Pharmacokinetics and safety of olaparib in patients with advanced solid tumours and mild or moderate hepatic impairment

Author:

Rolfo Christian1ORCID,Isambert Nicolas2,Italiano Antoine3,Molife L. Rhoda4,Schellens Jan H.M.56,Blay Jean‐Yves7,Decaens Thomas8,Kristeleit Rebecca9,Rosmorduc Olivier10,Demlova Regina11,Lee Myung‐Ah12,Ravaud Alain13,Kopeckova Katerina14,Learoyd Maria15,Bannister Wendy16,Locker Gershon17,Vos‐Geelen Judith18

Affiliation:

1. Marlene and Stewart Greenebaum Comprehensive Cancer Center, Experimental Therapeutics Program University of Maryland School of Medicine Baltimore Maryland USA

2. Centre Georges François Leclerc Dijon France

3. Institut Bergonié, Gironde France

4. *Royal Marsden Hospital London UK

5. The Netherlands Cancer Institute Amsterdam The Netherlands

6. Utrecht Institute for Pharmaceutical Sciences (UIPS) Utrecht University Utrecht The Netherlands

7. Centre Léon Bérard Lyon France

8. Department of hepato‐gastroenterology, Université Grenoble‐Alpes, CHU Grenoble‐Alpes Institute for Advanced Biosciences Grenoble France

9. The Netherlands Cancer Institute, Amsterdam and Utrecht University Utrecht The Netherlands

10. APHP, Hôpital La Pitié Salpêtrière Service d'Hépato‐Gastroentérologie Paris France

11. Faculty of Medicine, Department of Pharmacology Masaryk Memorial Cancer Institute, Masaryk Univerzity Brno Czech Republic

12. The Catholic University of Korea, Seoul St. Mary's Hospital Seoul South Korea

13. Hôpital Saint André Bordeaux University Hospital Bordeaux France

14. University Hospital in Motol, Charles University Prague Czech Republic

15. AstraZeneca Cambridge UK

16. Phastar London UK

17. AstraZeneca Gaithersburg MD USA

18. Department of Internal Medicine, Division of Medical Oncology, GROW—School for Oncology and Developmental Biology Maastricht University Medical Center Maastricht The Netherlands

Funder

AstraZeneca

Merck Sharp and Dohme

Merck

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

Reference29 articles.

1. Olaparib: an oral PARP-1 and PARP-2 inhibitor with promising activity in ovarian cancer

2. European Medicines Agency.Lynparza (olaparib): An overview of Lynparza and why it is authorised in the EU.2019. Available at:https://www.ema.europa.eu/en/documents/overview/lynparza-epar-medicine-overview_en.pdf.

3. European Medicines Agency.Lynparza summary of product characteristics.2014. Available at:http://www.ema.europa.eu/docs/en_GB/document_library/EPAR_-_Product_Information/human/003726/WC500180151.pdf

4. FDA.Lynparza prescribing information.2014. Available at:https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/206162lbl.pdf.

5. European Medicines Agency.CHMP assessment report on extension of marketing authorisation grouped with a variation: Lynparza.2018. Available at:http://www.ema.europa.eu/docs/en_GB/document_library/EPAR_-_Assessment_Report_-_Variation/human/003726/WC500249582.pdf

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