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AstraZeneca receives final regulatory clearance for the proposed acquisition of Alexion from the UK’s Competition and Markets Authority

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NOT FOR RELEASE, PUBLICATION OR DISTRIBUTION, IN WHOLE OR IN PART, DIRECTLY OR INDIRECTLY, IN OR INTO OR FROM ANY JURISDICTION WHERE TO DO SO WOULD CONSTITUTE A VIOLATION OF THE RELEVANT LAWS OR REGULATIONS OF SUCH JURISDICTION.

THIS IS AN ANNOUNCEMENT AND NOT A CIRCULAR OR PROSPECTUS OR EQUIVALENT DOCUMENT FOR THE PURPOSES OF THE UK PROSPECTUS REGULATION RULES OR THE UK AND EU PROSPECTUS REGULATIONS. THIS ANNOUNCEMENT DOES NOT CONSTITUTE OR FORM PART OF, AND SHOULD NOT BE CONSTRUED AS, ANY OFFER, INVITATION OR RECOMMENDATION TO PURCHASE, SELL OR SUBSCRIBE FOR ANY SECURITIES IN ANY JURISDICTION AND NEITHER THE ISSUE OF THE INFORMATION NOR ANYTHING CONTAINED HEREIN SHALL FORM THE BASIS OF OR BE RELIED UPON IN CONNECTION WITH, OR ACT AS AN INDUCEMENT TO ENTER INTO, ANY INVESTMENT ACTIVITY. INVESTORS AND PROSPECTIVE INVESTORS SHOULD NOT MAKE ANY INVESTMENT DECISION ON THE BASIS OF ITS CONTENTS.

The UK Competition and Markets Authority has cleared AstraZeneca’s proposed acquisition of Alexion Pharmaceuticals, Inc. (Alexion). As a result, the acquisition is expected to close on 21 July 2021.

Following closing, the new AstraZeneca shares issued to Alexion shareholders will be admitted to listing on the premium listing segment of the official list of the UK Financial Conduct Authority (FCA) and to the secondary listing on Nasdaq Stockholm. In addition, the new AstraZeneca American Depositary Shares (ADSs) will be admitted on the Nasdaq Stock Market. Trading on the London Stock Exchange’s main market for listed securities, Nasdaq Stockholm and the Nasdaq Stock Market, is expected to commence on 22 July 2021. In addition, the Alexion shares will be de‐listed from the Nasdaq Stock Market. They will be deregistered under the Exchange Act as soon as practicable following completion of the acquisition.

Marc Dunoyer, Executive Director and Chief Financial Officer, said: “We are very pleased to have secured this critical final clearance from the UK Competition and Markets Authority for the acquisition of Alexion. We look forward to the imminent closing of the transaction so that we may pursue our shared ambition to bring more innovative medicines to patients worldwide and begin AstraZeneca’s next chapter of growth.”

The proposed acquisition, first announced in December 2020, will enhance the Company’s scientific presence in immunology by adding Alexion’s innovative complement-technology platforms and robust pipeline. Rare diseases represent a high-growth opportunity with rapid innovation and significant unmet medical needs. Shareholders of both companies overwhelmingly voted in support of the transaction on 11 May 2021.

Subject to completing the acquisition, a group focusing on rare diseases will be created. This group will be named ‘Alexion, AstraZeneca Rare Disease’, and will be headquartered in Boston, US.

Financial considerations

AstraZeneca anticipates providing updated 2021 financial guidance for the new, combined entity in due course. Consolidation of Alexion will start from the closing of the transaction and the first quarter of consolidated financial reporting is expected to be the third quarter of 2021 due for announcement on Wednesday 10 November 2021.

Rare diseases

Over 7,000 rare diseases are known today, and only approximately 5% have treatments approved by the US Food and Drug Administration.1 Demand in medicines for rare diseases is forecasted to grow by a low double-digit percentage in the future.2

Important additional information

In connection with AstraZeneca’s proposed acquisition of Alexion (the Acquisition), AstraZeneca filed a registration statement on Form F-4 with the SEC on 12 April 2021 (the Registration Statement), which has been declared effective by the United States Securities and Exchange Commission, and which includes a document that serves as a prospectus of AstraZeneca and a proxy statement of Alexion (the proxy statement/prospectus), Alexion filed a proxy statement with the SEC (the proxy statement) on 12 April 2021, and each party will file other documents regarding the Acquisition with the SEC. Investors and security holders of Alexion are urged to carefully read the entire Registration Statement and proxy statement/prospectus or proxy statement and other relevant documents filed with the SEC when they become available, because they will contain important information. Investors and security holders may obtain the Registration Statement and the proxy statement/prospectus or the proxy statement free of charge from the SEC’s website or from AstraZeneca or Alexion as described in the paragraphs below.

The documents filed by AstraZeneca with the SEC may be obtained free of charge at the SEC’s website at www.sec.gov. These documents may also be obtained free of charge on AstraZeneca’s website at https://www.astrazeneca.com under the tab “Investors”. The documents filed by Alexion with the SEC may be obtained free of charge at the SEC’s website at www.sec.gov. These documents may also be obtained free of charge on Alexion’s internet website at https://www.alexion.com under the tab, “Investors” and under the heading “SEC Filings” or by contacting Alexion’s Investor Relations Department at investorrelations@alexion.com.

Important notices relating to financial advisors

Evercore Partners International LLP (Evercore), which is authorised and regulated by the FCA in the United Kingdom, is acting exclusively for AstraZeneca and no one else in connection with the Acquisition and the matters referred to in this announcement and will not regard any other person as a client in relation to the matters set out in this announcement (whether or not a recipient of this announcement) and will not be responsible to anyone other than AstraZeneca for providing the protections afforded to its clients, nor for providing advice in relation to the Acquisition or any other matter referred to in this announcement. Neither Evercore nor any of its subsidiaries, holding companies, branches or affiliates owes or accepts any duty, liability or responsibility whatsoever (whether direct or indirect, whether in contract, in tort, under statute or otherwise) to any person who is not a client in connection with the Acquisition or any statement contained in this announcement or otherwise. Apart from the responsibilities and liabilities, if any, which may be imposed on Evercore by the Financial Services and Markets Act 2000 (FSMA), or the regulatory regime established thereunder, or under the regulatory regime of any jurisdiction where exclusion of liability under the relevant regulatory regime would be illegal, void or unenforceable, neither Evercore nor any of its affiliates accepts any responsibility or liability whatsoever for the contents of this announcement, and no representation, express or implied, is made by it, or purported to be made on its behalf, in relation to the contents of this announcement, including their accuracy, fairness, sufficiency, completeness or verification of any statement contained in this announcement or any other statement made or purported to be made by it, or on its behalf, in connection with AstraZeneca or the matters described in announcement, and nothing in this announcement is, or shall be relied upon as, a promise or representation in this respect, whether as to the past or the future. To the fullest extent permitted by applicable law, each of Evercore and its affiliates accordingly disclaim all and any responsibility or liability whether arising in tort, contract or otherwise (save as referred to above) which they might otherwise have in respect of this announcement, or any statement contained in this announcement.

Centerview Partners UK LLP (Centerview Partners), which is authorised and regulated by the FCA in the United Kingdom, is acting exclusively for AstraZeneca and no one else in connection with the Acquisition and the matters referred to in this announcement and will not regard any other person as a client in relation to the matters set out in this announcement (whether or not a recipient of this announcement) and will not be responsible to anyone other than AstraZeneca for providing the protections afforded to its clients, nor for providing advice in relation to the Acquisition or any other matter referred to in this announcement. Neither Centerview Partners nor any of its subsidiaries, holding companies, branches or affiliates owes or accepts any duty, liability or responsibility whatsoever (whether direct or indirect, whether in contract, in tort, under statute or otherwise) to any person who is not a client in connection with the Acquisition or any statement contained in this announcement or otherwise. Apart from the responsibilities and liabilities, if any, which may be imposed on Centerview Partners by the FSMA, or the regulatory regime established thereunder, or under the regulatory regime of any jurisdiction where exclusion of liability under the relevant regulatory regime would be illegal, void or unenforceable, neither Centerview Partners nor any of its affiliates accepts any responsibility or liability whatsoever for the contents of this announcement, and no representation, express or implied, is made by it, or purported to be made on its behalf, in relation to the contents of this announcement, including their accuracy, fairness, sufficiency, completeness or verification of any statement contained in this announcement or any other statement made or purported to be made by it, or on its behalf, in connection with AstraZeneca or the matters described in this announcement, and nothing in this announcement is, or shall be relied upon as, a promise or representation in this respect, whether as to the past or the future. To the fullest extent permitted by applicable law, each of Centerview Partners and its affiliates accordingly disclaim all and any responsibility or liability whether arising in tort, contract or otherwise (save as referred to above) which they might otherwise have in respect of this announcement, or any statement contained in this announcement.

Forward-looking statements

This announcement contains certain forward-looking statements with respect to the operations, performance and financial condition of the AstraZeneca Group, including, among other things, statements about expected revenues, margins, earnings per share or other financial or other measures, as well as the ability of the parties to consummate the Acquisition on a timely basis or at all, the ability of the parties to satisfy the conditions precedent to consummation of the Acquisition, including the ability to secure the required regulatory approvals on the terms expected, at all or in a timely manner, the ability of AstraZeneca to successfully integrate Alexion’s operations, and the ability of AstraZeneca to implement its plans, forecasts and other expectations with respect to Alexion’s business after Completion and realise expected synergies. Although the AstraZeneca Group believes its expectations are based on reasonable assumptions, any forward-looking statements, by their very nature, involve risks and uncertainties and may be influenced by factors that could cause actual outcomes and results to be materially different from those predicted. The forward-looking statements reflect knowledge and information available at the date of preparation of this announcement and the AstraZeneca Group undertakes no obligation to update these forward-looking statements. The AstraZeneca Group identifies the forward-looking statements by using the words ‘anticipates’, ‘believes’, ‘expects’, ‘intends’ and similar expressions in such statements. Important factors that could cause actual results to differ materially from those contained in forward-looking statements, certain of which are beyond the AstraZeneca Group’s control, include, among other things: the risks set out in Part II (Risk Factors) of the AstraZeneca shareholder circular published on 12 April 2021; failure or delay in delivery of pipeline or launch of new medicines; failure to meet regulatory or ethical requirements for medicine development or approval; failure to obtain, defend and enforce effective intellectual property (IP) protection and IP challenges by third parties; competitive pressures including expiry or loss of IP rights, and generic competition; price controls and reductions; economic, regulatory and political pressures; uncertainty and volatility in relation to the UK’s exit from the EU; failures or delays in the quality or execution of commercial strategies; failure to maintain supply of compliant, quality medicines; illegal trade in medicines; reliance on third-party goods and services; failure in information technology, data protection or cybercrime; failure of critical processes; uncertainty of expected gains from productivity initiatives; failure to attract, develop, engage and retain a diverse, talented and capable workforce, including following Completion; failure to adhere to applicable laws, rules and regulations; the safety and efficacy of marketed medicines being questioned; adverse outcome of litigation and/or governmental investigations, including relating to the Acquisition; failure to adhere to increasingly stringent anti-bribery and anti-corruption legislation; failure to achieve strategic plans or meet targets or expectations; failure in financial control or the occurrence of fraud; unexpected deterioration in AstraZeneca’s or Alexion’s financial position; the impact that the COVID-19 global pandemic may have or continue to have on these risks, on AstraZeneca’s ability to continue to mitigate these risks, and on AstraZeneca’s operations, financial results or financial condition; the risk that a condition to the closing of the Acquisition may not be satisfied, or that a regulatory approval that may be required for the Acquisition is delayed or is obtained subject to conditions that are not anticipated; the risk that AstraZeneca is unable to achieve the synergies and value creation contemplated by the Acquisition, or that AstraZeneca is unable to promptly and effectively integrate Alexion’s businesses; and the risk that management’s time and attention are diverted on Acquisition-related issues or that disruption from the Acquisition makes it more difficult to maintain business, contractual and operational relationships.

Neither AstraZeneca nor any of its associates or directors, officers or advisers provides any representation, assurance or guarantee that the occurrence of the events expressed or implied in any forward-looking statements in this announcement will actually occur. You are cautioned not to place undue reliance on these forward-looking statements. Other than in accordance with their legal or regulatory obligations (including under the Listing Rules, the Disclosure and Transparency Rules and the Prospectus Regulation Rules of the FCA), AstraZeneca is under no obligation, and AstraZeneca expressly disclaims any intention or obligation to update or revise publicly any forward-looking statements, whether as a result of new information, future events or otherwise.

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 and BioPharmaceuticals, including Cardiovascular, Renal & Metabolism, and Respiratory & Immunology. Based in Cambridge, UK, AstraZeneca operates in over 100 countries, and its innovative medicines are used by millions of patients worldwide. Please visit astrazeneca.com and follow the Company on Twitter @AstraZeneca.

Contacts

For details on how to contact the Investor Relations Team, please click here. For Media contacts, click here.

References

1. In the US, a rare disease impacts less than 200,000 patients (as defined in the US Orphan Drug Act 1983).

2. EvaluatePharma, World Preview 2020, Outlook to 2026.

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Holmens styrelse har beslutat om återköp av aktier kopplat till aktiesparprogram

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Styrelsen för Holmen har beslutat att utnyttja bemyndigandet från årsstämman den 16 april 2024 om återköp av egna aktier för framtida leverans av aktier till deltagare i Holmens långsiktiga aktiesparprogram.

Återköp får omfatta högst 50 000 aktier av serie B under perioden från och med 29 april 2024 fram till och med den 31 maj 2024, vid ett eller flera tillfällen. Återköp ska ske på Nasdaq Stockholm i enlighet med dess Regelverk för emittenter till ett pris per aktie inom det på Nasdaq Stockholm vid var tid gällande kursintervallet mellan högsta köpkurs och lägsta säljkurs.

Syftet med återköpet är att säkerställa framtida leverans av aktier till deltagare i Holmens långsiktiga aktiesparprogram.

Holmen innehar vid tidpunkten för detta pressmeddelande 3 289 969 egna aktier av serie B, motsvarande 2 % av totalt antal aktier.

För ytterligare information, vänligen kontakta:
Stina Sandell, Hållbarhets- och kommunikationsdirektör, Holmen, 073 986 51 12

Holmens verksamhet utgår från skogens kretslopp och de förnybara produkter vi kan skapa av det. Vi är 3 500 medarbetare som skapar värde för aktieägare, kunder och samhälle. Vår omsättning uppgick 2023 till nästan 23 Mdkr och aktien är noterad på Nasdaq Stockholm, Large Cap. Välkommen att besöka holmen.com för mer information.

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DexTech Medical AB, Delårsrapport 1 juli, 2023 – 31 mars 2024

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Sammanfattning av tredje kvartalet (2024-01-01 – 2024-03-31)

  • Nettoomsättningen uppgick till 0,0 (0,0) MSEK
  • Rörelseresultatet uppgick till -1,5 (-1,6) MSEK
  • Resultat per aktie* -0,08 (-0,08) SEK

Sammanfattning av niomånadersperioden (2023-07-01 – 2024-03-31)

  • Nettoomsättningen uppgick till 0,0 (0,0) MSEK
  • Rörelseresultatet uppgick till -3,9 (-3,7) MSEK
  • Resultat per aktie* -0,18 (-0,19) SEK
  • Likvida medel uppgick vid periodens utgång till 21,1 (27,1) MSEK

* Före och efter utspädning. Resultat per aktie: Periodens resultat dividerat med genomsnittligt antal aktier 18 485 857. För jämförelseperioden var genomsnittligt antal aktier 18 485 857. Belopp inom parentes avser motsvarande period föregående år.

VD:s kommentar 

Bolagets fas1 studie avseende OsteoDex behandling av multipelt myelom pågår och patientrekryteringen fortskrider.

 Huvudprövare (principal investigator, PI) är Dr Katarina Uttervall, MD, PhD, Avdelningen för Hematologi/HERM, Karolinska Universitetssjukhuset, Huddinge. Biomarkörer analyseras vid Centrallaboratoriet, Karolinska Universitetssjukhuset, NKS, Solna. Patienter med recidiverande/behandlingsresistent sjukdom och som erhållit 1–5 tidigare behandlingslinjer inkluderas. Primär målsättning är att konfirmera säkerhet och tolererbarhet samt som sekundär målsättning att fastställa eventuell behandlingsrespons. Dokumentering av livskvalité́ kommer även att göras (QoL scores).

Den första patienten behandlades i december vid Karolinska Universitetssjukhuset i Huddinge. De första provsvaren från patient 1 inkom den 23 januari och visar en mycket stark effekt på markören för osteoklast aktivitet (CTX).  Patienten har nu fullgjort behandlingen enligt studieprotokollet och har nu stabil sjukdom. Stabil sjukdom innebär att sjukdomen ej fortskrider (bromsad). Resultatet är viktigt och indikerar att Osteodex kan bromsa recidiverande/behandlingsresistent sjukdom.

Ett amendment till studieprotokollet som innebär att Bolaget kan följa patientens sjukdomshistoria efter fullgjord behandling är nu godkänt av berörda myndigheter. Det ger Bolaget information om durationen av OsteoDex sjukdomsbromasande effekt.

Anders R Holmberg

Kontaktpersoner

Anders Holmberg, verkställande direktör, +46 73 324 27 82

Gösta Lundgren, CFO, +46 70 710 47 88

Denna information är sådan information som DexTech Medical AB är skyldigt att offentliggöra enligt EU:s marknadsmissbruksförordning. Informationen lämnades, genom ovanstående kontaktpersoners försorg, för offentliggörande den 26 april 2024.

DexTech Medical AB är ett svenskt forskningsföretag som utifrån sin teknikplattform har utvecklat fyra läkemedelskandidater som skyddas av patent. Huvudkandidaten är OsteoDex för behandling av kastrationsresistent prostatacancer (CRPC) med skelettmetastaser. En framgångsrik klinisk fas II studie har genomförts med OsteoDex där resultatet visar hög tolererbarhet med lindriga biverkningar samt behandlingseffekt på patienter som sviktar på befintliga läkemedel. DexTechs målsättning är att senast efter genomförd fas II-studie utlicensiera respektive läkemedelskandidat. DexTech Medical AB är noterat på Spotlight Stock Market.

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Paulina Brandberg besöker Falun

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Måndagen den 29 april besöker jämställdhets- och biträdande arbetsmarknadsminister Paulina Brandberg Falun. Hon kommer bland annat att delta i möte med landshövding Helena Höij kring arbetet mot mäns våld mot kvinnor, annat våld i nära relationer och hedersrelaterat våld och förtryck och göra ett verksamhetsbesök vid Polisen i Dalarna. 

Vid mötet med landshövdingen kommer Paulina Brandberg att få information om ”Ett Dalarna fritt från våld”, Dalarnas jämställdhetsstrategi samt en lägesrapport kring länets regionala resurscentrum mot hedersrelaterat våld och förtryck. Vid mötet deltar landshövdingen, representanter från Länsstyrelsen, Polisen och Region Dalarna. 

Paulina Brandberg kommer också att göra ett verksamhetsbesök vid Polisen för att få en fördjupad inblick i deras arbete mot våldet.

Program 

12.00-14.00 Möte med landshövdingen

14.00-14.30 Tid för media
Adress ges vid anmälan.

14.30-16.30 Verksamhetsbesök Polisen 

16.30-17.00 Tid för media
Adress ges vid anmälan.

Kontakta Emelie Franzén vid intervjuförfrågningar.
 

Kontakt
Emelie Franzén
Pressassistent hos jämställdhets- och biträdande arbetsmarknadsminister Paulina Brandberg
076-771 09 51
emelie.franzen@regeringskansliet.se

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