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Lynparza in combination with abiraterone recommended for approval in the EU by CHMP as 1st-line treatment for patients with metastatic castration-resistant prostate cancer

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First PARP inhibitor to demonstrate clinical benefit in combination with a new hormonal agent in this setting.

AstraZeneca and MSD’s Lynparza (olaparib) in combination with abiraterone and prednisone or prednisolone has been recommended for marketing authorisation in the European Union (EU) for the treatment of adult patients with metastatic castration-resistant prostate cancer (mCRPC) for whom chemotherapy is not clinically indicated.

The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency based its positive opinion on results from the PROpel Phase III trial which were published in NEJM Evidence in June 2022.

In the trial, Lynparza in combination with abiraterone and prednisone or prednisolone, reduced the risk of disease progression or death by 34% versus abiraterone alone (based on a hazard ratio [HR] of 0.66; 95% confidence interval [CI] 0.54-0.81; p<0.0001). Median radiographic progression-free survival (rPFS) was 24.8 months for Lynparza plus abiraterone versus 16.6 months for abiraterone alone. Results also showed that Lynparza in combination with abiraterone extended median rPFS by almost one year, with a median rPFS of 27.6 months versus 16.4 with abiraterone alone, as assessed by blinded independent central review (BICR).

Updated results also showed a favourable trend in improved overall survival with Lynparza plus abiraterone versus abiraterone alone, however the difference did not reach statistical significance at the time of this data cut-off (analysis at 40% data maturity).

Prostate cancer is the most common cancer in men in Europe, with an estimated 473,000 patients diagnosed and 108,000 deaths in 2020.1-2 Overall survival for patients with mCRPC is approximately three years in clinical trial settings, and even shorter in real-world settings.3 Approximately half of patients with mCRPC may receive only one line of active treatment, with diminishing benefit of subsequent therapies.4-9

Noel Clarke, Urological Surgeon and Professor of Urological Oncology at Manchester’s Christie/Salford Royal Hospitals and Manchester University, the PROpel trial joint senior investigator, said: “Patients with metastatic castration-resistant prostate cancer in the European Union have limited treatment options. This form of advanced prostate cancer has a poor prognosis and treatment decisions after initial diagnosis are critical. If approved in the European Union for prostate cancer of this type, olaparib in combination with abiraterone will provide a much-needed new treatment option for the many men with this condition.”

Susan Galbraith, Executive Vice President, Oncology R&D, AstraZeneca, said: “With the incidence and mortality of prostate cancer set to double in the coming decades, it is more important than ever that we bring new treatment options to suitable patients at the earliest possible moment in their care. If approved, Lynparza in combination with abiraterone and prednisone or prednisolone will represent the first combination of a PARP inhibitor and new hormonal agent available to patients in the European Union.”

Eliav Barr, Senior Vice President, Head of Global Clinical Development and Chief Medical Officer, MSD Research Laboratories, said: “While prostate cancer has seen many advances in care in recent decades, for those with mCRPC, new treatment options are urgently needed. We are fully committed to bringing Lynparza in combination with abiraterone and prednisone or prednisolone to suitable patients in the European Union as quickly as possible.”

Lynparza in combination with abiraterone and prednisone or prednisolone is undergoing Priority Review in the US for the treatment of mCRPC in adult patients based on results from the PROpel Phase III trial, with a decision expected in Q4 2022.

Lynparza is approved in the US based on results from the PROfound Phase III trial as monotherapy for patients with homologous recombination repair (HRR) gene-mutated mCRPC (BRCA-mutated and other HRR gene mutations) who have progressed following prior treatment with enzalutamide or abiraterone; and in the EU, Japan, and China for patients with BRCA-mutated mCRPC who have progressed following prior therapy that included a new hormonal agent.

Notes

Metastatic castration-resistant prostate cancer
Metastatic prostate cancer is associated with a significant mortality rate.10 Development of prostate cancer is often driven by male sex hormones called androgens, including testosterone.11

In patients with mCRPC, their prostate cancer grows and spreads to other parts of the body despite the use of androgen-deprivation therapy to block the action of male sex hormones.5 Approximately 10-20% of men with advanced prostate cancer will develop castration-resistant prostate cancer (CRPC) within five years, and at least 84% of these men will have metastases at the time of CRPC diagnosis.5 Of patients with no metastases at CRPC diagnosis, 33% are likely to develop metastases within two years.5

Despite the advances in mCRPC treatment in the past decade with taxane and new hormonal agent (NHA) treatment, there is high unmet need in this population.5,7,8,12

PROpel
PROpel is a randomised, double-blind, multi-centre Phase III trial testing the efficacy, safety, and tolerability of Lynparza versus placebo when given in addition to abiraterone in men with mCRPC who had not received prior chemotherapy or NHAs in the mCRPC setting.

Men in both treatment groups also receive either prednisone or prednisolone twice daily. The primary endpoint is rPFS and secondary endpoints include overall survival, time to secondary progression or death, and time to first subsequent therapy.

In the PROpel Phase III trial, Lynparza is combined with abiraterone, an NHA which targets the androgen receptor (AR) pathway.

AR signalling engages a transcriptional programme that is critical for tumour cell growth and survival in prostate cancer.13,14 Preclinical models have identified interactions between PARP signalling and the AR pathway which support the observation of a combined anti-tumour effect of Lynparza and NHAs, like abiraterone, in both HRR deficient and HRR proficient prostate cancer.15-17

The PARP1 protein has been reported to be required for the transcriptional activity of androgen receptors; therefore, inhibiting PARP with Lynparza may impair the expression of androgen receptor target genes and enhance the activity of NHAs.13,16,18 Additionally, it is thought that abiraterone may alter/inhibit the transcription of some HRR genes which may induce HRR deficiency and increase sensitivity to PARP inhibition.15,17,19,20

For more information about the trial please visit ClinicalTrials.gov.

Lynparza
Lynparza (olaparib) is a first-in-class PARP inhibitor and the first targeted treatment to block DNA damage response (DDR) in cells/tumours harbouring a deficiency in HRR, such as those with mutations in BRCA1 and/or BRCA2, or those where deficiency is induced by other agents (such as NHAs).

Inhibition of PARP with Lynparza leads to the trapping of PARP bound to DNA single-strand breaks, stalling of replication forks, their collapse and the generation of DNA double-strand breaks and cancer cell death.

Lynparza is currently approved in a number of countries across multiple tumour types including maintenance treatment of platinum-sensitive relapsed ovarian cancer and as both monotherapy and in combination with bevacizumab for the 1st-line maintenance treatment of BRCA-mutated (BRCAm) and homologous recombination repair deficient (HRD)-positive advanced ovarian cancer, respectively; for gBRCAm, HER2-negative metastatic breast cancer (in the EU and Japan this includes locally advanced breast cancer); for gBRCAm, HER2-negative high-risk early breast cancer (in Japan this includes all BRCAm HER2-negative high-risk early breast cancer); for gBRCAm metastatic pancreatic cancer; and HRR gene-mutated metastatic castration-resistant prostate cancer (BRCAm only in the EU and Japan). In China, Lynparza is approved for the treatment of BRCA-mutated metastatic castration-resistant prostate cancer as well as a 1st-line maintenance therapy in BRCA-mutated advanced ovarian cancer.

Lynparza, which is being jointly developed and commercialised by AstraZeneca and MSD, has been used to treat over 75,000 patients worldwide. Lynparza has a broad clinical trial development programme, and AstraZeneca and MSD are working together to understand how it may affect multiple PARP-dependent tumours as a monotherapy and in combination across multiple cancer types. Lynparza is the foundation of AstraZeneca’s industry-leading portfolio of potential new medicines targeting DDR mechanisms in cancer cells.

The AstraZeneca and MSD strategic oncology collaboration
In July 2017, AstraZeneca and Merck & Co., Inc., Kenilworth, NJ, US, known as MSD outside the US and Canada, announced a global strategic oncology collaboration to co-develop and co-commercialise Lynparza, the world’s first PARP inhibitor, and Koselugo (selumetinib), a mitogen-activated protein kinase (MEK) inhibitor, for multiple cancer types.

Working together, the companies will develop Lynparza and Koselugo and other potential new medicines as monotherapies and as combinations. The companies will also develop Lynparza and Koselugo in combination with their respective PD-L1 and PD-1 medicines independently.

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, Rare Diseases, 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.   Rawla, P. The Epidemiology of Prostate Cancer. World J Oncol. 2019;10(2):63-89.

2.   IARC Globocan. Estimated number of incident cases and deaths Europe, both sexes, all ages (excl. NMSC). Available at https://gco.iarc.fr/today/online-analysis-multi-bars?v=2020&mode=cancer&mode_population=countries&population=900&populations=908&key=total&sex=0&cancer=39&type=0&statistic=5&prevalence=0&population_group=0&ages_group%5B%5D=0&ages_group%5B%5D=17&nb_items=10&group_cancer=1&include_nmsc=0&include_nmsc_other=1&type_multiple=%257B%2522inc%2522%253Atrue%252C%2522mort%2522%253Atrue%252C%2522prev%2522%253Afalse%257D&orientation=horizontal&type_sort=0&type_nb_items=%257B%2522top%2522%253Atrue%252C%2522bottom%2522%253Afalse%257D#collapse-group-0-4. Accessed November 2022

3.   Ng K, et al. Metastatic Hormone-Sensitive Prostate Cancer (mHSPC): Advances and Treatment Strategies in the First-Line Setting. Oncol Ther. 2020;8:209–230.

4.   de Wit R, et al. Real-world evidence of patients with metastatic castration-resistant prostate cancer treated with cabazitaxel: comparison with the randomized clinical study CARD. Prostate Cancer Prostatic. 2022;2660.

5.   Kirby M, et al. Characterising the castration-resistant prostate cancer population: systematic review. International Journal of Clinical Practice. 2021;65(11):1180-1192.

6.   Smith MR, et al. Natural history of rising serum prostate-specific antigen in men with castrate nonmetastatic prostate cancer. J Clin Oncol. 2005;23(13):2918-25.

7.   UroToday. What is Changing in Advanced Prostate Cancer? Available at https://www.urotoday.com/journal/everyday-urology-oncology-insights/articles/122176-what-is-changing-in-advanced-prostate-cancer.html. Accessed November 2022.

8.   Liu J, et al. Second-line Hormonal Therapy for the Management of Metastatic Castration-resistant Prostate Cancer: a Real-World Data Study Using a Claims Database. Scientific Report. 2020;10(4240):2020.

9.   Mateo J, et al. DNA-Repair Defects and Olaparib in Metastatic Prostate Cancer. N Engl J Med. 2015; 373:1697-1708.

10. Chowdhury S, et al. Real-world outcomes in first-line treatment of metastatic castration-resistant prostate cancer: the prostate cancer registry. Target Oncol. 2020;15(3):301-315.

11. Cancer.Net. Prostate Cancer: Types of Treatment. Available at https://www.cancer.net/cancer-types/prostate-cancer/types-treatment#:~:text=Chemotherapy%20may%20help%20those%20with,a%20set%20period%20of%20time. Accessed November 2022.

12. UroToday. Beyond First-line Treatment of Metastatic Castrate-resistant Prostate Cancer. Available at https://www.urotoday.com/library-resources/mcrpc-treatment/114592-beyond-first-line-treatment-of-metastatic-castrate-resistant-prostate-cancer.html. Accessed November 2022.

13. Schiewer MJ, et al. Dual roles of PARP-1 promote cancer growth and progression. Cancer Discov. 2012;2(12):1134-1149.

14. Schiewer MJ & Knudsen KE. AMPed up to treat prostate cancer: novel AMPK activators emerge for cancer therapy. EMBO Mol Med. 2014;6(4):439-441.

15. Li L, et al. Androgen receptor inhibitor–induced “BRCAness” and PARP inhibition are synthetically lethal for castration-resistant prostate cancer. Sci Signal. 2017; 10(480):eaam7479.

16. Polkinghorn WR, et al. Androgen receptor signaling regulates DNA repair in prostate cancers. Cancer Discov. 2013;3(11):1245-1253.

17. Asim M, et al. Synthetic lethality between androgen receptor signalling and the PARP pathway in prostate cancer. Nat Commun. 2017;374(8).

18. Ju B-G, et al. A topoisomerase IIbeta-mediated dsDNA break required for regulated transcription. Science. 2006;312(5781):1798-1802.

19. Goodwin JF, et al. A hormone-DNA repair circuit governs the response to genotoxic insult. Cancer Discov. 2013;3(11):1254-1271.

20. Tarish FL, et al. Castration radiosensitizes prostate cancer tissue by impairing DNA double-strand break repair. Sci Transl Med. 2015; 7(312):312re11.

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Marknadsnyheter

Nordea Bank Abp: Återköp av egna aktier den 05.12.2022

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Nordea Bank Abp
Börsmeddelande – Förändringar i återköpta aktier
05.12.2022 kl. 22.30 EET

Nordea Bank Abp (LEI-kod: 529900ODI3047E2LIV03) har den 05.12.2022 slutfört återköp av egna aktier (ISIN-kod: FI4000297767) enligt följande:

Handelsplats (MIC-kod)

Antal aktier

Viktad snittkurs/aktie, euro*, **

Kostnad, euro*, **

XHEL

260 000

 10,10

2 626 052,00

CEUX

240 000

 10,08

2 420 336,96

TQEX

36 000

 10,08

 362 819,55

XSTO

240 000

 10,07

2 416 602,28

XCSE

28 000

 10,10

 282 816,90

Summa

 804 000

 10,09

8 108 627,70

* Växelkurser som använts: SEK till EUR 10,9185 och DKK till EUR 7,4371
** Avrundat till två decimaler

Den 18 juli 2022 tillkännagav Nordea ett program för återköp av egna aktier till ett värde av högst 1,5 md euro med stöd av det bemyndigande som gavs av Nordeas ordinarie bolagsstämma 2022. Återköpet av egna aktier utförs genom offentlig handel i enlighet med Europaparlamentets och rådets förordning (EU) nr 596/2014 av den 16 april 2014 (marknadsmissbruksförordningen) och Kommissionens delegerade förordning (EU) 2016/1052.

Efter de redovisade transaktionerna innehar Nordea 11 832 125 egna aktier för kapitaloptimeringsändamål och 6 073 651 egna aktier för ersättningsändamål.

Uppgifter om respektive transaktion finns som en bilaga till detta meddelande.

För Nordea Bank Abp:s räkning,
Citigroup Global Markets Europe AG

För ytterligare information:

Matti Ahokas, chef för investerarrelationer, +358 9 5300 8011
Group Communication, +358 10 416 8023 eller [email protected]

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”Insikter om hot och våld” Del 2: Ett nytt, hårdare samtalsklimat

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Vad som många har en diffus känsla av stämmer – samtalsklimatet mellan medborgare och samhällets företrädare HAR blivit hårdare. Detta är ett vetenskapligt belagt faktum och det finns en tydlig koppling till hur samtalstonen på nätet har utvecklats. 

Måns Svensson är professor i rättssociologi, vilket förenklat kan beskrivas som kunskapen om hur sociala normer samspelar med lagstiftningen. Under senare tid har Svensson forskat kring utvecklingen av näthat och hur det påverkat kommunikationen mellan allmänhet och olika samhällsföreträdare, exempelvis förtroendevalda, journalister, lärare och vårdanställda.  

– Den här typen av ogillande som samhällets representanter utsätts för visar att den sociala kontrollen har förändrats i grunden, vilket är ett resultat av hur vi kommunicerar online. Vi har tillgång till varandra och kan uttrycka ogillande på ett sätt som är helt nytt. 

Intervjun med Måns Svensson är del två i Säker Vårdmiljös intervjuserie ”Insikter om hot och våld”. Seriens ambition är att lyfta fram insikter, perspektiv och lärdomar på ett ämne som tyvärr blir alltmer aktuellt.  

Du hittar filmerna i serien här:
https://vimeo.com/showcase/9940451

Säker Vårdmiljö startar under hösten även ett kunskapsnätverk som fokuserar på problematiken med hot och våld. Intresserad? Anmäl dig här. 

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Marknadsnyheter

Återköp av aktier i MTG under vecka 48, 2022

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Från 28 november till 2 december 2022 har Modern Times Group MTG AB (publ) (LEI-kod 549300E8NDODRSX29339) (“MTG”) återköpt sammanlagt 166 437 egna aktier av serie B (ISIN-kod: SE0018012494) inom ramen för det återköpsprogram som styrelsen infört i syfte att leverera värde till bolagets aktieägare och optimera kapitalstrukturen.

Återköpen är en del av det återköpsprogram om maximalt 4 618 818 aktier till ett sammanlagt belopp om högst 400 miljoner kronor som MTG tillkännagav den 25 oktober 2022. Återköpsprogrammet löper från den 27 oktober 2022 och fram till årsstämman 2023 och genomförs i enlighet med EU:s Marknadsmissbruksförordning (EU) nr 596/2014 (”MAR”) och Kommissionens delegerade förordning (EU) nr 2016/1052 (”Safe harbour-förordningen”). Syftet med återköpsprogrammet är att leverera värde till aktieägare och att optimera kapitalstrukturen. Avsikten är att MTG:s aktiekapital ska nedsättas genom en indragning av återköpta aktier.

Aktier av serie B i MTG har återköpts (i kronor) enligt följande:

Datum Aggregerad daglig volym (antal aktier) Viktat genomsnittspris per dag (SEK) Totalt dagligt transaktionsvärde (SEK)
2022-11-28 35 587 83,0867 2 956 806,39
2022-11-29 35 000 83,0586 2 907 051,00
2022-11-30 33 851 82,3301 2 786 956,22
2022-12-01 35 149 82,8424 2 911 827,52
2022-12-02 26 850 83,7622 2 249 015,07

Samtliga förvärv har genomförts på Nasdaq Stockholm av Nordea Bank Abp för MTG:s räkning. Efter ovanstående förvärv uppgår MTG:s innehav av egna aktier per den 2 december 2022 till 3 347 283 aktier av serie B och 6 324 343 aktier av serie C. Det totala antalet aktier i MTG uppgår till 134 035 940.

Fullständig information om de genomförda transaktionerna enligt artikel 5.3 i MAR och artikel 2.3 i Safe harbour-förordningen biläggs detta pressmeddelande.

För mer information:

Anton Gourman, VP Communications and IR
Direkt: +46 73 661 8488, 
[email protected]

Följ oss: mtg.com / Twitter / LinkedIn

Om MTG

MTG (Modern Times Group MTG AB (publ.)) (www.mtg.com) är en internationell mobilspelskoncern som äger och driver spelutvecklare med globalt populära titlar som sträcker sig över en bred uppsättning genrer inom casual- och mid-core-spel. Koncernen fokuserar på att accelerera portföljbolagens tillväxt och stödja grundare och entreprenörer. MTG är en aktiv aktör i den pågående konsolideringen av spelindustrin och en strategisk köpare av gamingbolag världen runt. Vi kommer från Sverige men har en internationell kultur och globalt fotavtryck. Våra aktier är noterade på Nasdaq Stockholm under symbolerna MTGA och MTGB.

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