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2025-04-29 08:00 Kvartalsrapport 2025-Q1
2025-02-06 08:00 Bokslutskommuniké 2024
2024-11-12 - Kvartalsrapport 2024-Q3
2024-08-08 - X-dag halvårsutdelning AZN 77.600002
2024-07-25 - Kvartalsrapport 2024-Q2
2024-04-25 - Kvartalsrapport 2024-Q1
2024-04-11 - Årsstämma
2024-02-22 - X-dag halvårsutdelning AZN 20.65
2024-02-08 - Bokslutskommuniké 2023
2023-11-09 - Kvartalsrapport 2023-Q3
2023-08-10 - X-dag halvårsutdelning AZN 9.64
2023-07-28 - Kvartalsrapport 2023-Q2
2023-04-27 - Årsstämma
2023-04-27 - Kvartalsrapport 2023-Q1
2023-02-23 - X-dag halvårsutdelning AZN 20.69
2023-02-09 - Bokslutskommuniké 2022
2022-11-10 - Kvartalsrapport 2022-Q3
2022-08-11 - X-dag halvårsutdelning AZN 9.49
2022-07-29 - Kvartalsrapport 2022-Q2
2022-04-29 - Årsstämma
2022-04-29 - Kvartalsrapport 2022-Q1
2022-02-24 - X-dag halvårsutdelning AZN 1.97
2022-02-10 - Bokslutskommuniké 2021
2021-11-12 - Kvartalsrapport 2021-Q3
2021-08-12 - X-dag halvårsutdelning AZN 7.72
2021-07-29 - Kvartalsrapport 2021-Q2
2021-05-11 - Årsstämma
2021-04-30 - Kvartalsrapport 2021-Q1
2021-02-25 - X-dag halvårsutdelning AZN 15.76
2021-02-11 - Bokslutskommuniké 2020
2020-11-05 - Kvartalsrapport 2020-Q3
2020-08-13 - X-dag halvårsutdelning AZN 7.87
2020-07-30 - Kvartalsrapport 2020-Q2
2020-04-29 - Årsstämma
2020-04-29 - Kvartalsrapport 2020-Q1
2020-02-27 - X-dag halvårsutdelning AZN 18.32
2020-02-14 - Bokslutskommuniké 2019
2019-10-24 - Kvartalsrapport 2019-Q3
2019-08-08 - X-dag halvårsutdelning AZN 8.49
2019-07-25 - Kvartalsrapport 2019-Q2
2019-04-26 - Årsstämma
2019-04-26 - Kvartalsrapport 2019-Q1
2019-02-28 - X-dag halvårsutdelning AZN 17.46
2019-02-14 - Bokslutskommuniké 2018
2018-11-08 - Kvartalsrapport 2018-Q3
2018-08-09 - X-dag halvårsutdelning AZN 7.92
2018-07-26 - Kvartalsrapport 2018-Q2
2018-05-18 - Årsstämma
2018-05-18 - Kvartalsrapport 2018-Q1
2018-02-15 - X-dag halvårsutdelning AZN 14.97
2018-02-02 - Bokslutskommuniké 2017
2017-11-09 - Kvartalsrapport 2017-Q3
2017-08-10 - X-dag halvårsutdelning AZN 7.4
2017-07-27 - Kvartalsrapport 2017-Q2
2017-04-27 - Årsstämma
2017-04-27 - Kvartalsrapport 2017-Q1
2017-02-16 - X-dag halvårsutdelning AZN 16.57
2017-02-02 - Bokslutskommuniké 2016
2016-11-10 - Kvartalsrapport 2016-Q3
2016-08-11 - X-dag halvårsutdelning AZN 7.81
2016-07-28 - Kvartalsrapport 2016-Q2
2016-04-29 - Årsstämma
2016-04-29 - Kvartalsrapport 2016-Q1
2016-02-18 - X-dag halvårsutdelning AZN 16.26
2016-02-04 - Bokslutskommuniké 2015
2015-11-05 - Kvartalsrapport 2015-Q3
2015-08-13 - X-dag halvårsutdelning AZN 7.71
2015-07-30 - Kvartalsrapport 2015-Q2
2015-04-24 - Årsstämma
2015-04-24 - Kvartalsrapport 2015-Q1
2015-02-19 - X-dag halvårsutdelning AZN 15.62
2015-02-05 - Bokslutskommuniké 2014
2014-11-06 - Kvartalsrapport 2014-Q3
2014-08-13 - X-dag halvårsutdelning AZN 6.2
2014-07-31 - Kvartalsrapport 2014-Q2
2014-04-24 - Årsstämma
2014-04-24 - Kvartalsrapport 2014-Q1
2014-02-19 - X-dag halvårsutdelning AZN 129.777777
2014-02-06 - Bokslutskommuniké 2013
2013-10-31 - Kvartalsrapport 2013-Q3
2013-08-14 - X-dag halvårsutdelning AZN 65.777779
2013-08-01 - Kvartalsrapport 2013-Q2
2013-08-01 - Analytiker möte 2013
2013-04-25 - Årsstämma
2013-04-25 - Kvartalsrapport 2013-Q1
2013-02-13 - X-dag halvårsutdelning AZN 133.888888
2013-01-31 - Bokslutskommuniké 2012
2012-10-25 - Kvartalsrapport 2012-Q3
2012-10-25 - Analytiker möte 2012
2012-08-08 - X-dag halvårsutdelning AZN 64.555556
2012-07-26 - Kvartalsrapport 2012-Q2
2012-04-26 - Årsstämma
2012-04-26 - Kvartalsrapport 2012-Q1
2012-02-15 - X-dag halvårsutdelning AZN 137.333333
2012-02-02 - Bokslutskommuniké 2011
2011-10-27 - Kvartalsrapport 2011-Q3
2011-08-03 - X-dag halvårsutdelning AZN 57.666665
2011-07-28 - Kvartalsrapport 2011-Q2
2011-04-28 - Årsstämma
2011-04-28 - Kvartalsrapport 2011-Q1
2011-02-02 - X-dag halvårsutdelning AZN 129.666662
2011-01-27 - Bokslutskommuniké 2010
2010-10-28 - Kvartalsrapport 2010-Q3
2010-08-04 - X-dag halvårsutdelning AZN 5.12
2010-07-29 - Kvartalsrapport 2010-Q2
2010-04-29 - Kvartalsrapport 2010-Q1
2010-02-03 - X-dag halvårsutdelning AZN 12.43
2010-01-28 - Bokslutskommuniké 2009
2009-10-29 - Kvartalsrapport 2009-Q3
2009-08-05 - X-dag halvårsutdelning AZN 4.41
2009-07-30 - Kvartalsrapport 2009-Q2
2009-04-30 - Årsstämma
2009-04-30 - Kvartalsrapport 2009-Q1
2009-02-04 - X-dag halvårsutdelning AZN 12.02
2008-08-06 - X-dag halvårsutdelning AZN 3.34
2008-02-06 - X-dag halvårsutdelning AZN 8.61
2007-08-08 - X-dag halvårsutdelning AZN 3.49
2007-02-07 - X-dag halvårsutdelning AZN 8.6
2006-08-09 - X-dag halvårsutdelning AZN 3.6
2006-02-08 - X-dag halvårsutdelning AZN 7.02
2005-08-10 - X-dag halvårsutdelning AZN 2.99
2005-02-09 - X-dag halvårsutdelning AZN 4.497
2004-08-11 - X-dag halvårsutdelning AZN 2.2
2004-02-18 - X-dag halvårsutdelning AZN 3.91
2003-08-20 - X-dag halvårsutdelning AZN 2.07
2003-02-19 - X-dag halvårsutdelning AZN 3.99
2002-08-21 - X-dag halvårsutdelning AZN 2.21
2002-02-20 - X-dag halvårsutdelning AZN 5.01
2001-08-22 - X-dag halvårsutdelning AZN 2.44
2001-02-21 - X-dag halvårsutdelning AZN 4.49
2000-09-04 - X-dag halvårsutdelning AZN 2.1
2000-03-08 - X-dag halvårsutdelning AZN 4.01
1999-09-06 - X-dag halvårsutdelning AZN 1.89
1999-04-01 - Split AZN 1:0.5045
1997-05-26 - Split AZN 1:2
1993-06-14 - Split AZN 1:5
1987-06-04 - Split AZN 1:2

Beskrivning

LandStorbritannien
ListaLarge Cap Stockholm
SektorHälsovård
IndustriLäkemedel & Handel
AstraZeneca är ett globalt läkemedelsbolag med fokus på forskning, utveckling och marknadsföring av receptbelagda läkemedel, primärt för behandling av sjukdomar inom terapiområdena som berör andningsvägar, hjärta/kärl/metabolism och cancer. Utöver huvudverksamheten är bolaget även aktiva inom autoimmunitet, neurovetenskap och infektion. AstraZeneca är verksamt inom samtliga globala regioner och har sitt huvudkontor i Cambridge, Storbritannien.
2024-10-10 08:01:10

Clinical and real-world data will reinforce the long-term safety and efficacy profiles of Ultomiris and Soliris and highlight the potential for sustained treatment to minimise steroid use.

Alexion, AstraZeneca Rare Disease, will present data from its leading generalised myasthenia gravis (gMG) portfolio at the American Association of Neuromuscular & Electrodiagnostic Medicine (AANEM) Annual Meeting and the Myasthenia Gravis Foundation of America (MGFA) Scientific Session taking place in Savannah, GA, 15 to 18 October 2024.

The company will present 11 abstracts, spanning clinical and real-world data, which add to the extensive body of evidence supporting the safety and efficacy of Ultomiris (ravulizumab) and Soliris (eculizumab) in treating anti-acetylcholine receptor (AChR) antibody-positive (Ab+) gMG, and offer new insights to inform clinical practice.

Christophe Hotermans, Senior Vice President, Head of Global Medical Affairs, Alexion, said: "We are pleased to present continued positive results for Ultomiris and Soliris in gMG, which showcase their potential to improve medical outcomes and the quality of life for patients. Alexion's data at the AANEM Annual Meeting and the MGFA Scientific Session will reinforce the benefits of sustained treatment, including reductions in the use of corticosteroids and the potential to achieve minimal symptom expression, supporting clinical decision-making and care."

Further evidence supporting Ultomiris and Soliris as steroid-sparing therapies

At the MGFA Scientific Session an analysis of global gMG registry data will demonstrate a reduced oral corticosteroid (OCS) burden in adults treated with Soliris or Ultomiris. Oral corticosteroid doses also continued to decrease from treatment initiation to last dose assessed in patients who transitioned from Soliris to Ultomiris. Following treatment, there was a greater number of patients who transitioned from a higher dose to a lower dose of daily OCS.

Two encore poster presentations at the AANEM Annual Meeting will further highlight changes in steroid usage patterns and outcomes following treatment initiation with Ultomiris or Soliris. Results from the open-label extension of the pivotal, global Phase III CHAMPION-MG trial evaluating the safety and efficacy of Ultomiris in adults with AChR Ab+ gMG will show decreased steroid use in Ultomiris-treated patients. Additionally, a retrospective cohort study from a United States (US) claims database will highlight that Ultomiris and Soliris facilitated significant steroid sparing within the first year of their initiation.

Real-world data underscoring the safety and efficacy of Ultomiris and Soliris in clinical practice

New real-world data from a retrospective medical record analysis will be presented at the MGFA Scientific Session, reporting outcomes among gMG patients in the US treated with Ultomiris, Soliris and Vyvgart. Although patient characteristics differed between the treatment groups, results will suggest that Ultomiris may provide greater symptom control than alternative therapies as measured by MG Activities of Daily Living (MG-ADL) scores.

At the AANEM Annual Meeting, two encore presentations of results from a global gMG registry will suggest Ultomiris and Soliris may improve activities of daily living and quality of life in adults with AChR Ab+ gMG. In an interim analysis, patients initiating Ultomiris showed improvements in MG-ADL, including achieving minimal symptom expression, and MG Foundation of America Clinical Class (MGFA-CC) scores. Further, sustained improvements were observed when transitioning from Soliris to Ultomiris. Additionally, an analysis of Myasthenia Gravis Quality of Life15-revised (MG-QOL15r) scores will show clinically meaningful improvement in patients who initiated treatment with Ultomiris and Soliris, with further improvements observed among patients transitioning from Soliris to Ultomiris.

Further, safety outcomes in pregnant patients treated with Soliris across all approved indications will be reported at the MGFA Scientific Session. This cumulative analysis from the Alexion pharmacovigilance safety database offers valuable insights for patients and for clinical decision-making.

Advancing understanding and care for the gMG community

At the MGFA Scientific Session, a poster presentation will offer insight into indirect and non-medical costs of gMG, as reported by US patients and caregivers via a web-based survey. Results will show high annual indirect and nonmedical costs for both patients and caregivers, including lost work and social productivity, contributing substantially to the total economic impact of gMG.

Another poster presentation will provide an overview of the ongoing pivotal, global Phase III PREVAIL trial evaluating the efficacy and safety of gefurulimab, an investigational C5 inhibitor optimised for weekly subcutaneous administration, in adults with AChR Ab+ gMG.

Alexion presentations during the 2024 AANEM Annual Meeting and MGFA Scientific Session

Lead Author  Abstract Title  Presentation Details 
Nicolle, M Concomitant AANEM Annual MeetingPoster Presentation 236
corticosteroid 16 October 202418:15-18:4517 October
use in 202414:45-15:15
ravulizumab
-treated adults
with anti
-acetylcholine
receptor antibody
-positive
generalized
myasthenia
gravis: final
results from the
phase 3 CHAMPION
-MG Open-label
Extension
(Encore)
Blackowicz, M Long-term AANEM Annual MeetingPoster Presentation 145
corticosteroid 16 October 202418:15-18:4517 October
treatments 202414:45-15:15
patterns and
steroid-sparing
effects of
approved
treatments for
generalized
myasthenia gravis
in the United
States (Encore)
Narayanaswami, Safety and AANEM Annual MeetingPoster Presentation 234
P effectiveness of 16 October 202418:15-18:4517 October
ravulizumab in 202414:45-15:15
generalized
myasthenia
gravis: evidence
from a global
registry (Encore)
Scheiner, C Quality of life AANEM Annual MeetingPoster Presentation 267
in generalized 16 October 202418:15-18:45 17 October
myasthenia 20249:30-10:00
gravis: results
from a global
registry of
eculizumab and
ravulizumab
treatment
(Encore)
Yee, K Patient AANEM Annual MeetingPoster Presentation
preferences for 31016 October 202418:15-18:45 17 October
generalized 202414:45-15:15
myasthenia gravis
treatment
profiles: results
of a web-based
survey (Encore)
Pandya, S Incidence and AANEM Annual MeetingPoster Presentation 240
outcome of 16 October 202418:15-18:4517 October
meningococcal 202414:45-15:15MGFA Scientific
infection with SessionPoster Presentation MG55 15 October
eculizumab or 202412:00-12:45
ravulizumab in
patients with gMG
or NMOSD: An
analysis of US
clinical practice
(Encore) 
Nowak, R Change in MGFA Scientific SessionPoster Presentation
concomitant MG8615 October 202412:00-12:45
immunosuppressive
therapies for
generalized
myasthenia gravis
in patients
receiving
complement C5
inhibitor
therapies: a
retrospective
analysis of
registry data
Scheiner, C Outcomes for MGFA Scientific SessionPoster Presentation
patients with MG8515 October 202412:00-12:45
generalized
myasthenia gravis
prescribed
ravulizumab,
eculizumab, or
efgartigimod
treatment:
interim analysis
of a
retrospective
medical record
analysis
(ELEVATE)
Narayanaswami, Safety outcomes MGFA Scientific SessionPoster Presentation
P in pregnant MG10115 October 202412:00-12:45
patients treated
with the
complement 5
inhibitor therapy
(C5IT)
eculizumab 
Howard, J The phase 3 MGFA Scientific SessionPoster Presentation
PREVAIL study MG9915 October 202412:00-12:45
assessing the
efficacy and
safety of
subcutaneous
gefurulimab in
adults with
generalized
myasthenia
gravis: trial in
progress 
Gwathmey, K Evaluation of the MGFA Scientific SessionPoster Presentation
indirect and MG9815 October 202412:00-12:45
nonmedical
impacts of
generalized
myasthenia gravis
on patients and
caregivers 

Notes

Alexion

Alexion, AstraZeneca Rare Disease is focused on serving patients and families affected by rare diseases and devastating conditions through the discovery, development and delivery of life-changing medicines. A pioneering leader in rare disease for more than three decades, Alexion was the first to translate the complex biology of the complement system into transformative medicines, and today it continues to build a diversified pipeline across disease areas with significant unmet need, using an array of innovative modalities. As part of AstraZeneca, Alexion is continually expanding its global geographic footprint to serve more rare disease patients around the world. It is headquartered in Boston, US.  

AstraZeneca

AstraZeneca (LSE/STO/Nasdaq: AZN) is a global, science-led biopharmaceutical company that focuses on the discovery, development, and commercialisation of prescription medicines in Oncology, Rare Diseases, and BioPharmaceuticals, including Cardiovascular, Renal & Metabolism, and Respiratory & Immunology. Based in Cambridge, UK, AstraZeneca's innovative medicines are sold in over 125 countries and used by millions of patients worldwide. Please visit astrazeneca.com (http://www.astrazeneca.com/) and follow the Company on social media @AstraZeneca (https://www.linkedin.com/company/astrazeneca/mycompany/verification/).

Contacts

For details on how to contact the Investor Relations Team, please click here (https://www.astrazeneca.com/investor-relations.html#Contacts). For Media contacts, click here (https://www.astrazeneca.com/media-centre/contacts.html).