN
NEUTRALAstraZeneca Announces Director Appointment
The healthcare company has announced the appointment of a new non-executive director to its board.
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NEUTRALAstraZeneca's Koselugo approved in EU for rare genetic condition
The biopharmaceutical company has received EU approval for its Koselugo treatment for a rare genetic condition affecting the nerves.
AZN
NEUTRALAstraZeneca Receives EU Approval for Tezspire to Treat Chronic Rhinosinusitis with Nasal Polyps
The biopharmaceutical company has received European Commission approval for its Tezspire treatment for chronic rhinosinusitis with nasal polyps.
AZN
NEUTRALAstraZeneca's Tezspire Approved by FDA for Chronic Rhinosinusitis with Nasal Polyps
The biopharmaceutical company has received FDA approval for its Tezspire treatment for a chronic respiratory condition.
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NEUTRALAstraZeneca's Saphnelo Subcutaneous Formulation Recommended for EU Approval
The biopharmaceutical company received a positive CHMP opinion for a subcutaneous version of its lupus drug Saphnelo, which could provide patients with a more convenient administration option.