Independence of research
This strategy outlines how our research is funded and how independence from industry funding is maintained. It also covers the department's policy on consultancies, honoraria or other personal benefits.
Oxford Population Health (the Nuffield Department of Population Health) is a medical research and teaching department within the University of Oxford’s Medical Sciences Division, with a focus on the causes, prevention and treatment of premature death and disability worldwide. It employs around 600 people, including clinicians, statisticians, social scientists, other researchers, IT and other research support staff. Many of its scientists are world-leading experts in their field and collaborate extensively with other researchers around the world.
Research at Oxford Population Health is funded in a number of ways. Much of the funding is peer-reviewed, which involves other experts independently assessing the Department’s planned research. Such support is provided by a number of government institutions and charities, including the Medical Research Council, National Institute for Health and Care Research, Department of Health and Social Care, British Heart Foundation, Cancer Research UK and Wellcome. In addition, funding is obtained from healthcare companies, particularly for large studies of the treatment and prevention of disease. The department's research is conducted independently of the funding sources.
After completion of Oxford Population Health's studies, reports of their results are written (without restrictions by the funders) and submitted to general or specialist journals, where they typically undergo peer-review before publication. Oxford Population Health staff publish nearly 1000 papers per year. Every five years or so, an assessment of University-based research that is used to determine the distribution of government research funding to universities is undertaken. The most recent assessment in 2021 found that 96% of the research submitted with research from the Nuffield Department of Primary Care Health Sciences was ranked either 4* (world-leading in terms of originality, significance and rigour) or 3* (internationally excellent in terms of originality, significance and rigour).
Oxford Population Health aims to address important health questions which can sometimes require very large studies to produce reliable findings. In the case of common life-threatening illnesses (such as heart disease, stroke and cancer), even small advances in prevention and treatment can help to avoid thousands of premature deaths and much disability worldwide.
The conduct of clinical trials that involve many thousands of participants, often in multiple countries around the world, requires a substantial research effort and can be very expensive. Given the costs involved, industry funding and provision of study drugs help to ensure that clinical trials can be of sufficient size and scope to assess the safety and efficacy of treatments reliably. Likewise, large-scale observational studies of the associations of risk factors with disease may well require substantial investment in genetic and other assays by industry in order to unlock scientifically important data for population health research.
Oxford Population Health staff decide what studies in which to be involved for scientific reasons and then seek government, charity and/or industry research funding to cover the costs. For example, the department's researchers have taken a lead in clarifying the relevance of cholesterol to the risk of cardiovascular disease, and then assessing the impact of lowering cholesterol levels with statin therapy. In the case of the Heart Protection Study, it took several years to obtain the funding, with half coming from the Medical Research Council (government) and the British Heart Foundation (charity), one quarter from Merck (manufacturer of simvastatin) and one quarter from Roche (manufacturer of vitamins E, C and beta-carotene). That trial showed statin therapy reduces the risk of heart attacks and strokes safely for a wide range of patients at high risk of such events, but the vitamins produced no benefit. Both results were reported prominently by researchers independently of all of the funders.
All of the department's research that receives industry funding is governed by University of Oxford contracts which protect the independence of study design, conduct, analysis, interpretation and reporting. Oxford Population Health (not the funders) controls the databases, and controls the analyses and interpretation of its studies, with no restrictions from funders on what is reported.
The department does not engage in activities that pose or appear to pose a conflict of interest. In particular, Oxford Population Health would not accept funding for research from tobacco or alcohol companies, and has carefully limited engagement with food and nutrition companies.
Acceptance of Honoraria Payments and Participation in Industry Meetings
Honoraria are payments made for activities notionally provided without charge. Staff may accept honoraria payments, but care should be taken to ensure that the source of the funding does not raise conflict of interest issues. (For example, funding from a potentially conflicted source may be made to appear legitimate by channeling it through a University.)
Oxford Population Health has an explicit policy of not accepting any personal honoraria payments directly or indirectly from the pharmaceutical and food industries. It only seeks reimbursement to the University of Oxford for the costs of travel and accommodation to participate in scientific meetings. This approach is intended to help ensure that decisions to give lectures or advice are determined by the scientific value of doing so, and not by personal financial gain.
Invitations from pharmaceutical or food companies to participate in meetings should be considered carefully to ensure they are scientifically legitimate, or that a specific scientific interest of the department would be served by acceptance. If not, such invitations should be declined.
Consultancy agreements
The University’s view is that consultancy can be an important means by which staff make their knowledge and expertise available to government, public sector organisations, community groups and business. Any consultancy activity by staff must be approved by both the Head of Group and the Head of Department. It must fulfil the following criteria:
- The purpose of the consultancy should be clearly stated.
- It should not pose or appear to cause a conflict of interest.
- No payments directly or indirectly from pharmaceutical or food companies.
- It should be limited to provision of advice and assistance, and not include undertaking of substantial research for external bodies (which should be funded by a research grant).
Anyone considering any paid activity outside the department should first discuss it with their line manager and Head of Group. In addition, any external activities leading to consultancies, should be reviewed by Oxford University Consulting, which will carry out due diligence checks to ensure compliance with relevant University ethics and funding policies.
Please see the relevant University guidance on outside appointments, including consultancy agreements.
Investments
It is recognised that pensions are based on investments in companies over which staff have no control. However, it is recommended that staff do not hold shares directly in tobacco companies, or in pharmaceutical, biotechnology or food companies that might be affected by research or publications in which they are involved or by their public statements.
If in doubt about any of these issues, staff are encouraged to discuss these with their line manager or with members of the department’s HR team.
Commercial funding received by the Nuffield Department of Population Health, University of Oxford
|
Project Name |
Sponsor |
From |
To |
Award |
Additional info |
|
3-C trial of transplant rejection |
Novartis Pharmaceuticals UK Ltd |
2009 |
2017 |
350 |
|
|
A multicenter international randomized double-blind placebo-controlled clinical trial of the aldosterone synthase inhibitor BI 690517 in patients with chronic kidney disease treated with empagliflozin |
Boehringer Ingelheim International GmbH |
2023 |
2032 |
216,237 |
|
|
ACE trial of acarbose |
Bayer Plc |
2008 |
2022 |
135 |
* |
|
Africa Oxford (AfOx) Catalyst Grant |
Mastercard |
2022 |
1905 |
10 |
* |
|
An observational study of a multi-cancer early detection test (MCED) in individuals presenting with signs and symptoms of cancer in England |
GRAIL Bio UK Ltd |
2021 |
2026 |
70 |
* |
|
ASCEND PLUS |
Novo Nordisk A/S |
2021 |
2029 |
3,000 |
Plus drug supply |
|
ASCEND PLUS: A Study of Cardiovascular Events iN Diabetes |
Novo Nordisk A/S |
2021 |
2029 |
36,432 |
Plus drug supply |
|
ASCEND trial of aspirin and fish oils |
Bayer HealthCare LLC - USA |
2004 |
2013 |
53 |
Plus drug supply |
|
ASCEND trial of aspirin and fish oils |
Bayer AG |
2004 |
2017 |
1,826 |
|
|
ASCEND trial of aspirin and fish oils |
Solvay Pharmaceuticals GmbH |
2004 |
2013 |
584 |
|
|
ASCEND trial of aspirin and fish oils |
Abbott Product Operations AG |
2004 |
2017 |
1,532 |
|
|
Assessing the potential for SenseCam to fight the current global health crises of increasing obesity and physical inactivity |
Microsoft Research Ltd |
2010 |
2013 |
69 |
|
|
ATLAS trial of tamoxifen duration |
AstraZeneca UK Ltd |
2001 |
2018 |
508 |
|
|
BDI-Novartis Collaboration for AI in Medicine |
Novartis Pharma AG Switzerland |
2018 |
2027 |
404 |
* |
|
BEST-D pilot trial of vitamin D |
Tishcon |
2012 |
2014 |
0 |
Drug supply only |
|
BREXOME - rare variants in breast cancer |
Regeneron Pharmaceuticals Inc |
2020 |
2026 |
107 |
|
|
Burden of Antimicrobial Resistance and Antibiotic Treatment Failure in Low-, Middle- and High-Income Countries (BALANCE) & Burden of antibiotic resistance in neonates from developing societies (BARNARDS) II |
Ineos Group Limited |
2021 |
2031 |
144 |
* |
|
Can wearables improve the prediction of all-cause mortality, cardiovascular disease, and cancer in UK Biobank? |
Swiss Re Ltd |
2022 |
2026 |
645 |
|
|
Characterize the carriers of predicted loss-of –function variants in chymase |
Bayer AG |
2019 |
2021 |
297 |
|
|
Chinese case Control Study |
AstraZeneca AB |
2004 |
2015 |
154 |
Plus drug supply |
|
Development and validation of technology enabled, quantitative and sensitive measures of functional decline in people with early stage Alzheimer’s Disease. |
Janssen Pharmaceutica NV |
2022 |
2023 |
85 |
|
|
Development of Digital Biomarkers for Dementia |
Roche Diagnostics International AG |
2016 |
2022 |
477 |
|
|
Development of Digital Biomarkers for Dementia. |
Eli Lilly and Company USA |
2016 |
2022 |
600 |
|
|
Device-measured physical activity in EMPA-ASi HFpEF trial |
Boehringer Ingelheim International GmbH |
2024 |
2028 |
378 |
|
|
Device-measured physical activity in EMPA-ASi HFrEF trial |
Boehringer Ingelheim International GmbH |
2025 |
2029 |
489 |
|
|
Diabetic Peripheral Neuropathy Treatment with Dorsal Root Ganglion Stimulation a Randomised Controlled Trial |
St Jude Medical Europe Inc |
2018 |
2020 |
52 |
* |
|
DNA EXTRACTION AND GENOTYPING IN CKB |
GSK Research & Development Ltd |
2011 |
2015 |
2,465 |
|
|
DOCTOR REFERRAL OF OVERWEIGHT PEOPLE TO LOW ENERGY TREATMENTS |
Cambridge World Heritage Centre Ltd |
2015 |
2020 |
35 |
* |
|
DYNAMIC CONSENT USCF |
Oxford University Innovation Ltd |
2015 |
2017 |
28 |
|
|
Economic Analysis ofExenatide Versus Placebo in Patients with Type 2 Diabetes and Inadequate Glycemic Control with Diet Alone, or Therapy with one, two or three Oral An tihyperglycemic Agents (EXSCEL) |
Amylin Pharmaceuticals Inc |
2009 |
2022 |
473 |
* |
|
Elinogrel feasibility trial |
Novartis |
2010 |
2011 |
500 |
|
|
Estimating acceptable non-inferiority margins for antibioti stewardship interventions using discrete choice experiments |
Mars Petcare UK |
2021 |
2024 |
25 |
|
|
FOXFIRE trial of chemotherapy with or without radioembolisation for bowel cancer that has spread to the liver |
Sirtex Technology Pty Ltd |
2009 |
2017 |
228 |
* |
|
FUWAI RESEARCH FACILITY |
Merck Sharp & Dohme LLC |
2010 |
2024 |
1,111 |
|
|
Heart Protection Study follow-up studies |
Merck: £1.2M; GlaxoSmithKline: $400K; Liposcience: £50K |
2003 |
2010 |
1,650 |
|
|
HPS 4/TIMI 65 - ORION-4. |
Novartis Pharmaceuticals Corporation |
2017 |
2030 |
85,399 |
|
|
HPS2 |
Merck & Co Inc |
2005 |
2015 |
52,196 |
|
|
Investigation of proteomics in the China Kadoorie Biobank |
Novo Nordisk Ltd |
2021 |
2022 |
341 |
|
|
IRIS Initiative Phase II - Genome sequencing |
Merck Sharp & Dohme (UK) Ltd |
2023 |
2027 |
856 |
|
|
Large-scale multi-omics assays in China Kadoorie Biobank |
Bayer AG |
2020 |
2025 |
1,577 |
|
|
LENS trial in Non-proliferative retinopathy in Scotland |
Mylan: free drug supply only |
2016 |
2022 |
0 |
Drug supply only |
|
Leveraging Large Scale Biobanks to Investigate Digital Biomarkers for the Early Identification of Chronic Obstructive Pulmonary Disease |
GSK Research & Development Ltd |
2025 |
2028 |
681 |
|
|
MaatHRI Project (Ultromics) |
Ultromics Limited |
2018 |
2022 |
79 |
|
|
Measuring sleep characteristics using machine learning in wearable datasets. |
Novo Nordisk A/S |
2020 |
(blank) |
135 |
|
|
Mexico City Prospective Study - Amended and Restated Research Collaboration Agreement (Regeneron) |
Regeneron Pharmaceuticals Inc |
2021 |
2029 |
1,780 |
|
|
Mexico City Prospective Study - Amended and Restated Research Collaboration Agreement (Astrazeneca) |
AstraZeneca UK Ltd |
2021 |
2029 |
1,809 |
|
|
NAVIGATOR - HEALTH ECONOMICS PAPER |
Novartis Pharmaceuticals Corporation |
2013 |
2014 |
15 |
* |
|
Next generation sequencing analysis - a clinical study |
Life Technologies Corporation |
2011 |
2014 |
125 |
* |
|
NN-BDI Partnership: Integration of medical imaging and genetic data using machine learning for identification of micro and macro vascular disease targets |
Novo Nordisk A/S |
2021 |
2026 |
1,154 |
* |
|
NN-Big Data Partnership: Using data from wearable devices to identify novel targets for cardiometabolic disease (obesity, T2DM, NAFLD, & heart failure) |
Novo Nordisk A/S |
2021 |
2025 |
1,052 |
* |
|
Non invasive rapid assessment of liver disease using magnetic resonance |
Perspectum Ltd |
2016 |
2019 |
273 |
* |
|
Novartis EPSRC Centre for Doctoral Training in Healthcare Data Science DPhil Studentship |
Novartis Pharma AG Switzerland |
2024 |
2028 |
160 |
|
|
Novo Nordisk Fellowship Programme Renewal |
Novo Nordisk A/S |
2021 |
2034 |
460 |
* |
|
Novo-Nordisk Postdoctoral Fellowship Programme |
Novo Nordisk A/S |
2013 |
2025 |
217 |
* |
|
ORION-17 |
Novartis Pharma AG Switzerland |
2020 |
2023 |
1,059 |
|
|
Oxford-GSK Institute of Molecular & Computational Medicine |
GSK Research & Development Ltd |
2021 |
2028 |
263 |
* |
|
Oxford-GSK Study of COPD Using CKB Data |
GSK Research & Development Ltd |
2012 |
2015 |
1,110 |
|
|
Oxford-Janssen Human Genomics Fellowship Programme |
Janssen Biotech |
2020 |
2025 |
30 |
|
|
OxPod - Podium Institute |
Podium Analytics |
2021 |
2027 |
31 |
* |
|
Pharmacogenomic analysis of the Heart Protection Study using a CAD polygenic risk score |
Regeneron Pharmaceuticals Inc |
2020 |
2026 |
143 |
|
|
PROCARDIS genetic study |
AstraZeneca: £1.7M |
1998 |
2011 |
1,700 |
|
|
Randomized EValuation of the Effects of Anacetrapib through Lipid-modification (REVEAL) |
Merck Sharp & Dohme LLC |
2010 |
2022 |
108,110 |
|
|
Second Heart Protection Study (SEARCH) |
Merck & Co Inc |
1997 |
2009 |
22,727 |
Plus drug supply |
|
SHARP |
Merck & Co Inc |
2001 |
2017 |
39,617 |
Plus drug supply |
|
SHARP 3 |
Boehringer Ingelheim International GmbH |
2022 |
2023 |
1,809 |
|
|
SHARP-2 EMPRESS. |
Boehringer Ingelheim International GmbH |
2017 |
2029 |
106,252 |
|
|
Small open reading frames in drug discovery: from genetics to mechanisms to new therapies |
Novo Nordisk A/S |
2022 |
2026 |
48 |
* |
|
STICS (STATIN THERAPY IN CARDIAC SURGERY) ASTRAZENECA GRANT |
AstraZeneca UK Ltd |
2011 |
2016 |
61 |
|
|
TECOS Trial Evaluating Cardiovascular Outcomes with Sitagliptin |
Merck & Co Inc |
2008 |
2023 |
140 |
* |
|
The 3C Study - CAMPATH |
John Wyeth & Brother Limited |
2009 |
2017 |
530 |
|
|
THE ECONOMIC BURDEN OF MALIGNANT NEOPLASMS IN THE EU |
Pfizer Ltd |
2011 |
2012 |
37 |
|
|
The Oxford Participation & Activities Questionnaire (Ox-PAQ): Phase 2 Study Protocol - Actelion unrestricted grant |
Actelion Pharmaceuticals Ltd |
2015 |
2016 |
58 |
|
|
The Oxford-Novartis Collaboration for AI in Medicine |
Novartis Pharma AG Switzerland |
2024 |
2027 |
322 |
* |
|
Therapies for Influenza |
Oxon Epidemiology Limited |
2019 |
2023 |
77 |
|
|
Thrombotic Microangiopathy associated Pregnancy Acute Kidney Injury in the United Kingdom: Incidence, Outcomes and Risk Factors |
Alexion Pharmaceuticals Inc. |
2021 |
2022 |
32 |
|
|
UK HEART AND RENAL PROTECTION (UK-HARP)-III: LCZ696 IN PATIENTS WITH CHRONIC KIDNEY DISEASE: A PILOT STUDY |
Novartis Pharma AG Switzerland |
2013 |
2018 |
2,574 |
|
|
USING HUMAN GENETICS TO VALIDATE THERAPEUTIC TARGETS RELATED TO CLINICAL MEASURES AND RISK FOR CARDIOVASCULAR EVENTS |
Merck Sharp & Dohme LLC |
2012 |
2014 |
214 |
|
|
Using Whole Genome Sequencing Datasets to Identify Novel Disease Genes and Mechanisms. |
GSK Research & Development Ltd |
2020 |
2024 |
317 |
* |
Updated on 19-May-26
* Funds received by Nuffield Department of Population Health for collaborative research projects led by other Institutions or Oxford University departments
