GlaxoSmithKline plc (LSE/NYSE: GSK) today announced positive headline results from five studies of the Phase 3 ASCEND programme, evaluating the efficacy and safety profile of daprodustat, an investigational oral hypoxia-inducible factor prolyl hydroxylase inhibitor (HIF-PHI),?for patients with anaemia?due to chronic kidney disease?(CKD). The ASCEND programme showed that daprodustat met its primary efficacy endpoint in each study, demonstrating an improvement in haemoglobin (Hgb) levels in untreated patients and maintaining Hgb levels in patients treated with an erythropoietin stimulating agent (ESA), a standard treatment option, in patients?with anaemia of CKD. In addition, the key cardiovascular outcomes studies for non-dialysis?(ASCEND-ND) and dialysis patients (ASCEND-D) demonstrated that daprodustat was non-inferior when compared to?an ESA?in the risk of Major Adverse Cardiovascular Events (MACE), the co-primary endpoint of both studies. Dr. Hal Barron, Chief Scientific Officer and President R&D,?GSK, said:??I am particularly pleased?with the results from the ASCEND-ND and ASCEND-D studies given the importance of managing cardiovascular outcomes for patients who are currently suffering from anaemia due to chronic kidney disease, as well as the need to provide a convenient, oral treatment option. We will continue to analyse the data from the robust phase 3 ASCEND programme and look forward to working closely with regulators as we plan for our submissions.? In addition to the ASCEND-D and ASCEND-ND studies, the programme also included studies focused on incident dialysis, for patients just starting dialysis (ASCEND-ID); quality of life measures (ASCEND-NHQ); as well as three-times weekly dosing regimens (ASCEND-TD). Each of the studies from the programme met its respective primary or co-primary endpoint(s). The programme enrolled over 8,000 patients who were treated for up to 3.75 years. The full results of the studies will be presented at a forthcoming medical meeting later this year and will be used to inform regulatory pathways with health authorities worldwide. Across the ASCEND programme, daprodustat was generally well tolerated in both non-dialysis and dialysis patients.?The incidence of treatment-emergent adverse events was similar between treatment groups and the nature of reported events was consistent with the underlying patient population. The most commonly reported adverse events in patients receiving daprodustat across the ASCEND programme included hypertension, diarrhoea, dialysis hypotension, peripheral edema, and urinary tract infection. Daprodustat is currently approved in Japan as Duvroq for patients with renal anaemia. It is not approved anywhere else in the world. About Anaemia of CKD Chronic kidney disease, characterised by progressive loss of kidney function, is an increasing global public health burden.^[1]?Risk factors for CKD include hypertension, diabetes, obesity and primary renal disorders.^[1]?Furthermore, CKD is an independent risk factor for cardiovascular disease.^[1]?Anaemia is an important and frequent complication of CKD.^[2]?However, it is often poorly diagnosed and undertreated in patients with early stage CKD, such as those not on dialysis.^[2]?When left untreated or undertreated, anaemia of CKD is associated with poor clinical outcomes and leads to a substantial burden on patients and healthcare systems.^[2] About daprodustat Daprodustat, an oral hypoxia-inducible factor prolyl hydroxylase inhibitor (HIF-PHI), belongs to a novel class of oral medicines indicated for the treatment of anaemia due to chronic kidney disease in adult patients not on dialysis and on dialysis. Inhibition of oxygen-sensing prolyl hydroxylase enzymes stabilises hypoxia-inducible factors, which can lead to transcription of erythropoietin and other genes involved in the correction of anaemia, similar to the physiological effects that occur in the body at high altitude. Daprodustat has been developed to provide a convenient oral treatment option for patients with anaemia associated with CKD. About GSK GSK is a science-led global healthcare company. For further information please visit?www.gsk.com/about-us. Cautionary statement regarding forward-looking statements GSK cautions investors that any forward-looking statements or projections made by GSK, including those made in this announcement, are subject to risks and uncertainties that may cause actual results to differ materially from those projected. Such factors include, but are not limited to, those described in the Company's Annual Report on Form 20-F for 2020 and any impacts of the COVID-19 pandemic. 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Cross-sectional survey in CKD patients across Europe describing the association between quality of life and anaemia.?BMC Nephrol.?2016;17(1):97. van Haalen H, Jackson J, Spinowitz B, et al. Impact of chronic kidney disease and anemia on health-related quality of life and work productivity: analysis of multinational real-world data.?BMC Nephrol.?2020;21(1):88. Eriksson D, Teitsson S, Goldsmith D, et al. Cross-sectional descriptive study of the impact of anaemia in patients with chronic kidney disease on healthcare resource utilisation and work productivity across Europe.?Value Health.?2015;18(A514).