Skip to main content
Top
Published in: Trials 1/2019

Open Access 01-12-2019 | Methodology

Budgeting of non-commercial clinical trials: development of a budget tool by a public funding agency

Authors: Hilde Nevens, Jillian Harrison, France Vrijens, Leen Verleye, Nelle Stocquart, Elisabeth Marynen, Frank Hulstaert

Published in: Trials | Issue 1/2019

Login to get access

Abstract

Background

Investigator-led multicentre randomised trials are essential to generate evidence on the optimal use of medical interventions. These non-commercial trials are often hampered by underfunding, which may lead to difficulties in gathering a team with the necessary expertise, a delayed trial start, slow recruitment and even early trial discontinuation. As a new public funder of pragmatic clinical trials, the KCE Trials programme was committed to correctly pay all trial activities in order to assure timely delivery of high-quality trial results. As no appropriate trial budget tool was readily publicly available that took into account the costs for the sponsor as well as the costs for participating sites, we developed a tool to make the budgeting of a clinical trial efficient, transparent and fair across applicants.

Methods

All trial-related activities of the sponsor and sites were categorised, and cost drivers were identified. All elements were included in a spreadsheet tool allowing the sponsor team to calculate in detail the various activities of a clinical trial and to appreciate the budget impact of specific cost drivers, e.g. a delay in recruitment. Hourly fees by role were adapted from published data. Fixed amounts per activity were developed when appropriate.

Results

This publicly available tool has already been used for 17 trials funded since the start of the KCE Trials programme in 2016, and it continues to be used and improved. This budget tool is used together with additional risk-reducing measures such as a multistep selection process with advance payments, a recruitment feasibility check by sponsor and funder, a close monitoring of study progress and a milestone-based payment schedule with the last payment made when the manuscript is submitted.

Conclusions

The budget tool helps the KCE Trials programme to answer relevant research questions in a timely way, within budget and with high quality, a necessary condition to achieve impact of this programme for patients, clinical practice and healthcare payers.
Appendix
Available only for authorised users
Literature
1.
go back to reference Neyt M, Christiaens T, Demotes J, Hulstaert F. Publicly funded practice-oriented clinical trials. Brussels: Belgian Health Care Knowledge Centre (KCE); 2015. Neyt M, Christiaens T, Demotes J, Hulstaert F. Publicly funded practice-oriented clinical trials. Brussels: Belgian Health Care Knowledge Centre (KCE); 2015.
2.
go back to reference Viergever RF, Hendriks TC. The 10 largest public and philanthropic funders of health research in the world: what they fund and how they distribute their funds. Health Res Policy Syst. 2016;14:12.CrossRef Viergever RF, Hendriks TC. The 10 largest public and philanthropic funders of health research in the world: what they fund and how they distribute their funds. Health Res Policy Syst. 2016;14:12.CrossRef
3.
go back to reference Bertolini F, Sukhatme VP, Bouche G. Drug repurposing in oncology–patient and health systems opportunities. Nat Rev Clin Oncol. 2015;12(12):732–42.CrossRef Bertolini F, Sukhatme VP, Bouche G. Drug repurposing in oncology–patient and health systems opportunities. Nat Rev Clin Oncol. 2015;12(12):732–42.CrossRef
4.
go back to reference Naci H, Ioannidis JP. Comparative effectiveness of exercise and drug interventions on mortality outcomes: metaepidemiological study. BMJ. 2013;347:f5577.CrossRef Naci H, Ioannidis JP. Comparative effectiveness of exercise and drug interventions on mortality outcomes: metaepidemiological study. BMJ. 2013;347:f5577.CrossRef
5.
go back to reference Williams HC, Burden-Teh E, Nunn AJ. What is a pragmatic clinical trial? J Invest Dermatol. 2015;135(6):1–3.CrossRef Williams HC, Burden-Teh E, Nunn AJ. What is a pragmatic clinical trial? J Invest Dermatol. 2015;135(6):1–3.CrossRef
6.
go back to reference Anderson ML, Califf RM, Sugarman J, participants in the NIH Health Care Systems Research Collaboratory Cluster Randomized Trial Workshop. Ethical and regulatory issues of pragmatic cluster randomized trials in contemporary health systems. Clin Trials. 2015;12(3):276–86.CrossRef Anderson ML, Califf RM, Sugarman J, participants in the NIH Health Care Systems Research Collaboratory Cluster Randomized Trial Workshop. Ethical and regulatory issues of pragmatic cluster randomized trials in contemporary health systems. Clin Trials. 2015;12(3):276–86.CrossRef
7.
go back to reference Califf RM, Sugarman J. Exploring the ethical and regulatory issues in pragmatic clinical trials. Clin Trials. 2015;12(5):436–41.CrossRef Califf RM, Sugarman J. Exploring the ethical and regulatory issues in pragmatic clinical trials. Clin Trials. 2015;12(5):436–41.CrossRef
8.
go back to reference Pham CT, Karnon JD, Middleton PF, Bloomfield FH, Groom KM, Crowther CA, et al. Randomised clinical trials in perinatal health care: a cost-effective investment. Med J Aust. 2017;207(7):289–93.CrossRef Pham CT, Karnon JD, Middleton PF, Bloomfield FH, Groom KM, Crowther CA, et al. Randomised clinical trials in perinatal health care: a cost-effective investment. Med J Aust. 2017;207(7):289–93.CrossRef
9.
go back to reference Schilsky RL. Publicly funded clinical trials and the future of cancer care. Oncologist. 2013;18(2):232–8.CrossRef Schilsky RL. Publicly funded clinical trials and the future of cancer care. Oncologist. 2013;18(2):232–8.CrossRef
10.
go back to reference Mailankody S, Prasad V. Comparative effectiveness questions in oncology. N Engl J Med. 2014;370(16):1478–81.CrossRef Mailankody S, Prasad V. Comparative effectiveness questions in oncology. N Engl J Med. 2014;370(16):1478–81.CrossRef
11.
go back to reference Perner A, Haase N, Guttormsen AB, Tenhunen J, Klemenzson G, Aneman A, et al. Hydroxyethyl starch 130/0.42 versus Ringer’s acetate in severe sepsis. N Engl J Med. 2012;367(2):124–34.CrossRef Perner A, Haase N, Guttormsen AB, Tenhunen J, Klemenzson G, Aneman A, et al. Hydroxyethyl starch 130/0.42 versus Ringer’s acetate in severe sepsis. N Engl J Med. 2012;367(2):124–34.CrossRef
12.
go back to reference Unger JM, LeBlanc M, Blanke CD. The effect of positive SWOG treatment trials on survival of patients with cancer in the US population. JAMA Oncol. 2017;3(10):1345–51.CrossRef Unger JM, LeBlanc M, Blanke CD. The effect of positive SWOG treatment trials on survival of patients with cancer in the US population. JAMA Oncol. 2017;3(10):1345–51.CrossRef
13.
go back to reference Annemans L, Cleemput I, Hulstaert F, Simoens S. Comparative effectiveness research and measuring the level of pharmaceutical innovation in the EU. J Comp Eff Res. 2012;1(1):19–29.CrossRef Annemans L, Cleemput I, Hulstaert F, Simoens S. Comparative effectiveness research and measuring the level of pharmaceutical innovation in the EU. J Comp Eff Res. 2012;1(1):19–29.CrossRef
14.
go back to reference Walters SJ, Bonacho Dos Anjos Henriques-Cadby I, Bortolami O, Flight L, Hind D, Jacques RM, et al. Recruitment and retention of participants in randomised controlled trials: a review of trials funded and published by the United Kingdom Health Technology Assessment Programme. BMJ Open. 2017;7(3):e015276.CrossRef Walters SJ, Bonacho Dos Anjos Henriques-Cadby I, Bortolami O, Flight L, Hind D, Jacques RM, et al. Recruitment and retention of participants in randomised controlled trials: a review of trials funded and published by the United Kingdom Health Technology Assessment Programme. BMJ Open. 2017;7(3):e015276.CrossRef
19.
go back to reference van Asselt T, Ramaekers B, Corro Ramos I, Joore M, Al M, Lesman-Leegte I, et al. Research costs investigated: a study into the budgets of Dutch publicly funded drug-related research. Pharmacoeconomics. 2018;36(1):105–13.CrossRef van Asselt T, Ramaekers B, Corro Ramos I, Joore M, Al M, Lesman-Leegte I, et al. Research costs investigated: a study into the budgets of Dutch publicly funded drug-related research. Pharmacoeconomics. 2018;36(1):105–13.CrossRef
20.
go back to reference Büro für Technikfolgen-Abschätzung beim Deutschen Bundestag (TAB). Stand und Bedingungen klinischer Forschung in Deutschland und im Vergleich zu anderen Ländern unter besondere Berücksichtigung nichtkommerzieller Studien. Innovationsreport. Arbeitsbericht nr. 135; 2010. Büro für Technikfolgen-Abschätzung beim Deutschen Bundestag (TAB). Stand und Bedingungen klinischer Forschung in Deutschland und im Vergleich zu anderen Ländern unter besondere Berücksichtigung nichtkommerzieller Studien. Innovationsreport. Arbeitsbericht nr. 135; 2010.
21.
go back to reference Djurisic S, Rath A, Gaber S, Garattini S, Bertele V, Ngwabyt SN, et al. Barriers to the conduct of randomised clinical trials within all disease areas. Trials. 2017;18(1):360.CrossRef Djurisic S, Rath A, Gaber S, Garattini S, Bertele V, Ngwabyt SN, et al. Barriers to the conduct of randomised clinical trials within all disease areas. Trials. 2017;18(1):360.CrossRef
23.
go back to reference Cowie MR, Blomster JI, Curtis LH, Duclaux S, Ford I, Fritz F, et al. Electronic health records to facilitate clinical research. Clin Res Cardiol. 2017;106(1):1–9.CrossRef Cowie MR, Blomster JI, Curtis LH, Duclaux S, Ford I, Fritz F, et al. Electronic health records to facilitate clinical research. Clin Res Cardiol. 2017;106(1):1–9.CrossRef
24.
go back to reference Johnston SC, Rootenberg JD, Katrak S, Smith WS, Elkins JS. Effect of a US National Institutes of Health programme of clinical trials on public health and costs. Lancet. 2006;367(9519):1319–27.CrossRef Johnston SC, Rootenberg JD, Katrak S, Smith WS, Elkins JS. Effect of a US National Institutes of Health programme of clinical trials on public health and costs. Lancet. 2006;367(9519):1319–27.CrossRef
25.
go back to reference Martin L, Hutchens M, Hawkins C, Radnov A. How much do clinical trials cost? Nat Rev Drug Discov. 2017;16(6):381–2.CrossRef Martin L, Hutchens M, Hawkins C, Radnov A. How much do clinical trials cost? Nat Rev Drug Discov. 2017;16(6):381–2.CrossRef
27.
go back to reference Sertkaya A, Wong HH, Jessup A, Beleche T. Key cost drivers of pharmaceutical clinical trials in the United States. Clin Trials. 2016;13(2):117–26.CrossRef Sertkaya A, Wong HH, Jessup A, Beleche T. Key cost drivers of pharmaceutical clinical trials in the United States. Clin Trials. 2016;13(2):117–26.CrossRef
28.
go back to reference Speich B, von Niederhausern B, Blum CA, Keiser J, Schur N, Furst T, et al. Retrospective assessment of resource use and costs in two investigator-initiated randomized trials exemplified a comprehensive cost item list. J Clin Epidemiol. 2018;96:73–83.CrossRef Speich B, von Niederhausern B, Blum CA, Keiser J, Schur N, Furst T, et al. Retrospective assessment of resource use and costs in two investigator-initiated randomized trials exemplified a comprehensive cost item list. J Clin Epidemiol. 2018;96:73–83.CrossRef
29.
go back to reference Speich B, von Niederhausern B, Schur N, Hemkens LG, Furst T, Bhatnagar N, et al. Systematic review on costs and resource use of randomized clinical trials shows a lack of transparent and comprehensive data. J Clin Epidemiol. 2018;96:1–11.CrossRef Speich B, von Niederhausern B, Schur N, Hemkens LG, Furst T, Bhatnagar N, et al. Systematic review on costs and resource use of randomized clinical trials shows a lack of transparent and comprehensive data. J Clin Epidemiol. 2018;96:1–11.CrossRef
30.
go back to reference Speich B, Gloy V, Schur N, Ewald H, Hemkens LG, Schwenkglenks M, et al. A scoping review shows that several nonvalidated budget planning tools for randomized trials are available. J Clin Epidemiol. 2020;117:9–19.CrossRef Speich B, Gloy V, Schur N, Ewald H, Hemkens LG, Schwenkglenks M, et al. A scoping review shows that several nonvalidated budget planning tools for randomized trials are available. J Clin Epidemiol. 2020;117:9–19.CrossRef
31.
go back to reference Swartenbroekx N, Obyn C, Guillaume P, Lona M, Cleemput I. Manual for cost-based pricing of hospital interventions. Health Technology Assessment (HTA). Brussels: Belgian Health Care Knowledge Centre (KCE). KCE Report 178C.; 2012. Swartenbroekx N, Obyn C, Guillaume P, Lona M, Cleemput I. Manual for cost-based pricing of hospital interventions. Health Technology Assessment (HTA). Brussels: Belgian Health Care Knowledge Centre (KCE). KCE Report 178C.; 2012.
32.
go back to reference Hind D, Reeves BC, Bathers S, Bray C, Corkhill A, Hayward C, et al. Comparative costs and activity from a sample of UK clinical trials units. Trials. 2017;18(1):203.CrossRef Hind D, Reeves BC, Bathers S, Bray C, Corkhill A, Hayward C, et al. Comparative costs and activity from a sample of UK clinical trials units. Trials. 2017;18(1):203.CrossRef
33.
go back to reference Briel M, Olu KK, von Elm E, Kasenda B, Alturki R, Agarwal A, et al. A systematic review of discontinued trials suggested that most reasons for recruitment failure were preventable. J Clin Epidemiol. 2016;80:8–15.CrossRef Briel M, Olu KK, von Elm E, Kasenda B, Alturki R, Agarwal A, et al. A systematic review of discontinued trials suggested that most reasons for recruitment failure were preventable. J Clin Epidemiol. 2016;80:8–15.CrossRef
34.
go back to reference Lauer MS, D'Agostino RB Sr. The randomized registry trial—the next disruptive technology in clinical research? N Engl J Med. 2013;369(17):1579–81.CrossRef Lauer MS, D'Agostino RB Sr. The randomized registry trial—the next disruptive technology in clinical research? N Engl J Med. 2013;369(17):1579–81.CrossRef
35.
go back to reference Mathes T, Buehn S, Prengel P, Pieper D. Registry-based randomized controlled trials merged the strength of randomized controlled trials and observational studies and give rise to more pragmatic trials. J Clin Epidemiol. 2018;93:120–7.CrossRef Mathes T, Buehn S, Prengel P, Pieper D. Registry-based randomized controlled trials merged the strength of randomized controlled trials and observational studies and give rise to more pragmatic trials. J Clin Epidemiol. 2018;93:120–7.CrossRef
36.
go back to reference Jolly SS, Cairns JA, Yusuf S, Meeks B, Pogue J, Rokoss MJ, et al. Randomized trial of primary PCI with or without routine manual thrombectomy. N Engl J Med. 2015;372(15):1389–98.CrossRef Jolly SS, Cairns JA, Yusuf S, Meeks B, Pogue J, Rokoss MJ, et al. Randomized trial of primary PCI with or without routine manual thrombectomy. N Engl J Med. 2015;372(15):1389–98.CrossRef
37.
go back to reference Lagerqvist B, Frobert O, Olivecrona GK, Gudnason T, Maeng M, Alstrom P, et al. Outcomes 1 year after thrombus aspiration for myocardial infarction. N Engl J Med. 2014;371(12):1111–20.CrossRef Lagerqvist B, Frobert O, Olivecrona GK, Gudnason T, Maeng M, Alstrom P, et al. Outcomes 1 year after thrombus aspiration for myocardial infarction. N Engl J Med. 2014;371(12):1111–20.CrossRef
39.
go back to reference Sheffet AJ, Flaxman L, Tom M, Hughes SE, Longbottom ME, Howard VJ, et al. Financial management of a large multisite randomized clinical trial. Int J Stroke. 2014;9(6):811–3.CrossRef Sheffet AJ, Flaxman L, Tom M, Hughes SE, Longbottom ME, Howard VJ, et al. Financial management of a large multisite randomized clinical trial. Int J Stroke. 2014;9(6):811–3.CrossRef
Metadata
Title
Budgeting of non-commercial clinical trials: development of a budget tool by a public funding agency
Authors
Hilde Nevens
Jillian Harrison
France Vrijens
Leen Verleye
Nelle Stocquart
Elisabeth Marynen
Frank Hulstaert
Publication date
01-12-2019
Publisher
BioMed Central
Published in
Trials / Issue 1/2019
Electronic ISSN: 1745-6215
DOI
https://doi.org/10.1186/s13063-019-3900-8

Other articles of this Issue 1/2019

Trials 1/2019 Go to the issue