HORIZON-MISS-2026-02-CANCER-03

Pragmatic clinical trials to optimise immunotherapeutic interventions for patients with refractory cancers

Status
open for submission
Programme
Horizon Europe (HORIZON)
Action type
HORIZON Research and Innovation Actions
Opens
10 Feb 2026
Deadline
15 Sep 2026
Fetched
15 Jul 2026, 07:18 UTC
Plain-language summary

Fund pragmatic clinical trials to optimize affordable immunotherapy for refractory cancer patients across Europe.

This call supports clinical trials to improve immunotherapy treatments for patients with refractory cancers. Trials should reflect real-world healthcare settings and focus on patient quality of life and survival. The goal is to provide evidence for affordable, tailored treatments accessible across European healthcare systems.

Likely relevant for

  • Clinical researchers in oncology
  • Immunotherapy specialists
  • Healthcare providers in oncology
  • Academic institutions conducting clinical trials
  • Health policy makers
  • Patient advocacy groups

Project signals

Focus on real-world effectiveness of immunotherapiesEndpoints including overall survival and patient-reported outcomesData disaggregated by sex, gender, age, socio-economic status, ethnicityInclusion of diverse European regions and healthcare settingsNetworking within EU Cancer Mission clusters

What it funds

  • Randomised or cluster-randomised pragmatic clinical trials for immunotherapeutic interventions in refractory cancers
  • Trials addressing any cancer subtype, disease stage, age group, or societal segment
  • Tailored, affordable immunotherapy adapted to local, regional, or national healthcare settings
  • Data collection disaggregated by sex, gender, age, socio-economic status, ethnicity
  • Support translational research limited to biomarker-informed patient stratification and trial analyses
  • Networking and collaboration activities within the EU Cancer Mission 'Diagnosis and Treatment' cluster

Expected outcomes

  • Improved access to optimized, affordable immunotherapies for refractory cancer patients and caregivers across Europe
  • Clinical evidence for healthcare professionals to deploy effective, evidence-based immunotherapy treatments
  • Support for healthcare providers and policymakers to implement and reimburse optimized immunotherapies in routine practice

Who can apply / participate

  • Academic institutions
  • Healthcare providers
  • Research organisations
  • Small and medium-sized enterprises (SMEs)
  • Patient organisations and representatives
  • Public authorities and health authorities
  • Proposals should include a mix of stakeholders from various disciplines and sectors
  • Involvement of regional and national health authorities is required
  • Collaboration across European regions, EU Member States, and Associated Countries is expected
  • Eligible participants from EU Member States and Associated Countries
  • Check eligibility of non-EU/non-Associated countries according to Horizon Europe rules
  • Proposals must be investigator-initiated pragmatic clinical trials
  • Trials must be independent from commercial interests and focus on public health benefits
  • Data must be disaggregated by relevant demographic and socio-economic variables
  • Specific eligibility criteria for certain participant types
  • Exact consortium size and composition requirements

Must check before shortlisting

  • Eligibility of applicant types and countries
  • Budget and lump sum funding conditions
  • Requirements for consortium composition and stakeholder involvement
  • Specific clinical trial design and endpoint criteria

Money

Total budget around €22 million for 2026 with expected grants of €7-8 million each for up to 3 projects.

  • Total budget for 2026 — 22186000EUR
    Approximate total budget for this call in 2026
  • Minimum grant per project — 7000000EUR
    Minimum funding per successful proposal
  • Maximum grant per project — 8000000EUR
    Maximum funding per successful proposal

Application notes

  • Single-stage submission model.
  • Proposal page limits and layout as per Horizon Europe General Annexes and Application Form instructions.
  • Eligible countries as per Horizon Europe Annex B.
  • Financial and operational capacity requirements as per Horizon Europe Annex C.
  • Evaluation criteria thresholds: Excellence, Impact, Implementation each minimum 4, cumulative 12.
  • Eligible costs funded as lump sums according to Horizon Europe lump sum decision.
  • Prepare proposal following the specific application form for this call.
  • Include detailed clinical study information in the dedicated annex using provided template.
  • Justify cost items in lump sum budget if exceeding thresholds as per latest updates.
  • Submit proposal before the deadline 15 September 2026.
  • Call opening was delayed due to technical issues; confirm current submission status.
  • Applicants must include budget for networking and joint activities within the EU Cancer Mission cluster.
  • Proposals must align with EU Cancer Mission objectives and join relevant project clusters.

Derived from official EU Funding portal source · updated 2 Jul 2026, 10:58 UTC. Use this as a shortlisting aid; the official call text remains authoritative.

Related calls

These funding calls are closely related and may be worth considering as part of the same funding landscape.

Official source text

Fine print from the EU source record. Expand when you need the original wording.

Topic description

Expected Outcome: Proposals under this topic should aim to deliver results that are directed and tailored towards and contribute to all of the following expected outcomes: Patients with refractory cancers and their caregivers/families will have access to optimised, tailored and affordable immunotherapeutic interventions that increase their quality of life, across European regions, EU Member States and Associated Countries; Healthcare professionals and academia will have access to clinical evidence, on effectiveness of immunotherapeutic interventions, to deploy evidence-based treatment interventions with improved patient selection that improve outcomes in real life, i.e. in routine healthcare, for patients with refractory cancers who often present with co-morbidities; National healthcare providers, policymakers and authorities in European regions, EU Member States and Associated Countries will have the evidence to implement and reimburse optimised and affordable immunotherapeutic interventions in their healthcare systems, including in everyday medical practice. Scope: While cancer research and innovation have generated novel treatment options, patients with refractory cancers across Europe need access to more effective, affordable and tailored cancer immunotherapeutic interventions which keep up with increasing demands in a complex and fragmented oncology healthcare landscape with spiralling healthcare costs. Pragmatic clinical trials focus on choosing between care options. Pragmatic trials evaluate effectiveness of interventions in settings that more closely resemble routine, real-world settings, aiming to produce evidence directly applicable to clinical practice [1] . Proposals should address all the following: Conduct randomised or cluster-randomised academic investigator-initiated [2] pragmatic clinical trials that benefit patients with refractory cancers - at any stage of the disease, for any cancer subtype, in any age group or part of society - to deliver effective, affordable and tailored immunotherapeutic interventions for implementation by healthcare systems at the level of local communities, European regions, EU Member States and Associated Countries. All data should be disaggregated by sex, gender, age and other relevant variables, such as by measures of socio-economic status or ethnicity. Translational research is limited to supporting biomarker-informed patient stratification and the conduct and analyses of the proposed clinical trial(s). The primary and secondary endpoints of the pragmatic clinical trials should target overall survival, patient-reported outcomes and quality of life issues considered important by and for cancer patients and their caregivers/families. Such endpoints should be defined together with patients and their caregivers/families through research that stimulates social innovation and supports end-user engagement using participative research models. The chosen treatment intervention(s) should be adapted to the particular needs of the target population and to the specificities of the provision of care at local, regional, or national level, duly reflecting the diversity across EU Member States and Associated Countries. Furthermore, affordability and accessibility should be taken into account. Applicants should include an appropriate mix of stakeholders from various disciplines, sectors [3] and regional as well as national health authorities, and provide details of the clinical study(ies) in the dedicated annex using the template provided in the submission system. The successful proposals are expected to build on resources made available by the Knowledge Centre on Cancer (KCC) [4] to foster EU alignment and coordination. Successful proposals will be asked to join the 'Diagnosis and Treatment' cluster for the EU Cancer Mission [5] and should include a budget for networking, attendance at meetings, and joint activities [6] . The Commission will facilitate coordination of these activities. [1] Some examples: treatment versus active surveillance in patient management, combination of treatment interventions, determination of optimal dose and dose schedule, de-escalation of treatment intervention, comparative effectiveness of different treatment interventions. [2] Clinical trials in which a health technology (e.g. a medicinal product, a medical device, an in-vitro diagnostic medical device, a surgical or other medical intervention) is tested in humans, independently from commercial interest and for public health benefits. [3] such as physicians, academia, patients and their caregivers, patient representatives, engineers, behavioural scientists, SMEs, business networks, insurance companies, charities and foundations, research organisations, civil society. [4] Hosted by the European Commission's Joint Research Centre (JRC). Especially through the ’European Guidelines and Quality Assurance Schemes for Breast, Colorectal and Cervical Cancer Screening and Diagnosis‘, and the ’European Cancer Information System (ECIS)’ and the ’European Cancer Inequalities Registry (ECIR), see https://knowledge4policy.ec.europa.eu/cancer_en [5] To address the objectives of the EU Cancer Mission, participants will collaborate in project clusters to leverage EU-funding, increase networking across sectors and disciplines, and establish a portfolio of EU Cancer Mission R&I and policy actions. [6] Examples of those activities are research or research capacity, organising joint workshops, establishing best practices, joint communication or citizen engagement activities with projects funded under other clusters and pillars of Horizon Europe, or other EU programmes, as appropriate. Proposals are not required to include details of these activities, as they will be defined during the grant agreement preparation and during the life of the project.

Conditions and documents

General conditions

1. Admissibility Conditions: Proposal page limit and layout

described in Annex A and Annex E of the Horizon Europe Work Programme General Annexes.

Proposal page limits and layout: described in Part B of the Application Form available in the Submission System.

2. Eligible Countries

described in Annex B of the Work Programme General Annexes.

A number of non-EU/non-Associated Countries that are not automatically eligible for funding have made specific provisions for making funding available for their participants in Horizon Europe projects. See the information in the Horizon Europe Programme Guide.

3. Other Eligible Conditions

described in Annex B of the Work Programme General Annexes.

4. Financial and operational capacity and exclusion

described in Annex C of the Work Programme General Annexes.

5a. Evaluation and award: Award criteria, scoring and thresholds

are described in Annex D of the Work Programme General Annexes.

5b. Evaluation and award: Submission and evaluation processes

The thresholds for each criterion will be 4 (Excellence), 4 (Impact) and 4 (Implementation). The cumulative threshold is 12.

are described in Annex F of the Work Programme General Annexes and the Online Manual.

5c. Evaluation and award: Indicative timeline for evaluation and grant agreement

described in Annex F of the Work Programme General Annexes.

6. Legal and financial set-up of the grants

Eligible costs will take the form of a lump sum as defined in the Decision of 7 July 2021 authorising the use of lump sum contributions under the Horizon Europe Programme – the Framework Programme for Research and Innovation (2021-2027) – and in actions under the Research and Training Programme of the European Atomic Energy Community (2021-2025) [[This decision is available on the Funding and Tenders Portal, in the reference documents section for Horizon Europe, under ‘Simplified costs decisions’ or through this link: https://ec.europa.eu/info/funding-tenders/opportunities/docs/2021-2027/horizon/guidance/ls-decision_he_en.pdf]].

The granting authority may, up to 4 years after the end of the action, object to a transfer of ownership or to the exclusive licensing of results, as set out in the specific provision of Annex 5.

described in Annex G of the Work Programme General Annexes.

Specific conditions

described in the [specific topic of the Work Programme]

Support information

Online Manual is your guide on the procedures from proposal submission to managing your grant. Horizon Europe Programme Guide contains the detailed guidance to the structure, budget and political priorities of Horizon Europe. Funding & Tenders Portal FAQ – find the answers to most frequently asked questions on submission of proposals, evaluation and grant management. Research Enquiry Service – ask questions about any aspect of European research in general and the EU Research Framework Programmes in particular. National Contact Points (NCPs) – get guidance, practical information and assistance on participation in Horizon Europe. There are also NCPs in many non-EU and non-associated countries (‘third-countries’). Enterprise Europe Network – contact your EEN national contact for advice to businesses with special focus on SMEs. The support includes guidance on the EU research funding. IT Helpdesk – contact the Funding & Tenders Portal IT helpdesk for questions such as forgotten passwords, access rights and roles, technical aspects of submission of proposals, etc. European IPR Helpdesk assists you on intellectual property issues. CEN-CENELEC Research Helpdesk and ETSI Research Helpdesk – the European Standards Organisations advise you how to tackle standardisation in your project proposal. The European Charter for Researchers and the Code of Conduct for their recruitment – consult the general principles and requirements specifying the roles, responsibilities and entitlements of researchers, employers and funders of researchers. Partner Search help you find a partner organisation for your proposal.

Raw budget overview
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