AstraZeneca advances leadership in renal disease with more than 80 abstracts at ASN Kidney Week 2020 Reimagined
AstraZeneca advances leadership in renal disease
with more than 80 abstracts at ASN Kidney Week 2020 Reimagined
For roxadustat, more than 40 abstracts present safety and efficacy
outcomes in anaemia of chronic kidney disease
For Farxiga, new subgroup data from the DAPA-CKD Phase III trial assesses the
potential benefit irrespective of the cause of chronic kidney disease
Data demonstrate progress towards helping prevent or slow the progression
of chronic kidney disease and address life-threatening complications
20 October 2020
AstraZeneca will present 84 abstracts, including 12 oral presentations and three late-breaking abstracts, across its industry-leading renal portfolio which includes roxadustat, Farxiga (dapagliflozin) and Lokelma (sodium zirconium cyclosilicate), at ASN Kidney Week 2020 Reimagined, taking place virtually from 22-25 October 2020.
The data advance AstraZeneca’s ambition to create a coordinated pathway for renal patients to advance earlier diagnosis and help prevent or slow the progression of chronic kidney disease (CKD) and address its life-threatening complications, such as anaemia and hyperkalaemia.1,2
Roxadustat - redefining the management of anaemia of CKD
More than 40 abstracts will be presented on roxadustat, a first-in-class oral hypoxia-inducible-factor prolyl hydroxylase inhibitor (HIF-PHI). The abstracts provide new insights on the potential of the medicine to transform the standard of care in anaemia of CKD across key patient sub-populations, notably:
· Late-breaking presentations of pooled analyses of Phase III trials investigating the association between haemoglobin levels and CV outcomes in dialysis-dependent (DD) and non-dialysis dependent (NDD)-CKD patients. Cardiovascular (CV) outcomes are common and serious complications in patients with CKD.3-5
· An oral presentation exploring whether roxadustat can reduce the risk of hospitalisation for heart failure, a common comorbidity in patients with CKD.6
· Analyses of whether roxadustat has the potential to reduce the risk of red blood cell (RBC) transfusions, a treatment for anaemia associated with additional complications, in both DD-CKD and NDD-CKD patients.7
· An analysis exploring the effect of roxadustat on achieving haemoglobin levels ≥10 g/dL in patients with NDD-CKD.8
· New data from pooled analyses of Phase III trials on DD-CKD patient subgroups, including those who are receiving peritoneal dialysis and are new to dialysis.9,10
Farxiga - setting a new standard in early CKD protection
New late-breaking subgroup data from the ground-breaking DAPA-CKD Phase III trial evaluating the potential benefit of Farxiga in patients with CKD irrespective of the underlying cause.11 Detailed results presented in August and published in The New England Journal of Medicine established Farxiga as the first medicine to significantly prolong survival in a renal outcomes trial in patients with CKD with and without type-2 diabetes (T2D).
Lokelma - advancing proactive potassium management
New sub-analyses of the DIALIZE Phase IIIb trial and real-world evidence in patients living with CKD and hyperkalaemia demonstrate the potential of Lokelma as an option for hyperkalaemia management.12-14 Hyperkalaemia is a common complication in patients with CKD and can result in serious arrhythmias, sudden cardiac arrest, paralysis and weakness, and even death.2,15,16 If not managed effectively, complications like hyperkalaemia can impact ongoing treatment approaches, leading to life-saving treatments being reduced or discontinued.16
Uncovering the unique unmet needs of the CKD patient community
AstraZeneca will also present new insights into patients’ experiences living with CKD as well as actionable gaps in treatment and management. New data will be presented from DISCOVER-CKD, a trial that assesses current real-world practice patterns and clinical management of patients with CKD. It reveals the burden of disease and factors that determine poor clinical outcomes, underscoring the need for improved treatment options.17
AstraZeneca key abstracts at ASN Kidney Week 2020 include:
Lead author |
Abstract title |
Presentation details |
Roxadustat |
||
Provenzano, R. |
Associations between Achieved Hemoglobin and Cardiovascular Outcomes in the Pooled Phase 3 Trials of Roxadustat in Dialysis-dependent Patients with Anemia of Chronic Kidney Disease |
ePoster #PO2626 22 October
|
Fishbane, S. |
Associations between Achieved Hemoglobin and Cardiovascular Outcomes in the Pooled Phase 3 Trials of Roxadustat in Non-Dialysis-dependent Patients with Anemia of Chronic Kidney Disease |
ePoster #PO2625 22 October |
Provenzano, R. |
Roxadustat Treatment of Anemia in Non-Dialysis-Dependent Chronic Kidney Disease is Not Influenced by Iron Status |
Oral Abstract #TH-OR03 22 October 17:00 – 19:00 PM EDT
|
Fishbane, S.
|
Roxadustat Lowers Risk of RBC Transfusion in Patients with Anemia in CKD |
ePoster #PO0256 22 October |
Pergola, P.E. |
Hemoglobin (Hb) correction with roxadustat is associated with improved iron homeostasis in patients with dialysis-dependent chronic kidney disease (DD-CKD) |
Oral Abstract #TH-OR06 22 October 5:00 – 7:00 PM EDT
|
El-Shahawy, M. |
Roxadustat Increases Hemoglobin in Anemic Dialysis-Dependent (DD) Chronic Kidney Disease (CKD) Patients Independent of Inflammation |
ePoster #PO0265 22 October |
Pecoits-Filho, R. |
Roxadustat treatment results in consistent improvements in hemoglobin (Hb) versus placebo: an analysis of 3 multinational RCTs in patients with non-dialysis-dependent chronic kidney disease (NDD-CKD) |
Oral Abstract #TH-OR05 22 October 17:00 – 19:00 PM EDT
|
Rastogi, A. |
Roxadustat treatment corrects anemia to hemoglobin (Hb) values ≥10 g/dL in the majority of patients with non-dialysis-dependent chronic kidney disease (NDD-CKD) |
ePoster #PO0264 22 October |
Pollock, C.A.
|
Roxadustat Increases Hemoglobin in Anemic Non-Dialysis-Dependent (NDD) Chronic Kidney Disease (CKD) Patients Independent of Inflammation |
ePoster #PO0263 22 October |
Provenzano, R. |
Pooled Analyses of the Phase 3 Roxadustat Studies: Congestive Heart Failure Hospitalization Rates in Dialysis and Non-Dialysis Patients with Anemia treated with Roxadustat versus Comparators |
Oral Abstract #SA-OR39 24 October 17:00 – 19:00 PM EDT
|
Provenzano, R. |
Efficacy and Safety of Roxadustat in Patients with Dialysis-dependent Chronic Kidney Disease and Anemia on Hemodialysis |
Oral Abstract #FR-OR25 23 October 17:00 – 19:00 PM EDT
|
Chan, T.M. |
Efficacy and Safety of Roxadustat in Patients with Dialysis-dependent Chronic Kidney Disease and Anemia on Peritoneal Dialysis |
Oral Abstract #SU-OR24 25 October 17:00 – 19:00 PM EDT
|
Lopes, M. |
A Real World Longitudinal Analysis of Anemia Treatment Prescriptions in Non-Dialysis-Dependent Chronic Kidney Disease Patients, a CKDopps Study |
Oral Abstract #TH-OR10 22 October 17:00 – 19:00 PM EDT
|
Barratt, J. |
Roxadustat for the Treatment of Anemia in Chronic Kidney Disease (CKD) Patients Not on Dialysis (NDD): A Phase 3, Randomized, Open-Label, Active-Controlled Study |
Oral Abstract #TH-OR02 22 October 17:00 – 19:00 PM EDT
|
Provenzano, R.
|
Adverse Event Rates are Higher Post-transfusion vs. Overall Follow-up and Independent of Background Anemia Treatment in Patients with Chronic Kidney Disease |
Oral Abstract #TH-OR09 22 October 17:00 – 19:00 PM EDT
|
Coyne, D.W. |
Roxadustat Is Not Associated with An Increased Risk of Neoplasm in Patients with Chronic Kidney Disease and Anemia |
Oral Abstract #TH-OR04 22 October 17:00 – 19:00 PM EDT
|
Provenzano, R.
|
Subgroup Analyses of Efficacy of Roxadustat for Treatment of Anemia in Patients with Incident–Dialysis-dependent Chronic Kidney Disease |
ePoster #PO0260 22 October |
Farxiga |
||
Wheeler, D.C. |
Effects of dapagliflozin on kidney function, cardiovascular events and all-cause mortality according to cause of kidney disease in the DAPA-CKD trial |
Oral Abstract #FR-OR58 23 October 10:30 AM – 12:30 PM EDT |
Heerspink, H.J.L.
|
Effects of the SGLT2 Inhibitor Dapagliflozin on Proteinuria in Non-Diabetic Patients with Chronic Kidney Disease (DIAMOND): A Randomized Double-Blind Cross-Over Trial |
ePoster #PO0588 22 October
|
McEwan, P.
|
The impact of decline in renal function on the clinical and economic burden of chronic kidney disease: an application of the DAPA-CKD cost-effectiveness model |
ePoster #PO0589 22 October |
Birkeland, K.I. |
Lower Cardiorenal Risk with SGLT2i versus DPP4i in T2D Patients without Established Cardiovascular- and Renal Diseases: A Large Multinational Observational Study |
ePoster #PO0954 22 October |
Lokelma |
||
Spinowitz, B. |
Disease course of hyperkalemia in patients on hemodialysis |
ePoster #PO1165 22 October |
Fishbane, S. |
Risk of Hypokalemia in Hyperkalemic Hemodialysis Patients |
ePoster #PO1051 22 October |
Tafesse, E. |
Hyperkalaemia risk and mortality in patients with diabetes |
ePoster #PO0968 22 October |
Tafesse, E. |
The relationship between chronic kidney disease duration, serum potassium level and adverse outcomes |
ePoster #PO1450 22 October |
Tafesse, E. |
The relationship between comorbidities and hyperkalaemia in patients with CKD |
ePoster #PO1448 22 October |
James, G. |
Patient palatability and preference study of 3 potassium binders in patients with chronic kidney disease and hyperkalemia: rationale and design of the APPETIZE study |
ePoster #PO1456 22 October |
Israni, R. |
Patient and Clinician Preferences for Hyperkalemia Treatment: A Qualitative Study |
ePoster #PO1455 22 October |
Hsuing, J.T. |
Time to Hyperkalemia Recurrence in One Year among 103,155 US Veterans |
ePoster #PO2054 22 October |
Kanda, E. |
Performance of machine learning models for risk prediction of adverse events in hyperkalemic patients |
ePoster #PO1453 22 October |
Davis, J. |
Post-discharge outcomes among hyperkalemic patients treated with and without SPS in the inpatient setting |
ePoster #PO1445 22 October |
Perez-Navarro, L.M. |
Prevalence and severity of hyperkalemia in patients referred to nephrology consultation. Epidemiologic data from 1106 Mexican patients at a national reference hospital. |
ePoster #PO0479 22 October |
DISCOVER-CKD |
||
Wittbrodt, E. |
Baseline characteristics of non-dialysis CKD patients with and without anemia: a report from the retrospective cohort from DISCOVER CKD |
ePoster #PO0486 22 October |
Wittbrodt, E. |
Treatment pathways of non-dialysis dependent CKD patients with anemia: A report from the DISCOVER CKD retrospective cohort |
ePoster #PO0287 22 October |
Garcia-Sanchez, J.J. |
Healthcare resource utilisation and costs of chronic kidney disease according to the 2012 KDIGO CKD classification: A Report from the DISCOVER CKD Retrospective Cohort |
ePoster #PO0498 22 October |
Cotadutide |
||
Parker, V.E.R. |
Efficacy and safety of cotadutide, a dual GLP-1 and glucagon receptor agonist, for patients with type 2 diabetes mellitus and chronic kidney disease |
ePoster #PO1018 22 October |
General CKD |
||
James, G. |
Development of a Global Chronic Kidney Disease-Personal Impact Index (CKD-PII) Assessing the Reality of Living with CKD |
ePoster #PO0577 22 October |
ASN Kidney Week 2020 abstracts are available online.
Roxadustat
Roxadustat is a first-in-class oral small molecule hypoxia-inducible-factor prolyl hydroxylase inhibitor (HIF-PHI) that promotes erythropoiesis through increased endogenous production of erythropoietin; improved iron absorption, transport and mobilisation; and downregulation of hepcidin, which helps to overcome the negative impact of inflammation on haemoglobin synthesis and red blood cell production. Roxadustat is approved in China for the treatment of anaemia in adult patients with CKD, both on dialysis and not on dialysis. In Japan, roxadustat is approved for the treatment of anaemia in CKD patients on dialysis, and a supplemental New Drug Application (NDA) for the treatment of anaemia in CKD patients not on dialysis is under regulatory review. The roxadustat NDA for the treatment of anaemia in CKD in both NDD and DD is under review by the US Food and Drug Administration with a decision expected in Q4 2020. The Marketing Authorisation Application for roxadustat for the treatment of anaemia in CKD in both NDD and DD was filed by Astellas and accepted by the European Medicines Agency for review on 21 May 2020. Roxadustat is also in clinical development for anaemia associated with myelodysplastic syndromes (MDS) and for chemotherapy-induced anaemia (CIA).
AstraZeneca and FibroGen Inc. (FibroGen) are collaborating on the development and commercialisation of roxadustat for the potential treatment of anaemia in the US, China and other markets in the Americas and in Australia/New Zealand, as well as Southeast Asia. Astellas and FibroGen are collaborating on the development and commercialisation of roxadustat for the potential treatment of anaemia in territories including Japan, Europe, the Commonwealth of Independent States, the Middle East and South Africa. At ASN Kidney Week 2020 Reimagined, roxadustat data will be sponsored and presented by Astellas, AstraZeneca and FibroGen.
Farxiga
Farxiga (dapagliflozin) is a first-in-class, oral, once-daily sodium-glucose co-transporter-2 inhibitor indicated in adults for the treatment of insufficiently controlled T2D as both monotherapy and as part of combination therapy as an adjunct to diet and exercise to improve glycaemic control, with the additional benefits of weight loss and blood-pressure reduction. In the DECLARE CV outcomes trial in adults with T2D, Farxiga reduced the risk of the composite endpoint of hospitalisation for heart failure (hHF) or CV death versus placebo, when added to standard of care.
In May 2020, Farxiga was approved in the US to reduce the risk of CV death and hHF in adults with heart failure (HF) (NYHA class II-IV) with reduced ejection fraction (HFrEF) with and without T2D. In the DAPA-CKD Phase III trial in patients with CKD, Farxiga met all primary and secondary endpoints, providing overwhelming efficacy. Farxiga is currently being tested for patients with HF in the DELIVER (HF with preserved ejection fraction, HFpEF) and DETERMINE (HFrEF and HFpEF) trials. Farxiga will also be tested in patients without T2D following an acute myocardial infarction (MI) or heart attack in the DAPA-MI trial – a first of its kind, indication-seeking registry-based randomised controlled trial. Farxiga has a robust programme of clinical trials that includes more than 35 completed and ongoing Phase IIb/III trials in more than 35,000 patients, as well as more than 2.5 million patient-years’ experience.
Lokelma
Lokelma (sodium zirconium cyclosilicate) is an insoluble, non-absorbed sodium zirconium silicate, formulated as a powder for oral suspension, that acts as a highly selective potassium-removing medicine. It is administered orally, is odourless, tasteless and stable at room temperature. It has been studied in three double-blind, placebo-controlled trials and one 12-month open-label clinical trial in patients with hyperkalaemia.
AstraZeneca in CVRM
Cardiovascular, Renal and Metabolism (CVRM) together forms one of AstraZeneca’s three therapy areas and is a key growth driver for the Company. By following the science to understand more clearly the underlying links between the heart, kidneys and pancreas, AstraZeneca is investing in a portfolio of medicines to protect organs and improve outcomes by slowing disease progression, reducing risks and tackling comorbidities. The Company’s ambition is to modify or halt the natural course of CVRM diseases and potentially regenerate organs and restore function, by continuing to deliver transformative science that improves treatment practices and cardiovascular health for millions of patients worldwide.
AstraZeneca (LSE/STO/Nasdaq: AZN) is a global, science-led biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines, primarily for the treatment of diseases in three therapy areas - Oncology, 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.
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References
1. KDOQI Clinical Practice Guidelines and Clinical Practice Recommendations for Anemia in Chronic Kidney Disease. Am J Kidney Dis 2006; 47(5 Suppl 3):S1-146.
2. National Kidney Foundation. Clinical Update on Hyperkalemia: A chronic Risk for CKD Patients and a Potential Barrier to Recommended CKD Treatment. New York: National Kidney Foundation; 2014 [cited 16 October 2020]. Available from: URL: https://www.kidney.org/sites/default/files/02-10-6785_HBE_Hyperkalemia_Bulletin.pdf.
3. Fishbane S et al. Associations between Achieved Hemoglobin and Cardiovascular Outcomes in the Pooled Phase 3 Trials of Roxadustat in Dialysis-dependent Patients with Anemia of Chronic Kidney Disease. Abstract #PO2625 presented at: American Society of Nephrology - Kidney Week 2020 Reimagined, 19-25 October 2020.
4. Provenzano R et al. Associations between Achieved Hemoglobin and Cardiovascular Outcomes in Phase 3 Roxadustat Studies of Non dialysis-dependent Patients with Anemia of Chronic Kidney Disease. Abstract # #PO2626 presented at: American Society of Nephrology - Kidney Week 2020 Reimagined, 19-25 October 2020.
5. Centers for Disease Control and Prevention (CDC). Chronic Kidney Disease: Common - Serious - Costly; 12 December 2019 [cited 16 October 2020]. Available from: URL: https://www.cdc.gov/kidneydisease/prevention-risk/CKD-common-serious-costly.html.
6. Provenzano R et al. Pooled Analyses of the Phase 3 Roxadustat Studies: Congestive Heart Failure Hospitalization Rates in Dialysis and Non-Dialysis Patients with Anemia treated with Roxadustat versus Comparators. Abstract #SA-OR39 presented at: American Society of Nephrology - Kidney Week 2020 Reimagined, 19-25 October 2020.
7. Fishbane S et al. Roxadustat Lowers Risk of RBC Transfusion in Patients with Anemia in CKD. Abstract #PO0256 presented at: American Society of Nephrology - Kidney Week 2020 Reimagined, 19-25 October 2020.
8. Rastogi, A et al. Roxadustat treatment corrects anemia to hemoglobin (Hb) values ≥10 g/dL in the majority of patients with non-dialysis-dependent chronic kidney disease (NDD-CKD). Abstract #PO0264 presented at: American Society of Nephrology - Kidney Week 2020 Reimagined, 19-25 October 2020.
9. Chan, TM et al. Efficacy and Safety of Roxadustat in Patients with Dialysis-dependent Chronic Kidney Disease and Anemia on Peritoneal Dialysis. Oral #SU-OR24 presented at: American Society of Nephrology - Kidney Week 2020 Reimagined, 19-25 October 2020.
10. Provenzano R et al. Subgroup Analyses of Efficacy of Roxadustat for Treatment of Anemia in Patients with Incident–Dialysis-dependent Chronic Kidney Disease Abstract #PO0259 presented at: American Society of Nephrology - Kidney Week 2020 Reimagined, 19-25 October 2020.
11. Wheeler D. Effects of dapagliflozin on kidney function, cardiovascular events and all-cause mortality according to cause of kidney disease in the DAPA-CKD trial. Abstract #FR-OR58 presented at: American Society of Nephrology - Kidney Week 2020 Reimagined, 19-25 October 2020.
12. Fishbane S. Risk of Hypokalemia in Hyperkalemic Hemodialysis Patients. Abstract #PO1051 presented at: American Society of Nephrology - Kidney Week 2020 Reimagined, 19-25 October 2020.
13. Tafesse E, James G, Sugrue D, Hurst M, Hoskin L, Badora K, McEwan P. The relationship between comorbidities and hyperkalaemia in patients with chronic kidney disease. Abstract #PO1448 presented at: American Society of Nephrology - Kidney Week 2020 Reimagined, 19-25 October 2020.
14. Tafesse E, James G, Hurst M, Hoskin L, Badora K, Sugrue D, McEwan P. The relationship between chronic kidney disease duration, serum potassium level and adverse outcomes. Abstract #PO1450 presented at: American Society of Nephrology - Kidney Week 2020 Reimagined, 19-25 October 2020.
15. American Heart Association. Part 10.1: Life-Threatening Electrolyte Abnormalities. Circulation 2005; 112(24_suppl):IV-121-IV-125.
16. Montford JR et al. How Dangerous is Hyperkalaemia? J Am Soc Nephrol. 2017 Nov;28(11):3155-3165.
17. U.S. National Institutes of Health. A Study on Patients With Chronic Kidney Disease (CKD) to Assess Treatment Experience and Patterns, Effect of the Treatment, Patient Outcomes and Patient Quality of Life (DISCOVER CKD) [Identifier: NCT04034992] [cited 16 October 2020]. Available from: URL: https://clinicaltrials.gov/ct2/show/NCT04034992.
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