Demand management
Demand management is being applied to this funding opportunity. Further details are provided in the ‘Who can apply’ section.
Scope
Funding is available for pre-clinical and early translational research on the development of medical countermeasures (MCMs) for chemical, biological, radiological and nuclear (CBRN) threats. Your project can start and finish at any stage on the developmental pathway from early prototype development, through pre-clinical refinement and testing, to early-phase clinical studies and trials (up to phase 2a).
Projects must generate evidence which contributes to improving domestic preparedness for CBRN incidents, particularly improving the health system’s preparedness. Examples include:
- the development of novel vaccines, diagnostics and therapeutics for CBRN threats
- broad-spectrum interventions for CBRN exposure
- symptomatic management approaches to treat CBRN exposure
- medicines repurposing studies, using existing therapies for the treatment of CBRN threats
Priority areas for research are:
- broad spectrum MCMs for threats that focus on treating shared symptomology or toxidrome
- drug repurposing studies to identify and evaluate suitable licensed drugs which may be held locally within hospitals and pharmacies
- novel vaccines, therapeutics and diagnostics for priority pathogens
- diagnostic and detection capabilities for radiological and nuclear incidents
Activities we do not support
This funding opportunity will not support:
- fundamental or investigative research not linked to a development plan, supported by the MRC science areas such as MRC: research grant: applicant-led
- studies where the main aim is to investigate disease mechanism (supported by the MRC Experimental Medicine Panel)
- technology development not aligned to a medical or clinical developmental plan, likely Biotechnology and Biological Sciences Research Council (BBSRC) or Engineering and Physical Sciences Research Council (EPSRC) remit
- studies investigating only the physiological response to CBRN agent exposure without a focus on medical countermeasures
- observational studies involving no experimental challenge
Duration
The duration of this award is a maximum of 30 months.
Award start date
Projects should start one to six months after the funding decision date.
Funding available
The FEC of your project can be up to a maximum of £4 million.
MRC will fund 80% of the FEC.
Find out more about full economic costing.
What we will fund
You can request funding for costs such as:
- a contribution to the salary of the project lead and co-leads
- support for other posts such as research and technical staff
- research consumables
- equipment
- travel costs
- data preservation, data sharing and dissemination costs
- estates and indirect costs
- public partnerships and related activities, including payments to public contributors
What we will not fund
We will not fund:
- costs for PhD studentships
- publication costs
- funding to use as a ‘bridge’ between grants
- costs associated with applying for IP protection, for example, patent filing
Collaborations
We encourage working with UK industry partners where these partnerships can add value to the project.
Collaborators may add value by giving access to:
- expertise
- technologies
- reagents
- funding
Please note that collaboration is not a prerequisite for application. You should make a clear case for the application being academic-led and requiring MRC funding to support the work proposed.
Be clear about any conflicts of interest and how they will be managed through the conflict of interest policies at the project lead’s research organisation.
Project partner
A project partner is a collaborating organisation in the UK, who will have an integral role in the proposed research. You may include team project partners that will support your research project through cash or in-kind contributions, such as:
- staff time
- access to equipment
- sites or facilities
- the provision of data
- software or materials
- recruitment of people as research participants
- providing samples, such as human tissue, for the project
Each project partner must provide a statement of support. If your application involves industry partners, they must provide additional information if the team project partner falls within the industry collaboration framework.
Find out more about subcontractors and dual roles.
Who cannot be included as a project partner
Any individual included in your application with a core team cannot also be a project partner.
Any organisation that employs a member of the application core team cannot be a project partner organisation, this includes other departments within the same organisation.
If you are collaborating with someone in your organisation, consider including them in the core team as project co-lead, or specialist. They cannot be a project partner.
Supporting skills and talent
We encourage you to follow the principles of the Concordat to Support the Career Development of Researchers and the Technician Commitment.
Trusted Research and Innovation (TR&I)
UK Research and Innovation (UKRI) is committed in ensuring that effective international collaboration in research and innovation takes place with integrity and within strong ethical frameworks. Trusted Research and Innovation (TR&I) is a UKRI work programme designed to help protect all those working in our thriving and collaborative international sector by enabling partnerships to be as open as possible, and as secure as necessary. Our TR&I Principles set out UKRI’s expectations of organisations funded by UKRI in relation to due diligence for international collaboration.
As such, applicants for UKRI funding may be asked to demonstrate how their proposed projects will comply with our approach and expectation towards TR&I, identifying potential risks and the relevant controls you will put in place to help proportionately reduce these risks.
See further guidance and information about TR&I, including where applicants can find additional support.