Biotechnology for Healthy Ageing
Funding for biotech and pharmaceutical interventions targeting age-related diseases to promote healthy ageing and longevity.
This call supports projects developing biotech or pharmaceutical solutions to prevent or delay age-related diseases. It also funds biomarker tools and new approach methodologies for ageing research. The goal is to translate ageing research into clinical interventions and improve regulatory and societal acceptance.
Likely relevant for
- Biotechnology researchers
- Pharmaceutical developers
- Ageing and longevity researchers
- Biomedical engineers
- Regulatory affairs specialists
- Healthcare innovation projects
Project signals
What it funds
- Development of biotechnology or pharmaceutical interventions targeting fundamental ageing processes
- Proof-of-concept studies in vertebrate animal models of ageing
- Biomarker-based tools for diagnostics, prediction, or prognosis related to ageing
- New Approach Methodologies (NAMs) as alternatives to animal testing
- Regulatory pathway recommendations and societal acceptance strategies
- Consideration of biological sex and gender-specific health determinants
Expected outcomes
- Validated interventions that prevent, delay, or revert age-related diseases
- Biomarker tools linking clinical features to ageing mechanisms
- NAMs benchmarked against animal models and tested in use cases
- Recommendations for regulatory pathways for ageing interventions
- Improved citizen literacy on longevity and healthy ageing
Who can apply / participate
- Single legal entities
- Consortia of independent legal entities
- Consortia must have at least three independent legal entities from different countries
- At least one entity must be established in a Member State
- Consortia of two entities must be from two different Member States or Associated Countries
- Applicants must be established in EU Member States or Associated Countries
- Mid-caps and larger companies not permitted for single beneficiary projects
- Applicants must meet general and specific eligibility conditions in EIC Work Programme 2026
- Specific eligibility criteria for third country applicants must be checked
- Details on allowed types of entities (e.g. SMEs, research organizations) should be verified
Must check before shortlisting
- Eligibility of applicant types and consortium composition
- Compliance with page limits and submission guidelines
- Access to suitable longevity cohorts for biomarker studies
- Feasibility of clinical or preclinical validation plans
Money
Total budget around €96 million for 2026 with grants ranging from €0.5 million to €4 million each. Expected to fund about 8 projects under this call.
- Total budget for 2026 — 96000000EURShared across related Pathfinder Challenges calls
- Minimum grant per project — 500000EURMinimum funding per selected project
- Maximum grant per project — 4000000EURMaximum funding per selected project
Application notes
- Single-stage submission model.
- Proposal must meet general and specific eligibility requirements as per EIC Work Programme 2026.
- Proposal page limit: max 30 A4 pages for sections 1 to 3 of Part B.
- Consortia must comply with minimum number and country diversity requirements.
- Standard admissibility and eligibility conditions apply as per EIC Work Programme 2026.
- Prepare proposal addressing one of the three focus areas: intervention, biomarker tool, or NAM.
- Ensure access to suitable vertebrate models or longevity cohorts as applicable.
- Include plans for exploitation covering ethical, societal, economic, and regulatory aspects.
- Submit proposal via the Funding & Tenders Portal by the deadline.
- Precision nutrition, ageing clocks development, and wellness apps are out of scope.
- Sex and gender-specific health determinants must be considered.
- Small-scale clinical studies encouraged but not mandatory; clinical feasibility must be addressed.
- Applicants must verify eligibility of their entity type and consortium composition.
Derived from official EU Funding portal source · updated 2 Jul 2026, 10:27 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 Impact: This Challenge looks to accelerate the development and uptake of clinically validated interventions that target the root cause of multiple age-related morbidities. It will: Deliver biotechnology-based interventions for healthy ageing Accelerate the implementation of personalised care in ageing based on molecular phenotyping Provide recommendations for regulatory pathways addressing ageing as a target to inform developers, regulators, and other decision makers, and Improve citizen literacy on longevity. Expected Outcome: Ambitious proposals put forward under this call will deliver: Proof-of-concepts (TRL3 completed) of biotechnology-based or pharmaceutical interventions that prevents or delays the onset of, or reverts, an age-related disease in a vertebrate model system, based on the hallmarks of ageing, taking into consideration practical challenges of implementing such an intervention Tools to facilitate development or adoption of the interventions above, such as proof-of-concept validation of biomarker signatures or suitable pre-clinical models, and Approaches to address the shared regulatory hurdles and societal challenges linked to ageing-related interventions, thereby facilitating their adoption. Portfolio approach The portfolio of projects selected under this Challenge will ensure a coverage of projects developing interventions, biomarkers and NAMs, considering the following guidelines for portfolio composition: Interventions: no more than 5 projects. The portfolio of selected projects should collectively address a variety molecular and cellular processes related to ageing, and a variety of different age-related diseases. Biomarkers: no more than 3 projects. Projects will be selected to capture different application areas (diagnostic, predictive, prognostic biomarker), with preference to the inclusion of at least one diagnostic biomarker). NAMs: No more than 2 projects. Projects will be selected to capture a diversity of approaches to assess aged status in NAMs, different tissues or cell types and different use cases. The selected consortia will benefit from mutual learning, and the exchange of expertise. Consortia will be encouraged to collaborate to address the following shared challenges faced by all ageing interventions: Scientific: preclinical models; Biomarkers of healthy/unhealthy ageing Path to Market: Defining suitable regulatory pathways, and Societal: Acceptance and role of preventative / therapeutic interventions, Need for improved longevity literacy. Objective: Applicants to this Challenge will be expected to develop a proof of concept in one of the following three areas: An innovative preventative or therapeutic biotechnology-based or pharmaceutical intervention that prevents, delays or reverts the onset of a specific age-related disease. Such projects must address all of the following objectives: develop an intervention that targets a fundamental molecular or cellular process of ageing, such as the hallmarks of ageing assess the generalisability of the intervention (showing that it is applicable more broadly to ageing-related traits beyond the primary indication targeted) by assessing the impact of the intervention on another distinct trait related to ageing demonstrate proof of concept by carrying out an interventional study in a vertebrate animal model of ageing that is physiologically aged. Projects are also encouraged to include small-scale interventional clinical studies but must at a minimum anticipate how the intervention could be feasibly tested in a clinical setting, and develop a plan for exploitation, which considers ethical and societal perception, economic viability and regulatory approval. At least two of these areas, considered most relevant for the intended application, must be assessed in greater depth, suitably informing the project’s technology development and contributing to the portfolio activities. A biomarker [1] based tool to enable the responsible deployment of ageing-related interventions, taking into consideration the following: The tool should be based on previously identified potential biomarker candidates or ageing clocks. All types of biomarkers are welcome, for example digital, molecular or physiological biomarkers (such as frailty measurements), combinations of biomarkers and multimodal biomarkers); as well as biomarkers for different applications (e.g. predictive, diagnostics). Biomarker discovery is explicitly excluded The tool should integrate different measurements of multiple molecular, anatomic, physiologic, biomechanical or biochemical traits, as appropriate, to comprehensively capture the ageing process (i.e. it should not exclusively measure a single parameter/hallmark of ageing) The above selected biomarker signature should enable a clear linkage between clinical features and the mechanisms of ageing to be shown The signature should be robust to inter-individual and intra-individual variability in ageing to provide actionable, personalised insights The tool should be assessed in an initial retrospective study to establish proof-of-concept. Applicants must therefore convincingly demonstrate that they have access to suitable longevity cohorts, and The selection of the biomarkers and the development of the tool should prioritise deployment feasibility and actively incorporate feedback from potential users. A New Approach Methodology (NAM) [2] that goes beyond the current state-of-the art to enable the future development of interventions for healthy ageing. The NAM should: robustly capture the aged status of the system and the systemic/integrative nature of ageing (i.e. it should capture more than 1 molecular or cellular aspect of ageing, and more than 1 tissue type) be benchmarked against a relevant animal model of ageing, and be tested in the setting of a clearly specified use case (e.g. development of an intervention; as pre-clinical model in a regulatory setting). Precision nutrition, the development of novel ageing clocks and wellness applications fall outside the scope of this Challenge. All proposals should consider biological sex and gender-specific health determinants [3] in their development, with reproductive ageing also in scope. Scope: Ageing, the gradual decline of organismal homeostasis and of physiologic functions throughout the body and mind, is a critical shared risk factor for many ageing-related chronic diseases. The EU also has an ageing society - by 2050, the share of 85+ year-olds in the EU is expected to more than double, but extended life expectancy is not matched with years spent in good health, which currently stands at 70.5 years. This will present significant social, economic and healthcare challenges and thus calls for interventions that will promote healthy longevity, as well as tools that will enable the adoption of these interventions. Over the past decades basic research has identified hallmarks and cellular mechanisms of ageing, creating the basis for biotechnology-based or pharmaceutical therapeutic interventions, such as targeting cellular maintenance pathways, stem cell exhaustion, cellular senescence or metabolic fitness. Nonetheless, translating these insights into clinical interventions has had a low success rate, partially due to the difficulty of: Translating approaches from model systems Identifying when to intervene Rigorous validation, and End-to-end considerations of implementation (i.e. the delivery of an intervention). This Challenge therefore looks to translate decades of ageing research into tangible biopharmaceutical solutions for healthy ageing [1] Biomarkers are biological characteristics, which can be molecular, anatomic, physiologic, or biochemical. These characteristics can be measured and evaluated objectively. They act as indicators of a normal or a pathogenic biological process. They allow the assessment of the pharmacological response to a therapeutic intervention. A biomarker shows a specific physical trait or a measurable biologically produced change in the body that is linked to a disease or a particular health condition. A biomarker may be used to assess or detect a specific disease as early as possible (diagnostic biomarker), the risk of developing a disease (susceptibility/risk biomarker), the evolution of a disease (prognostic biomarker) – but it can also predict response to a given treatment including potential toxicity (predictive biomarker) [2] New approach methodologies (NAMs) represent potential alternatives to animal testing in the non-clinical development phase of new medicines. They may include human organoids or microphysiological systems (e.g. organ-on-chip, disease-on-chip), in chemico methods, digital twins, virtual patient simulations, AI-enhanced predictive models, mechanistic or integrated in silico platforms, 3D- advanced human tissue model [3] Sex: Refers to biological characteristics (including genetic, hormonal, physiological, anatomical) that distinguish between male, female, and intersex (in humans) or hermaphrodite (in non-human animals). Gender: Refers to socio-cultural norms, identities and relations that, together, shape and sanction what are considered “feminine” and “masculine” behaviours, and structure societies and organisations. From Gender In EU Research and Innovation (https://rea.ec.europa.eu/gender-eu-research-and-innovation_en)
Conditions and documents
General conditions
1. Admissibility conditions: Proposal page limit and layout
In order to apply, your proposal must meet the general eligibility requirements (see Annex 2 of EIC Work Programme 2026) as well as specific eligibility requirements for the Challenge (please see the Topic description above).
Please check for particular elements (e.g., specific application focus or technology) in the respective Challenge chapter.
The EIC Pathfinder Challenges support collaborative or individual research and innovation from consortia or from single legal entities established in a Member State or an Associated Country (unless stated otherwise in the specific Challenge chapter). In case of a consortium your proposal must be submitted by the coordinator on behalf of the consortium. Consortia of two entities must be comprised of independent legal entities from two different Member States or Associated Countries. Consortia of three or more entities must include as beneficiaries at least three legal entities, independent from each other and each established in a different country as follows:
- at least one legal entity established in a Member State; and
- at least two other independent legal entities, each established in different Member States or Associated Countries.
The legal entities may for example be universities, research organisations, SMEs, start-ups, natural persons. In the case of single beneficiary projects, mid-caps and larger companies will not be permitted.
Applications with elements that concern the evolution of European communication networks (5G, post-5G and other technologies linked to the evolution of European communication networks) will be subject to restriction for the protection of European communication networks (see Annex II – Section B1).
The standard admissibility and eligibility conditions and the eligibility of applicants from third countries are detailed in Annex 2.
Proposal page limit and layout:
Described in Part B of the Application Form available in the Submission System.
Sections 1 to 3 of the part B of your proposal, corresponding respectively to the evaluation criteria Excellence, Impact, and Quality and Efficiency of the Implementation, must consist of a maximum of 30 format A4 pages. Excess pages will be automatically made invisible, and will not be taken into consideration by the evaluators. Please also consult Annex 2 of the EIC Work Programme 2026.
2. Eligible countries
Described in Annex 2 of the EIC Work Programme 2026.
3. Other Eligibility Conditions
Described in Annex 2 of the EIC Work Programme 2026.
4. Financial and operational capacity and exclusion
Described in Annex 2 of the EIC Work Programme 2026.
5a. Evaluation and award: Award criteria, scoring and thresholds
Described in Section II of the EIC Work Programme 2026.
5b. Evaluation and award: Submission and evaluation processes
Described in Section II of the EIC Work Programme 2026 and the Online Manual.
5c. Evaluation and award: Indicative timeline for evaluation and grant agreement
Described in Section II of the EIC Work Programme 2026.
6. Legal and financial set-up of the grants
Please refer to the Lump Sum Model Grant Agreement (Lump Sum MGA) used for Lump Sum EIC actions under Horizon Europe.
Specific conditions
Described in the EIC Work Programme 2026.
Call Documents:
Frequently Asked Questions (FAQs)
Standard application form (HE EIC Pathfinder Challenges)
Standard evaluation form (HE EIC Pathfinder Challenges)
Challenge Guide: Biotechnology for Healthy Ageing
Model grant agreement (MGA):
Call-specific instructions
Additional documents:
HE Framework Programme 2021/695
HE Specific Programme Decision 2021/764
EU Financial Regulation 2018/1046
Rules for Legal Entity Validation, LEAR Appointment and Financial Capacity Assessment
EU Grants AGA — Annotated Model Grant Agreement
Funding & Tenders Portal Online Manual
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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