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Imfinzi approved in China for the treatment of extensive-stage small cell lung cancer

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Only PD-1/PD-L1 immunotherapy to demonstrate both a significant survival benefit and improved response rate in combination with a choice of chemotherapies 

AstraZeneca’s Imfinzi (durvalumab) has been approved in China for the 1st-line treatment of adult patients with extensive-stage small cell lung cancer (ES-SCLC), in combination with standard of care platinum chemotherapy (etoposide plus a choice of either carboplatin or cisplatin).

The approval by China’s National Medical Products Administration was based on positive results from the CASPIAN Phase III trial. The trial showed that Imfinzi plus chemotherapy demonstrated a statistically significant and clinically meaningful improvement in overall survival (OS) versus chemotherapy alone. In addition, results from the China cohort of patients were consistent with the global results.

Small cell lung cancer (SCLC) is a highly aggressive, fast-growing form of lung cancer that typically recurs and progresses rapidly despite initial response to chemotherapy.1,2 Prognosis is particularly poor, as only 7% of all SCLC patients and 3% of those with extensive-stage disease will be alive five years after diagnosis.3

Dave Fredrickson, Executive Vice President, Oncology Business Unit, said: “Today’s approval of Imfinzi plus chemotherapy brings an important global standard of care to patients with extensive-stage small cell lung cancer in China, who have had few treatment options and a dire prognosis. Physicians can now offer these patients a well-tolerated immunotherapy regimen with sustained overall survival and prolonged treatment response, as well as convenient dosing. This is also the first time physicians have had the choice to combine immunotherapy with cisplatin, a preferred chemotherapy in this setting in China.”

The CASPIAN Phase III trial met the primary endpoint of OS for Imfinzi plus chemotherapy in June 2019, reducing the risk of death by 27% versus chemotherapy alone (based on a hazard ratio [HR] of 0.73; 95% confidence interval [CI] 0.59-0.91; p=0.0047), with a median OS of 13.0 months versus 10.3 months for chemotherapy alone. These results were published in The Lancet in October 2019.4 Results also showed an increased confirmed objective response rate for Imfinzi plus chemotherapy (68% versus 58% for chemotherapy alone). Imfinzi added to chemotherapy delayed the time for disease symptoms to worsen.4

An updated analysis showed sustained efficacy for Imfinzi plus chemotherapy after a median follow up of more than two years (OS HR of 0.75; 95% CI 0.62-0.91; nominal p=0.0032), with median OS of 12.9 months versus 10.5 months for chemotherapy alone. An estimated 22.2% of patients treated with Imfinzi plus chemotherapy were alive at 24 months versus 14.4% for chemotherapy alone. The safety and tolerability for Imfinzi and chemotherapy were consistent with the known safety profiles of these medicines. No patients tested positive for treatment-emergent anti-drug antibodies to Imfinzi.

Safety and efficacy results in the China cohort of patients were consistent with results in the overall global trial population. Detailed results from this cohort will be presented at a forthcoming medical meeting.

The CASPIAN Phase III trial used a fixed dose of Imfinzi (1500mg) administered every three weeks for four cycles while in combination with chemotherapy and then every four weeks as a monotherapy until disease progression. Based on the trial results, Imfinzi, in combination with etoposide and either carboplatin or cisplatin, is approved in the 1st-line setting of ES-SCLC in more than 55 countries, including the US, Japan and across the EU.

Imfinzi is also being tested following concurrent chemoradiation therapy in patients with limited-stage SCLC in the ADRIATIC Phase III trial as part of a broad development programme. In addition, Imfinzi is also approved to treat non-small cell lung cancer (NSCLC) in the curative-intent setting of unresectable, Stage III disease after chemoradiation therapy in the US, Japan, China, across the EU and in many other countries, based on results from the PACIFIC Phase III trial.

Small cell lung cancer

Lung cancer is the leading cause of cancer death among men and women and accounts for about one-fifth of all cancer deaths.5 Lung cancer is broadly split into NSCLC and SCLC, with about 15% classified as SCLC.6 About two-thirds of SCLC patients are diagnosed with extensive-stage disease, in which the cancer has spread widely through the lung or to other parts of the body.3

CASPIAN

CASPIAN was a randomised, open-label, multi-centre, global Phase III trial in the 1st-line treatment of 805 patients with ES-SCLC. The trial compared Imfinzi in combination with etoposide and either carboplatin or cisplatin platinum chemotherapy, or Imfinzi and chemotherapy with the addition of a second immunotherapy, tremelimumab, versus chemotherapy alone. In the two experimental arms, patients were treated with four cycles of chemotherapy. In comparison, the control arm allowed up to six cycles of chemotherapy and optional prophylactic cranial irradiation.

The trial was conducted in more than 200 centres across 23 countries, including the US, Europe, South America, Asia and the Middle East. The primary endpoint was OS in each of the two experimental arms. In June 2019, AstraZeneca announced the CASPIAN Phase III trial had met one primary endpoint of demonstrating OS for Imfinzi plus chemotherapy at a planned interim analysis. In March 2020, however, it was announced that the second experimental arm with tremelimumab did not meet its primary endpoint of OS.

Imfinzi

Imfinzi (durvalumab) is a human monoclonal antibody that binds to PD-L1 and blocks the interaction of PD-L1 with PD-1 and CD80, countering the tumour’s immune-evading tactics and releasing the inhibition of immune responses.

In addition to approvals in ES-SCLC and unresectable, Stage III NSCLC, Imfinzi is approved for previously treated patients with advanced bladder cancer in several countries. Since the first approval in May 2017, more than 100,000 patients have been treated with Imfinzi.

As part of a broad development programme, Imfinzi is being tested as a single treatment and in combinations with other anti-cancer treatments for patients with NSCLC, SCLC, bladder cancer, hepatocellular carcinoma, biliary tract cancer (a form of liver cancer), oesophageal cancer, gastric and gastroesophageal cancer, cervical cancer, ovarian cancer, endometrial cancer, and other solid tumours.

AstraZeneca in lung cancer

AstraZeneca is working to bring patients with lung cancer closer to cure through the detection and treatment of early-stage disease, while also pushing the boundaries of science to improve outcomes in the resistant and advanced settings. By defining new therapeutic targets and investigating innovative approaches, the Company aims to match medicines to the patients who can benefit most.

The Company’s comprehensive portfolio includes leading lung cancer medicines and the next wave of innovations, including Tagrisso (osimertinib) and Iressa (gefitinib); Imfinzi (durvalumab) and tremelimumab; Enhertu (trastuzumab deruxtecan) and datopotamab deruxtecan in collaboration with Daiichi Sankyo; Orpathys (savolitinib) in collaboration with HUTCHMED; as well as a pipeline of potential new medicines and combinations across diverse mechanisms of action.

AstraZeneca is a founding member of the Lung Ambition Alliance, a global coalition working to accelerate innovation and deliver meaningful improvements for people with lung cancer, including and beyond treatment.

AstraZeneca in immunotherapy

Immunotherapy is a therapeutic approach designed to stimulate the body’s immune system to attack tumours. The Company’s IO portfolio is anchored in immunotherapies that have been designed to overcome anti-tumour immune suppression. AstraZeneca is invested in using IO approaches that deliver long-term survival for new groups of patients across tumour types.

The Company is pursuing a comprehensive clinical-trial programme that includes Imfinzi as a single treatment and in combination with tremelimumab and other novel antibodies in multiple tumour types, stages of disease, and lines of treatment, and where relevant using the PD-L1 biomarker as a decision-making tool to define the best potential treatment path for a patient. In addition, the ability to combine the IO portfolio with radiation, chemotherapy, small, targeted molecules from across AstraZeneca’s oncology pipeline, and from research partners, may provide new treatment options across a broad range of tumours.

AstraZeneca in oncology

AstraZeneca is leading a revolution in oncology with the ambition to provide cures for cancer in every form, following the science to understand cancer and all its complexities to discover, develop and deliver life-changing medicines to patients.

The Company’s focus is on some of the most challenging cancers. It is through persistent innovation that AstraZeneca has built one of the most diverse portfolios and pipelines in the industry, with the potential to catalyse changes in the practice of medicine and transform the patient experience.

AstraZeneca has the vision to redefine cancer care and, one day, eliminate cancer as a cause of death.

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

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References

  1. National Cancer Institute. NCI Dictionary – Small Cell Lung Cancer. Available at https://www.cancer.gov/publications/dictionaries/cancer-terms/def/small-cell-lung-cancer. Accessed July 2021.
  2. Kalemkerian GP, et al. Treatment Options for Relapsed Small-Cell Lung Cancer: What Progress Have We Made? J Oncol Pract, 2018:14;369-370.
  3. Cancer.Net. Lung Cancer – Small Cell. Available at https://www.cancer.net/cancer-types/33776/view-all. Accessed July 2021.
  4. Paz-Ares L, et al. Durvalumab plus platinum-etoposide versus platinum-etoposide in first-line treatment of extensive-stage small cell lung cancer (CASPIAN): a randomised, controlled, open-label, Phase III trial. The Lancet. 2019;394(10212):1929-1939.
  5. World Health Organization. International Agency for Research on Cancer. Lung Fact Sheet. Available at https://gco.iarc.fr/today/data/factsheets/cancers/15-Lung-fact-sheet.pdf. Accessed July 2021.
  6. LUNGevity Foundation. Types of Lung Cancer. Available at https://lungevity.org/for-patients-caregivers/lung-cancer-101/types-of-lung-cancer. Accessed July 2021.
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Naomi Klein till Stockholm 16 maj

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För första gången sedan 2015 kommer författaren och aktivisten Naomi Klein till Sverige. Den 16 maj kl 19.30 berättar hon om sin nya bok på Rival i Stockholm. Kvällen är ett samarbete mellan Ordfront förlag, Katalys, Antropocenlaboratoriet, Aftonbladet kultur och ABF Stockholm.

NaomiKleincreditSebastianNevols

Författaren, journalisten och aktivisten Naomi Klein är en av vår tids största tänkare. Hon är känd för sina banbrytande böcker om globalisering, kapitalism och klimatförändringar såsom No logo, Chockdoktrinen och Det här förändrar allt.

Nu kommer hon för första gången på nästan tio år till Sverige, Stockholm, för att tala om sin senaste bok.

Boken, Doppelgänger – En färd genom spegelvärlden, är en slags guidebok för en illavarslande samtid, för alla som har gått vilse i internets irrgångar och undrar varför politiken har blivit så galet snedvriden. På största allvar konfronterar Naomi Klein konspirationstänkandets dubbelexponeringar och tar till sin hjälp bland annat Sigmund Freud, Jordan Peele, Alfred Hitchcock och bell hooks. Klein analyserar skickligt samtidens förvridna nyhetsrapportering och politiska klimat, och med humor och värme ger hon oss en berättelse som går närmare inpå det egna jaget än någonsin förr. Finns det en väg ut ur denna kollektiva yrsel och hur kan vi kämpa för det som verkligen betyder något?

Den 16 maj kl 19.30 samtalar Naomi Klein med Aftonbladets kulturchef Karin Pettersson på Rival i Stockholm. Missa inte denna unika chans att höra Naomi Klein live. Kvällen är ett samarbete mellan Ordfront förlag, Katalys, Antropocenlaboratoriet, Aftonbladet kultur och ABF Stockholm. 

Här kan du köpa biljetter.

För pressförfrågningar kontakta: Christoph Fielder, christoph@ordfrontforlag.se eller Jenny Bjarnar, jenny@ordfrontforlag.se

Läs mer om Naomi Klein här samt ladda ner pressbilder.

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Kommuniké från extra bolagsstämma i AegirBio AB (publ) den 26 april 2024

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AegirBio AB (publ) höll den 26 april 2024 extra bolagsstämma. Stämman fattade i huvudsak följande beslut.

Val av styrelse

Stämman beslutade att styrelsen ska bestå av sex (6) styrelseledamöter utan suppleanter för tiden intill slutet av årsstämman 2024.

Stämman beslutade att omvälja Marco Witteveen, Fredrik Häglund och William Vickery samt att välja Bill Ferenczy, Jens Umehag och Michael Schwartz till nya styrelseledamöter, samtliga för tiden intill årsstämman 2024, samt att Anders Ingvarsson inte längre ska kvarstå i styrelsen. Stämman beslutade att välja Jens Umehag som styrelsens ordförande.

Beslut om ändring av villkor för konvertibler av serie 2023/2025

Stämman beslutade, i enlighet med styrelsens förslag, om ändring av villkoren för bolagets konvertibler av serie 2023/2025 som beslutades på extra bolagsstämma den 20 januari 2023. De huvudsakliga ändringarna innebär att:

1. lånets förfallodag ändras till den 20 januari 2026

2. konvertering kan påkallas till och med den 2 januari 2026

3. ingen begäran för konvertering ska vara för mindre än 500 000.

För mer detaljerad information om innehållet i beslutet hänvisas till den fullständiga kallelsen till extra bolagsstämman.

Kallelse till extra bolagsstämman samt fullständigt förslag avseende extra bolagsstämmans beslut finns tillgängligt på bolagets hemsida, www.aegirbio.com.

För ytterligare information, vänligen kontakta:

Christel Dahlberg, CFO Aegirbio AB

Epost: ir@aegirbio.com

AegirBio i korthet

AegirBio är ett svenskt diagnostikföretag som grundades 2019 för att erbjuda tester för att övervaka och optimera doseringen av biologiska läkemedel via sin unika patenterade teknologiplattform. I juni 2020 noterades AegirBio på Nasdaq First North Growth Market. Bolagets ambition är, förutom att föra ut innovativ diagnostisk teknologi till marknaden, att göra diagnostik mer tillgänglig, enklare att använda och att ge korrekta och lätt överförbara resultat. För mer information, se Aegirbios hemsida www.aegirbio.com

Bolagets Certified Adviser är Eminova Fondkomission AB; adviser@eminova.se

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Hifab utser ny CFO

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Hifab utser Johan Lakfors till ny CFO, med ansvar för bolagets finans- och ekonomifrågor. Johan har arbetat på Hifab sedan november 2020, senast i rollen som Ekonomichef. Han har tidigare erfarenhet från roller som bland annat Financial Controller på Marginalen Bank, Ekonomichef på Porsche Center och Controller på GE Capital. 

Johan är och kommer fortsatt vara en del av Hifabs ledningsgrupp. Han tillträder rollen som CFO den 29 maj 2024.

För ytterligare information kontakta:

Emma Johansson
CMO & Kommunikationschef
073-072 37 66
emma.johansson@hifab.se

Nicke Rydgren
CEO
070-543 59 00
nicke.rydgren@hifab.se

Hifab är ett konsultbolag inom fastigheter och samhällsbyggnad. Vi erbjuder oberoende rådgivning och ledning där vi hjälper våra kunder med strategi i förändring, ledning i projekt och tekniska tjänster i drift och förvaltning. Hifab grundades 1947, omsätter 300 miljoner och finns representerade över hela Sverige. Läs mer på hifab.se.

Hifab är noterat på Nasdaq First North Growth Market och vår Certified Adviser är Mangold Fondkommission AB. Tel: +46 8 5030 1550. E-post: ca@mangold.se

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