Treatments and Adherence to Treatment protocols

Home Funding Calls for proposals Treatments and Adherence to Treatment protocols Treatments and Adherence to Treatment protocols OHAMR Grant Cascade funding Internal navigation General information Submission & evaluation process Further information Task description General Information Opening date 18 November 2025 Deadline model multiple cut-off Deadline dates 02 February 2026 13:00 (Brussels time) 17 June 2026 13:00 (Brussels time) Open For Submission Expected duration of participation The maximum duration of the project is three years Total funding available 31 000 000,00 € Project acronym OHAMR Full name of the EU funded project European Partnership One Health AntiMicrobial Resistance Grant agreement number 101217154 Topic HORIZON-HLTH-2024-DISEASE-09-01 - European Partnership: One Health Anti-Microbial Resistance Submission & evaluation process Call Topics: Research & innovation proposals submitted under the EUP OHAMR 2026 Joint Transnational Call must address one of the following topics: -Topic 1: Identify and develop new combination treatments using existing or innovative antimicrobials or antimicrobial with adjunctive treatments to extend drug efficacy and combat resistance. Resistance limits the usability of many commonly-used antibiotics and antifungal agents in Human Health, Animal Health, and Plant Health. Proposals addressing this topic should identify and develop therapies to be used in combination (combination of different antimicrobials, or combination of an antimicrobial and a non-antimicrobial that improves activity or facilitates a better targeting towards the site of infection) to reduce the development of resistance against antibacterial and antifungal treatments and extend the usability of inexpensive and readily available antimicrobials. These studies should be underpinned by scientific rationale and mechanism of action of these treatments. In the framework of this topic, improvement of existing combination treatments is eligible (i.e. pharmacokinetics and pharmacodynamics, mode of administration). The choice of the targeted pathogens should be well justified. For the proposals having a Human Health interest, the proposed combination treatment should be directed against one of the bacterial or fungal pathogens included in the WHO priority lists. -Topic 2: Develop tools and methods to improve adherence to treatment protocols. A low adherence to the treatment protocols by end-users (patients, farmers, citizens) leads to a decreased probability of success and to an increased risk of resistance to antibacterial and antifungal treatments. Proposals addressing this topic should identify the reasons of poor adherence to treatment protocols (Human, Animal, Plant), and/or develop innovative tools (including digital tools) and methods (including sociological and behavioural approaches) to improve the adherence to treatment protocols and/or test and compare the efficiency of existing or innovative tools and methods on the adherence to treatment protocols. Engagement with end-users is mandatory. The consideration of vulnerable groups, which often have reduced access to conventional health and care services, is expected. - Topic 3: Assess the impact of antimicrobials for veterinary and agricultural use on the risk of AMR transmission to humans and the environment to inform policies on the restriction of some antimicrobials for human use. Proposals addressing this topic are expected to assess the impact of mechanisms of action, formulations, routes of administration and treatment regimens of antibacterial and antifungal drugs authorized for veterinary and agricultural use on the risk of emergence and transmission of AMR to humans and the environment. Proposals addressing this topic should also aim to improve the formulation, dosage, delivery, routes of administration and treatment regimens (including pharmacokinetics and pharmacodynamics) currently used in the veterinary and agricultural sector, to decrease the risk of cross-resistance, or transmission to humans and the environment. The aim is to generate evidence to support policies that restrict certain antimicrobials for exclusive human use and inform policies such as the WHO List of Medically Important Antimicrobials. Submission procedures: -The call will only support transnational research and innovation projects (more details on the composition of the consortium and on the participating funding organisations can be found on the EUP OHAMR Website-https://ohamr.eu/) -The call will follow a two-step evaluation process (submission of a pre-proposal; successful consortia will be invited to submit a full proposal). -Pre-proposals and full proposals must be written in English, and must follow the format and the guidelines provided in the pre-/full proposal template. Pre-proposals or full proposals that do not follow the template guidelines (i.e. length of the different sections, number of CVs and letters of intent) will be rejected without further review. The pre-proposal template can be found on the EUP OHAMR website. The full proposal template will be sent to the project coordinators invited to the next evaluation stage. -Pre-proposals and full proposals must be submitted by the project coordinator on the EUP OHAMR on-line submission platform (https://ptoutline.eu/app/OHAMR2026_OH-TREAT). No other means of submission (i.e. post or e-mail) will be accepted. Please note that some funding organisations might request an additional mandatory submission on their own national/regional platform (see Annex A). Pre-/full proposals submitted on a national/regional platform but not on the EUP OHAMR submission platform will be rejected without further review. -Submission of pre-proposals or full proposals after the submission timeline will not be accepted. -All questions related to the general eligibility rules and general evaluation process should be addressed to the EUP OHAMR Joint Call Secretariat (JCS) (EUPOHAMR_calls@agencerecherche.fr). All questions related to the national/regional eligibility rules and national/regional eligibility costs should be addressed to the national/ regional funding organisations. -The only official communication line between the project consortia and the JCS is the project coordinator. Throughout the application procedure the JCS will only contact by e-mail the project coordinators, who must forward all information to other partners of their consortia. This includes evaluation results. Evaluation: Formal check and evaluation of pre-proposals The JCS will check all proposals to ensure that they meet the call’s formal criteria (i.e. date of submission; number and category of participating countries; inclusion of all necessary information in English; appropriate limits on length; signature of the letters of intent). In parallel, the JCS will forward the proposals to the national/regional funding organisations, which will perform a check for compliance with national/regional regulations. Each proposal passing both eligibility checks will be evaluated independently by three reviewers for a first evaluation (see evaluation criteria below). Potential conflicts of interests of the evaluators will be taken into consideration during the allocation of the proposals. The reviewers will perform the assessment of the pre-proposals and complete a written evaluation form with scores and comments for each evaluation criterion. During a Peer Review Panel (PRP) meeting, the reviewers will discuss all proposals and agree on a consensus score for each proposal. The outcome of the PRP will consist of 3 ranking lists (one ranking list for each topic). To avoid conflicts of interest, evaluators with a conflict related to a specific proposal (i.e. co-publication with one of the applicants during the last 5 years, current collaboration with one of the applicants, same research centre as one of the applicants, personal or professional links with one of the applicants that may compromises the evaluator impartiality, involvement in the preparation of the proposal) will not participate in the discussion of that proposal. The board of funders will meet to decide which proposals will be invited to submit a full proposal based on the reviewers’ recommendations and to ensure a reasonable balance of requested and available national/regional budgets. Pre-proposals which do not pass this assessment will not be invited for the full proposal stage. The consortia will receive a summary review report without scores written by one of the experts in charge of evaluating the proposal. Formal check and evaluation of full proposals The JCS will check the full proposals to ensure that they meet the call’s formal criteria and have not changed substantially from the respective pre-proposals (e.g. composition of the consortium, the objectives of the project or the requested budget). In parallel, the JCS will forward the proposals to the national/regional funding organisations, which will perform a check for compliance with national/regional regulations. Each full proposal passing both checks will be allocated to three reviewers taking the potential conflicts of interest into consideration. The reviewers will perform the assessment of the full proposal and complete a written evaluation form with scores and comments for each criterion (see evaluation criteria below). During a second PRP meeting, the reviewers will discuss all proposals and produce 3 ranking lists of proposals recommended for funding (one ranking list for each call topic). To avoid conflicts of interest, evaluators with a conflict related to a specific proposal will not participate in the discussion of that proposal. The final summary review report prepared by the evaluators will be sent to the respective project coordinators. Ethics and legal requirements Please note that at the full proposal stage, applicants will be required to complete a self-assessment checklist for ethics and to provide details on safety, animal studies, genetically modified organisms and microorganisms, environmental hazards and waste handling, data management, statistical methods, ethics and legal issues. Applicants should anticipate this requirement and ensure that they have consulted with relevant experts to verify the feasibility of the project, and that the proposal can be completed within the defined budget and within the prescribed time window. Full proposals recommended for funding by the PRP and selected for funding by the board of funders will undergo an ethics review by an Ethics Panel. Ethics experts will remotely check the selected proposal for their compliance with ethical norms and regulations. A meeting will also be organised for a discussion between the various ethics experts. If necessary, the ethics experts may ask the consortium for clarifications. The Ethics experts may highlight some vigilance points that need to be monitored during the implementation of the funded project. Only those proposals approved by both the scientific evaluation and ethics assessment (complying with all central Horizon Europe and regional/national ethical requirements) will be funded. Decision The funders will take their funding decision, based on the ranking lists established by the PRP, the available funding and the Ethics panel recommendations. The JCS will send by e-mail the funding recommendation to the project coordinator, who is then responsible to communicate this information to the respective project partners. Redress Procedure Applicants can appeal against the evaluation outcome if they suspect a breach in the implementation of the evaluation and selection procedures. This redress procedure only covers the procedural aspects of the evaluation. A mere disagreement with peer reviewers or panel members’ comments are not grounds for an appeal. The redress procedure will not call into question the scientific or technical judgement of appropriately qualified experts. The applicants shall submit their a [... συνέχεια στην επίσημη πρόσκληση]