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Treatmentupdate 223 Vol
TreatmentUpdate 223 Vol. 29, No. 5 · December 2017 Available online at www.catie.ca/en/treatmentupdate Contents G. Canakinumab’s anti-cancer potential 10 I INFLAMMATION AND HIV H. Issues to consider with canakinumab 12 A. Exploring HIV and inflammation 2 I. Canakinumab in HIV reduces B. Inflammation in arteries vs. inflammation 13 lymph nodes 5 J. The potential of Ixolaris 15 C. Pitavastatin found to reduce levels of bad cholesterol and inflammation 6 K. Clinical trials in Canada to explore reducing inflammation in HIV 16 D. Inflammation-related illness among HIV-positive people 7 L. suPAR—an early warning signal 16 E. Why is there renewed interest in the antibody canakinumab? 8 F. Canakinumab—effect on reducing inflammation and heart attacks in the Cantos study 9 produced by 555 Richmond Street West, Suite 505 Box 1104 Toronto, Ontario M5V 3B1 Canada phone: 416.203.7122 toll-free: 1.800.263.1638 fax: 416.203.8284 www.catie.ca charitable registration number: 13225 8740 RR Page 2 TreatmentUpdate 223 — Vol. 29 No. 5 __________________________________________________________ I INFLAMMATION AND HIV Why is persistent immune activation and inflammation important? A. Exploring HIV and inflammation The activation of the immune system and inflammation are important responses used by Chronic HIV infection is associated with relatively the immune system to help control infections and high levels of inflammation and a growing body tumours. However, researchers are concerned that of evidence suggests that inflammation may prolonged immune activation and inflammation increase the risk for a range of health problems. could slowly degrade vital organ-systems in the body. -
Proposal for Assessment of New Health Technologies
v4.0 11.12.2017 Proposal for assessment of new health technologies Important information – read this first! Submitted proposals for national health technologies (HTAs) will be published in full. If the proposer thinks there is information necessary for filling out the form, that should not be made public, please contact the secretariat (Nye Metoder) before submission. The proposer is aware that the form will be published in its entirety (tick): ☒ Proposer has filled out point 19 below «Interests and, if any, conflicts of interest» (tick): ☒ This form serves the purpose to submit proposals for health technology assessment (HTA) at the national level in Nye Metoder - the national system for managed introduction of new health technologies within the specialist health service in Norway. The form does not apply to proposals for research projects. A health technology assessment is a type of evidence review, and for this to be possible, documentation is required, e.g. from completed clinical trials. Lack of documentation may be one of the reasons why the Commissioning Forum (Bestillerforum RHF) does not assign a health technology assessment. If the proposal concerns a medical device, the proposer is familiar with the document «Guidance criteria for management of medical devices in the National System for Managed Introduction of New Health Technologies within the Specialist Health Service in Norway» (link) (tick): ☒ Contact information: Name of the proposer (organization / institution / company / manufacturer): ViroGates A/S, Denmark Name of proposal contact: Jesper Eugen-Olsen, PhD Telephone number: +45 51 51 80 51 E-mail address: [email protected] Date and locality: 03-01-2019, Copenhagen Side 1 av 9 v4.0 11.12.2017 1. -
Utility of the Plasma Level of Supar in Monitoring Risk of Mortality During TB Treatment
Utility of the Plasma Level of suPAR in Monitoring Risk of Mortality during TB Treatment Paulo Rabna1, Andreas Andersen1, Christian Wejse1,2,3, Ines Oliveira4, Victor Francisco Gomes1, Maya Bonde Haaland3, Peter Aaby1,5, Jesper Eugen-Olsen1* 1 Bandim Health Project, Indepth Network, Bissau, Guinea-Bissau, 2 Department of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark, 3 Center of Global Health, School of Public Health, Aarhus University, Aarhus, Denmark, 4 Clinical Research Centre, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark, 5 Bandim Health Project, Statens Serum Institute, Copenhagen, Denmark Abstract Objective: To investigate whether changes in the plasma level of soluble urokinase plasminogen activator receptor (suPAR) can be used to monitor tuberculosis (TB) treatment efficacy. Design: This prospective cohort study included 278 patients diagnosed with active pulmonary TB and followed throughout the 8-month treatment period. Results: Mortality during treatment was higher in the highest inclusion quartile of suPAR (23%) compared to the lowest three quartiles (7%), the risk ratio being 3.1 (95% CI 1.65–6.07). No association between early smear conversion and subsequent mortality or inclusion suPAR was observed. After 1 and 2 months of treatment, an increase in suPAR compared to at diagnosis was associated with a Mortality Rate Ratio (MRR) of 4.5 (95%CI: 1.45–14.1) and 2.1 (95%CI 0.62–6.82), respectively, for the remaining treatment period. Conclusions: The present study confirmed that elevated suPAR level at time of initiation of TB treatment is associated with increased risk of mortality. Furthermore, increased suPAR levels after one month of treatment was associated with increased risk of mortality during the remaining 7-month treatment period. -
Virogates Has Been Granted a New Patent to Measure the Risk of Developing Life Style Related Diseases Using Its Suparnostic ® Biomarker Product
ViroGates has been granted a new patent to measure the risk of developing life style related diseases using its suPARnostic ® biomarker product Denmark, August 22, 2011 ViroGates, that develops and distributes the biomarker suPARnostic ®, today announced that it has been granted a patent in the UK, patent number GB2461410, based on the international patent application PCT/EP2007/064497. The patent is entitled “Method and tool for predicting cancer and other diseases”. The patent grant is the first related to the international patent application, and will allow ViroGates to pursue measuring and monitoring of patients’ blood, to determine whether the individual is at risk of developing life style related diseases such as cardiovascular diseases, type-2 diabetes (T2D), COPD and cancer. The grant of this patent further strengthens ViroGates’ patent portfolio, which comprises patents related to measuring and monitoring of various infectious diseases such as HIV, tuberculosis and various conditions of sepsis. The MONICA10 study (published in the Journal of Internal Medicine, 28 May 2010 by Jesper Eugen-Olsen, Ove Andersen and Steen B. Haugaard, Hvidovre University Hospital) has been the scientific basis for establishing this relation between suPAR and life style related diseases. The study documented that suPAR was predictive of development of cardiovascular diseases, diabetes and cancer, and particularly in predicting which individuals would progress to develop lung cancer. ViroGates, supported by a network of international key opinion leaders, is working towards establishing suPARnostic ® as a clinical decision-making product worldwide. “We are very excited to receive the news of this first grant of a patent relating to predicting serious life style related diseases” comments Jakob Knudsen, CEO of ViroGates. -
1 Instructions for Use Suparnostic® Turbilatex Reagents
1 Instructions for Use suPARnostic® TurbiLatex Reagents INTERPRETATION OF suPAR suPAR level Clinical decision soluble urokinase Plasminogen Activator Receptor <3 ng/mL Supports the decision of discharge. T005 The underlying health condition is good, and the prognosis for surviving is very high. suPARnostic® and the ViroGates A/S ViroGates logo are Banevaenget 13 3-6 ng/mL Some disease activity or co-morbidity is present. registered trademarks of Birkeroed 3460, Some readmissions and an elevated mortality are ViroGates A/S Denmark. Denmark expected after 6 months follow-up. ©2008 ViroGates. Tel: +45 2113 1336 www.virogates.com All rights reserved. >6 ng/mL Attention is needed. High risk of mortality. Further tests are needed to find the presence of severe disease. Table 1: Simplified suPAR clinical decision scheme (data from Danish hospital)3. Interpretation of results must be made considering the patient´s clinical history and results of other diagnostic tests. The decision to discharge This product is protected by one or more US, European, and/or foreign can, therefore, not be performed solely based on the patients suPAR patents. value. The T005 product is validated on the automated Roche Cobas c701/2 PRINCIPLES OF ASSAY PROCEDURE ® instrument (Cobas is a trademark of Roche), and this instruction for use The suPARnostic® TurbiLatex test is a turbidimetric immunoassay is dedicated for the Roche cobas c701/c702 biochemistry analyser. that quantitatively determines suPAR in human plasma samples. The first stage of testing is an incubation of human origin specimen (EDTA- Refer to the webpage http://www.virogates.com for instructions for use or Heparin plasma) with the R1 reagent. -
Novel Biomarkers in the Management of HPV-Positive & -Negative Oropharyngeal Carcinoma January 2016
THE UNIVERSITY OF SHEFFIELD Novel Biomarkers in the Management of HPV-Positive & -Negative Oropharyngeal Carcinoma Thesis submitted to the University of Sheffield for the degree of Doctor of Philosophy Robert Bolt Department of Oral & Maxillofacial Pathology January 2016 Abstract Human Papillomavirus (HPV)-related oropharyngeal carcinoma is considered to be in the early stages of an epidemic1-12. A marked rise in the incidence of this sexually-transmissible cancer has captured the public interest, and much debate exists over both the prophylactic and therapeutic strategies currently employed to manage this healthcare priority. HPV-positive oropharyngeal carcinoma is associated with highly favourable oncological outcomes. Clinical attention over recent years has been paid to the potential de-escalation of therapy in order to account for the disease’s favourable prognosis, in addition to reducing therapeutic burden in a well-prognosticating, younger patient cohort, for which consequences of radical chemo-radiotherapy strategies may disproportionately impact on longer-term quality of life. Whilst optimising the management of the ever-increasing proportion of HPV-positive oropharyngeal carcinomas is desirable and highly justifiable, it appears the poorer prognosticating HPV-negative oropharyngeal carcinoma has at least in part become overlooked. Oropharyngeal carcinoma is unique in comparison to many other established HPV-related cancers inasmuch as a clear HPV-negative subset exists, to which established aetiological factors (tobacco smoking and alcohol consumption) strongly correlate. For most other HPV- related carcinomas, such as cervical, anal and penile, tumours classified as HPV-negative are either regarded as potentially-virus containing, or else cannot be correlated to a definitive aetiological agent. Comparison of HPV-positive and -negative oropharyngeal carcinoma therefore offers unprecedented insight into the biological significance of each aetiological agent, and how prognostication of each disease may relate to tumour behaviour at a molecular level. -
See Virogates Presentation Here
ViroGates ViroGates A/S Västra Hamnen Investor Day 2 December 2020 ViroGates 2 ViroGates - a commercial stage company with approved products for the hospital sector ViroGates suPARnostic® products suPAR is the biomarker detected by ViroGates’ three CE-IVD marked suPARnostic® products and is a protein found in plasma. Description ViroGates A/S is an international medical technology ViroGates has established clinical utility of suPARnostic® supported by company developing and marketing blood test products +700 peer reviewed publications. under the suPARnostic® brand for better triaging in hospitals to: ViroGates has patented the clinical use of suPAR levels as a risk stratification method and currently holds 4 granted patent families and one newly filed application (2018). improve patient care reduce healthcare costs AUTO Flex ELISA Quick Triage TurbiLatex empower clinical staff Application R&D & clinical Near-patient Automated, use lab centralized lab ViroGates was founded in 2001 and has since 2018 been listed on Nasdaq First North Growth Market DK – Ticker Technology ELISA Lateral flow Turbidimetric “VIRO” Launch year 2009 2015 2018 (CE-IVD) ViroGates 3 suPAR is a marker of immune activation and a strong predictor disease severity and progession uPAR suPAR suPARnostic® +700 peer (soluble urokinase Plasminogen Activator Receptor) suPAR DI DI DII DII reviewed papers supporting A prognostic inflammatory DIII DIII evidence biomarker for immune activation indicating: Kidney disease Liver disease • Disease presence (acute, Diabetes Elevated -
Soluble Urokinase Plasminogen Activator Receptor Predicts
1112 Diabetes Care Volume 42, June 2019 Viktor Rotbain Curovic,1 Simone Theilade,1 Soluble Urokinase Plasminogen Signe A. Winther,1 Nete Tofte,1 Jesper Eugen-Olsen,2 Frederik Persson,1 Activator Receptor Predicts Tine W. Hansen,1 Jørgen Jeppesen,3,4 and Cardiovascular Events, Kidney Peter Rossing1,4 Function Decline, and Mortality in Patients With Type 1 Diabetes Diabetes Care 2019;42:1112–1119 | https://doi.org/10.2337/dc18-1427 OBJECTIVE Soluble urokinase plasminogen activator receptor (suPAR) is an important in- flammatory biomarker implicated in endothelial and podocyte dysfunction. How- ever, suPAR’s predictive qualities for complications in type 1 diabetes have yet to be determined. We investigated the prognostic value of suPAR for the development of cardiovascularevents,declineinrenalfunction, andmortalityinpatientswith type1 diabetes. RESEARCH DESIGN AND METHODS We included 667 patients with type 1 diabetes with various degrees of albuminuria inaprospective study. End points were cardiovascular events (cardiovascular death, nonfatal acute myocardial infarction, nonfatal stroke, or coronary or peripheral arterial interventions), estimated glomerular filtration rate (eGFR) decline ‡30%, progressionfromlowertohigheralbuminuricstate,developmentofend-stagerenal disease (ESRD), and mortality. Follow-up was 5.2–6.2 years. Results were adjusted for known risk factors. Hazard ratios (HRs) are presented per doubling of suPAR with 95% CI. Relative integrated discrimination improvement (rIDI) was calculated. 1Steno Diabetes Center Copenhagen, -
Plasma Levels of the Active Form of Supar Are Associated with COVID
Huang et al. Crit Care (2020) 24:704 https://doi.org/10.1186/s13054-020-03336-0 LETTER Open Access Plasma levels of the active form of suPAR are associated with COVID-19 severity Mingxiang Huang1†, Linlin Li2†, Jianshan Shen1, Yao Wang1, Rui Wang1, Cai Yuan3, Mingdong Huang2* and Longguang Jiang2,4* We read with great interest the recent study by Rovina not only signifcantly higher than those in healthy con- et al., who found that the elevation of soluble urokinase trols (p < 0.0001) but also slightly higher than those in plasminogen activator receptor (suPAR) plasma levels COVID-19 patients (p = 0.0278) (Table 1, Fig. 1a). Even in coronavirus disease 2019 (COVID-19) patients, and though more data needs to be collected and the back- suggested the suPAR can be an early predictor of severe ground of these patients are not clear, this is a signifcant respiratory failure [1]. Tere are three diferent suPAR research direction to pursue. If asymptomatic carriers forms (suPAR DI-III, suPAR DI, and suPAR DII-III) in could be identifed and quarantined in an early stage, it circulation, in which suPAR DI-III is defned as the active will prevent them from increasing the disease transmis- form of suPAR by its capability of binding to uPA [2]. In sion to an uncontrollable manner. addition, the uPA/uPAR system as a therapeutic target Patients involved three types of symptoms: moderate, has been proposed to reduce mortality of COVID-19 [3]; severe, and critical in our study (Table 1). Our data show therefore, further evaluation of the active form of suPAR that active suPAR levels increase as the disease worsens plasma levels in diferent symptom types of COVID-19 (Fig. -
Predicts Microalbuminuria in Patients at Risk for Type 2 Diabetes Mellitus
www.nature.com/scientificreports OPEN Soluble urokinase receptor (suPAR) predicts microalbuminuria in patients at risk for type 2 Received: 09 August 2016 Accepted: 08 December 2016 diabetes mellitus Published: 16 January 2017 Martina Guthoff1,2,3,*, Robert Wagner1,2,3,*, Elko Randrianarisoa1,2,3, Erifili Hatziagelaki4, Andreas Peter1,2,3, Hans-Ulrich Häring1,2,3, Andreas Fritsche1,2,3 & Nils Heyne1,2,3 Early identification of patients at risk of developing diabetic nephropathy is essential. Elevated serum concentrations of soluble urokinase receptor (suPAR) associate with diabetes mellitus and predict onset and loss of renal function in chronic kidney disease. We hypothesize, that suPAR may be an early risk indicator for diabetic nephropathy, preceding microalbuminuria. The relationship of baseline suPAR and incident microalbuminuria was assessed in a prospective long-term cohort of subjects at increased risk for type 2 diabetes (TULIP, n = 258). Association with albuminuria at later stages of disease was studied in a cross-sectional cohort with manifest type 2 diabetes (ICEPHA, n = 266). A higher baseline suPAR was associated with an increased risk of new-onset microalbuminuria in subjects at risk for type 2 diabetes (hazard ratio 5.3 (95% CI 1.1–25.2, p = 0.03) for the highest vs. lowest suPAR quartile). The proportion of subjects with prediabetes at the end of observation was higher in subjects with new-onset microalbuminuria. suPAR consistently correlated with albuminuria in a separate cohort with manifest type 2 diabetes. Elevated baseline suPAR concentrations independently associate with new-onset microalbuminuria in subjects at increased risk of developing type 2 diabetes. -
Virogates A/S Investor Presentation 16 June 2020 Danske Bank, Copenhagen Virogates
ViroGates ViroGates A/S Investor Presentation 16 June 2020 Danske Bank, Copenhagen ViroGates Forward-looking statements Certain information set forth and given in this presentation contains “forward-looking information”, including “future oriented financial information” and “financial outlook”, under applicable securities laws (collectively referred to herein as forward-looking statements). Except for statements of historical fact, information contained herein constitutes forward-looking statements and includes, but is not limited to, the (i) projected financial performance of ViroGates A/S (ViroGates); (ii) the expected development of ViroGates’ business, projects and joint ventures; (iii) execution of ViroGates’ vision and growth strategy, including with respect to future M&A activity and global growth; (iv) sources and availability of third-party financing for ViroGates’ projects; (v) completion of ViroGates’ projects that are currently underway, in development or otherwise under consideration; (vi) renewal of ViroGates’ current customer, supplier and other material agreements; and (vii) future liquidity, working capital, and capital requirements. Forward-looking statements are provided to allow potential investors the opportunity to understand management’s beliefs and opinions in respect of the future so that they may use such beliefs and opinions as one factor in evaluating an investment. These statements are not guarantees of future performance and undue reliance should not be placed on them. Such forward- looking statements necessarily -
Supar Level Is Associated with Myocardial Impairment Assessed
174:6 S Theilade and others suPAR associated with 174:6 745–753 Clinical Study myocardial impairment suPAR level is associated with myocardial impairment assessed with advanced echocardiography in patients with type 1 diabetes with normal ejection fraction and without known heart disease or end-stage renal disease Simone Theilade1, Peter Rossing1,2,3, Jesper Eugen-Olsen4, Jan S Jensen3,5 and Magnus T Jensen1,5,6 1 2 3 Steno Diabetes Center, Gentofte, Denmark, Aarhus University, Aarhus, Denmark, University of Copenhagen, Correspondence 4 Copenhagen, Denmark, Clinical Research Center, Hvidovre Hospital, Hvidovre, Denmark, should be addressed 5 6 Department of Cardiology, Gentofte Hospital, Gentofte, Denmark and Department of Internal Medicine, to S Theilade Holbaek Sygehus, Holbaek, Denmark Email [email protected] Abstract Aim: Heart disease is a common fatal diabetes-related complication. Early detection of patients at particular risk of heart disease is of prime importance. Soluble urokinase plasminogen activator receptor (suPAR) is a novel biomarker for development of cardiovascular disease. We investigate if suPAR is associated with early myocardial impairment assessed with advanced echocardiographic methods. Methods: In an observational study on 318 patients with type 1 diabetes without known heart disease and European Journal European of Endocrinology with normal left ventricular ejection fraction (LVEF) (biplane LVEF >45%), we performed conventional, tissue Doppler and speckle tracking echocardiography, and measured plasma suPAR levels. Associations between myocardial function and suPAR levels were studied in adjusted models including significant covariates. Results: Patients were 55 ± 12 years (mean ± S.D.) and 160 (50%) males. Median (interquartile range) suPAR was 3.4 (1.7) ng/mL and LVEF was 58 ± 5%.