Subvenciones y ayudas para entidades sociales

13926
convocatorias abiertas
9
países
12
fuentes oficiales

Reunimos en un solo lugar las convocatorias públicas de subvenciones de España, la Unión Europea y otros países. Cada ficha indica el importe, el plazo real y quién puede solicitarla, para que sepas de un vistazo si tu entidad encaja.

Subvenciones por tipo de entidad

Convocatorias abiertas

13.926 convocatorias · ordenadas por Cierran antes

🇺🇸Estados UnidosABIERTA
97 días

National Science Foundation Translation to Practice

Estados Unidos · US

Quién puede pedirla Others (see text field entitled "Additional Information on Eligibility" for clarification)

The U.S. NSF Directorate for Technology, Innovation and Partnerships (NSF TIP) partners across sectors to advance three primary focus areas – accelerating technology translation and development, fostering regional innovation and economic growth, and preparing the American workforce for future high-wage jobs in STEM fields. The translation of research to practice ensures that the insights and innovations developed through scientific study and experimentation have tangible, positive impacts for the Nation. These impacts include improving the quality of life, promoting economic and job growth, ensuring national security, and maintaining global competitiveness. Indeed, scientific and engineering breakthroughs have the potential to address critical societal challenges in industries such as aerospace, agriculture, communications, education, energy, healthcare, national security, and transportation – but the translation of discoveries and innovations from the laboratory to society often takes many forms including non-linear pathways. The NSF TTP program was developed with several goals in mind: To identify and support use-inspired research and translational activities enabling a continuum from foundational research to practice; To develop partnerships and collaborations between institutions of higher education and other entities (e.g., industry, state/local/national government agencies, philanthropies, open-source ecosystems, for-benefit, for-profit and non-profit organizations, international organizations, etc.); To promote and advance the education and training of students and postdoctoral researchers, encouraging the participation of all Americans in STEM including innovation and entrepreneurship; and To identify future customer needs and opportunities and bring these to the forefront in the conduct of use-inspired research and translational activities. The NSF TTP program offers three tracks that represent different starting points or stages in moving discoveries and innovations from the laboratory to practice: NSF TTP-Explore (NSF TTP-E) is a pilot track that is likely to be the first step for researchers seeking to translate their basic research to practice. To be eligible for the NSF TTP-E track, proposers must have an active, eligible, NSF research award (see Eligibility Information for further details). TTP-E is designed to encourage current, eligible NSF awardees to intentionally pursue applications of their research with the potential for societal impact. The NSF TTP-E track provides the opportunity to obtain an extension of the initial award period of a current NSF award for up to two years in order to offer investigators an opportunity to explore adventurous, high-risk, use-inspired research and initial translational activities as the starting point for translation that was not covered by the original research award. NSF TTP-Translate (NSF TTP-T) starts with use-inspired research and initial translational activities and further matures the idea(s), iterates and improves the solution(s), and lowers the barrier(s) to effective translation of research from lab to practice. NSF TTP-Partner (NSF TTP-P) supports translational efforts that demand one or more partnerships for technology development and deployment. Here, strategic partnerships with stakeholders beyond U.S. institutions of higher education are essential ingredients for success and may include industry partners, government entities at all levels, philanthropies, international organizations, or other groups associated with large scale productization and distribution. The NSF TTP-P track requires an NSF-Catalyzed Partnership with an organization that will assist in the translation to practice. In addition to the Principal Investigator (PI), NSF TTP-P proposals must include a co-PI or Senior/Key Personnel who is a member or employee of the NSF-Catalyzed Partner. Partnerships with U.S. institutions of higher education are valued, but NSF TTP strongly prioritizes NSF-Catalyzed Partnerships that are able to help bring the product, process, or service to the market, potentially through licensing agreements, startup or small business formation, incorporation into an existing open-source ecosystem, development into standards setting arrangements, etc.

2.000.000 US$17/11/2026
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🇺🇸Estados UnidosABIERTA
97 días

Prevention and Intervention Approaches for Fetal Alcohol Spectrum Disorders (R61/R33 Clinical Trial Optional)

Estados Unidos · US

Quién puede pedirla Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education · Special district governments · Public housing authorities/Indian housing authorities · County governments · Independent school districts · Public and State controlled institutions of higher education · Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education · Private institutions of higher education · Others (see text field entitled "Additional Information on Eligibility" for clarification) · City or township governments · For profit organizations other than small businesses · Native American tribal organizations (other than Federally recognized tribal governments) · Native American tribal governments (Federally recognized) · State governments · Small businesses

This Notice of Funding Opportunity (NOFO) focuses on prevention and intervention strategies for fetal alcohol spectrum disorders (FASD) throughout the lifespan. The intent of this NOFO is to support research that advances (1) prevention approaches to reduce prenatal alcohol exposure and the incidence of FASD and that (2) interventions for FASD. These objectives will be accomplished with the Exploratory/Developmental Phased Award (R61/R33) mechanism, clinical trial optional. The R61 phase will support pilot studies or secondary data analysis for hypothesis development and feasibility, and research testing the hypotheses can be expanded in the R33 phase. The transition to the R33 phase will be determined by NIAAA program staff after evaluation of the achievement of specific milestones set for the R61 phase. Highest priority will be given to applications with clinical trials. Applicants interested in planning clinical trials or adding to current projects may also consider NOFO (TEMP-23832, the R34 option).

Según convocatoria17/11/2026
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🇺🇸Estados UnidosABIERTA
97 días

Feasibility Clinical Trials of Mind and Body Interventions for NCCIH High Priority Research Topics (R34 Clinical Trial Required)

Estados Unidos · US

Quién puede pedirla Public and State controlled institutions of higher education · Private institutions of higher education · Others (see text field entitled "Additional Information on Eligibility" for clarification) · County governments · Native American tribal governments (Federally recognized) · Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education · Special district governments · State governments · Small businesses · Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education · Independent school districts · City or township governments · Native American tribal organizations (other than Federally recognized tribal governments) · Public housing authorities/Indian housing authorities · For profit organizations other than small businesses

The goal of this notice of funding opportunity (NOFO) is to support feasibility trials of complementary and integrative health approaches with physical and/or psychological therapeutic inputs (often called mind and body interventions) for conditions that have been identified by NCCIH as high-priority research topics. This funding opportunity is intended to support feasibility clinical trials that provide new information that are scientifically necessary for the planning and conduct of a subsequent clinical efficacy or effectiveness study, pragmatic trial, or dissemination and implementation trial within NCCIHs mission. NCCIH expects that applications to this NOFO will describe the planned future clinical trial and in so doing demonstrate that the proposed (R34) research is scientifically necessary to design or plan the subsequent competitive full-scale clinical trial. Under this R34, the data collected should be used to fill gaps in scientific knowledge necessary to develop a competitive full-scale clinical trial, including, but not limited to the following: examining feasibility and acceptability of interventions lacking published data; tailoring or adapting the content or structure of an intervention to a specific population, modality, or setting; refining the intervention to determine the most appropriate frequency or duration; determining feasibility of recruitment, retention, and data collection procedures; refining and assessing the feasibility of protocolized multi-component interventions; or examining acceptability and adherence of control conditions. The subsequent full-scale clinical trial should have the potential to make a significant impact on public health. Prior to submitting to this NOFO, applicants are encouraged to contact the appropriate NCCIH Scientific/Research contact person for the science area of the planned application.

Según convocatoria17/11/2026
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🇺🇸Estados UnidosABIERTA
97 días

Investigator Initiated Clinical Trials of Complementary and Integrative Interventions Delivered Remotely or via mHealth (R01 Clinical Trial Required)

Estados Unidos · US

Quién puede pedirla Native American tribal organizations (other than Federally recognized tribal governments) · For profit organizations other than small businesses · County governments · Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education · Small businesses · Others (see text field entitled "Additional Information on Eligibility" for clarification) · Native American tribal governments (Federally recognized) · Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education · Private institutions of higher education · Special district governments · Independent school districts · Public and State controlled institutions of higher education · State governments · City or township governments · Public housing authorities/Indian housing authorities

This Notice of Funding Opportunity (NOFO) encourages applications for investigator-initiated fully remotely delivered and conducted clinical trials to assess the efficacy or effectiveness of complementary and integrative health interventions in NCCIH- designated areas of high research priority. Applications submitted under this NOFO are expected to propose a remotely delivered and conducted fully powered clinical trial with no in-person contact between research staff and study participants and may utilize mHealth tools or technologies. Applicants must provide justification for the remotely delivered approach and provide preliminary data on the feasibility and safety of the approach, along with evidence that the intervention has promise of clinical benefit. Applicants are encouraged to contact the appropriate NCCIH Scientific/Research contact for the area of science for which they are planning to develop an application prior to submitting to this NOFO.

Según convocatoria17/11/2026
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🇺🇸Estados UnidosABIERTA
97 días

NCCIH Multi-Site Feasibility Clinical Trials of Mind and Body Interventions (R01 Clinical Trial Required)

Estados Unidos · US

Quién puede pedirla For profit organizations other than small businesses · Independent school districts · Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education · State governments · Native American tribal organizations (other than Federally recognized tribal governments) · Special district governments · Public and State controlled institutions of higher education · Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education · Private institutions of higher education · Small businesses · County governments · City or township governments · Public housing authorities/Indian housing authorities · Native American tribal governments (Federally recognized) · Others (see text field entitled "Additional Information on Eligibility" for clarification)

This notice of funding opportunity (NOFO) invites applications for investigator-initiated clinical trials of complementary and integrative health approaches with physical and/or psychological therapeutic inputs (often called mind and body interventions) in NCCIH-designated areas of high research priority. Applications submitted under this NOFO are expected to propose a multisite feasibility clinical trial that will provide new information that is scientifically necessary for the planning and conduct of a subsequent clinical efficacy or effectiveness study, pragmatic trial, or dissemination and implementation trial within NCCIHs mission. NCCIH expects that applications to this NOFO will describe the planned future clinical trial and in so doing demonstrate that the proposed (R01) research is scientifically necessary to design or plan the subsequent fully powered, full-scale clinical trial. Under this R01, the data collected should be used to fill gaps in scientific knowledge, including, but not limited to the following: assessing whether the intervention can be delivered with fidelity across sites; demonstrating feasibility of recruitment, accrual, and randomization of participants across sites; demonstrating participant adherence to the intervention, as well as retention of participants throughout the study across sites; refining and assessing the feasibility of protocolized multimodal interventions, and/or demonstrating feasibility of data collection across sites in preparation for a future fully powered, multisite efficacy or effectiveness trial. The need for multisite feasibility trials is expected to be justified by sufficient preliminary data from previous single site feasibility or acceptability trial(s) or the published literature. The data collected should be used to fill gaps in scientific knowledge and be necessary to develop a competitive fully powered multisite clinical trial that has the potential to make a significant impact on public health.

350.000 US$17/11/2026
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🇺🇸Estados UnidosABIERTA
97 días

Secondary Analysis and Integration of Existing Data to Elucidate Cancer Risk and Related Outcomes (R21 Clinical Trials Not Allowed)

Estados Unidos · US

Quién puede pedirla Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education · Native American tribal governments (Federally recognized) · Special district governments · Private institutions of higher education · State governments · For profit organizations other than small businesses · Public and State controlled institutions of higher education · City or township governments · County governments · Independent school districts · Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education · Native American tribal organizations (other than Federally recognized tribal governments) · Small businesses · Others (see text field entitled "Additional Information on Eligibility" for clarification) · Public housing authorities/Indian housing authorities

Through this Notice of Funding Opportunity (NOFO), the National Cancer Institute (NCI) along with other participating Institutes encourages submission of applications proposing to conduct secondary data analysis and integration of existing datasets and database resources, with the ultimate aim to elucidate cancer risk and related outcomes (e.g., risk prediction or reduction, survival, or response to treatment, etc.). The goal of this initiative is to address key scientific questions relevant to cancer by supporting the analysis of existing clinical, environmental, surveillance, health services, vital statistics, behavioral, lifestyle, genomic, and molecular profiles data. Applicants are encouraged to leverage and perform innovative analyses of the existing data. Applications may include new research aims that are being addressed with existing data, new or advanced methods of analyses, or novel combinations and integration of datasets that allow the exploration of important scientific questions in cancer research.

200.000 US$17/11/2026
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🇪🇸EspañaABIERTA
97 días

PRIMERA CONVOCATORIA DEL PROGRAMA DE INCENTIVOS A PROYECTOS SINGULARES INNOVADORES DE AHORRO Y EFICIENCIA ENERGÉTICA (INNOVAE)

ESTADO - MINISTERIO PARA LA TRANSICIÓN ECOLÓGICA Y EL RETO DEMOGRÁFICO - INSTITUTO PARA LA DIVERSIFICACIÓN Y AHORRO DE LA ENERGÍA (IDAE) ·

Industria y Energía

115.000.000 €18/11/2026

Ejecución: 15/9/2026

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🇺🇸Estados UnidosABIERTA
98 días

DOW Combat Readiness – Medical Research Program Translational Research Award

Estados Unidos · US

Quién puede pedirla Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled "Additional Information on Eligibility"

Summary: The fiscal year 2026 (FY26) Combat Readiness – Medical Research Program (CRRP) Translational Research Award (TRA) supports hypothesis-driven innovative, high-impact translational research that will accelerate the movement of promising ideas and/or technologies in trauma care into solutions to maximize casualty survivability, improve patient care closer to the point of injury and/or trauma care guidelines. Preliminary data are required. Research using well-validated animal models is allowed. Distinctive Features: • **NEW for FY26** An investigator may be named as the Principal Investigator (PI) on only one FY26 CRRP TRA application. • Research supported by the FY26 CRRP TRA must represent a mature, translational research effort with a minimum biomedical technology readiness level (TRL) of 4 or knowledge readiness level (KRL) of 4.

4.370.000 US$18/11/2026
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🇺🇸Estados UnidosABIERTA
98 días

DoW Orthopaedic, Clinical Research Award

Estados Unidos · US

Quién puede pedirla Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled "Additional Information on Eligibility"

Summary: The fiscal year 2026 (FY26) Orthopaedic Research Program (ORP) Clinical Research Award (CRA) seeks clinical research that evaluates orthopaedic-specific factors and interventions. The ORP intends for research supported by this mechanism to generate clinically useful evidence with potential to optimize patient outcomes and inform clinical care or policy. Applications must address how the proposed research will impact patient care and reduce the burden of orthopaedic injury and sequela. The ORP expects that research findings benefit Service Members, their families, Veterans and the general public. To meet the intent of the award mechanism, applications must specifically address at least one of the FY26 ORP CRA Focus Areas. Distinctive Features: · The CRA offers two research levels. Research Level 1 (RL1) supports clinical research in the following FY26 ORP focus areas: · Ligamentous Trauma · Osseointegration Outcomes · Return-to-Duty Strategies · Military Women’s Health Research Level 2 (RL2) supports clinical trials in the following FY26 ORP focus areas: · Ligamentous Trauma · Limb Stabilization and Protection · Return-to-Duty Strategies

13.600.000 US$18/11/2026
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🇺🇸Estados UnidosABIERTA
98 días

DoW Orthopaedic, Applied Research Award

Estados Unidos · US

Quién puede pedirla Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled "Additional Information on Eligibility"

Summary: The Orthopaedic Research Program (ORP) Applied Research Award (ARA) seeks applied research applications focused on advancing optimal treatment and restoration of function for individuals with orthopaedic injuries sustained during combat or service-related activities. Distinctive Features: • Applied research is defined as work that refines concepts and ideas into potential solutions with a view toward evaluating technical feasibility of promising new knowledge products, pharmacologic agents, behavioral and rehabilitation interventions, diagnostic and therapeutic techniques, clinical guidance and/or emerging approaches and technologies. • Preliminary data is required. • Military relevance : the ORP expects that research findings benefit Service Members, their families, Veterans and the general public. • Clinical research is not allowed.

3.800.000 US$18/11/2026
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🇺🇸Estados UnidosABIERTA
98 días

DoW Rare Cancers Resource and Community Development Award

Estados Unidos · US

Quién puede pedirla Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled "Additional Information on Eligibility"

Summary: The fiscal year 2026 (FY26) Rare Cancers Research Program (RCRP) Resource and Community Development Award (RCDA) supports the development of research resources and clinical or preclinical datasets that will advance the field of rare cancers research and ultimately improve outcomes for individuals with rare cancers. Research supporting this funding opportunity should fill one of the following major gaps: Lack of research and clinical resources, including patient tissues, cell and tumor models. Lack of communication and dissemination strategies within scientific and patient communities for sharing rare cancers research and clinical findings. Lack of infrastructure for sharing data and other resources. Lack of therapeutics and mechanistic research to inform treatment development. Distinctive Features: Documentation of plans for engagement and partnerships with Patient Advocates throughout the life cycle of the research study from development of the research question through execution of the study. Community building and enhancement are key components. A description of the dissemination and sustainability of the platform for scientific and/or clinical and patient community is required. Preliminary data are not required but may be included to address feasibility.

5.600.000 US$18/11/2026
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🇺🇸Estados UnidosABIERTA
98 días

DoW Rare Cancers Idea Development Award

Estados Unidos · US

Quién puede pedirla Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled "Additional Information on Eligibility"

Summary: The fiscal year 2026 (FY26) Rare Cancers Research Program (RCRP) Idea Development Award (IDA) promotes ideas that are ready for further development and have the potential to yield high-impact findings and new avenues of investigation. Distinctive Features: The RCRP encourages applicants to include an exploratory aim or sub-aim to support any necessary discovery-driven research. Preliminary data with disease-specific rationale are required. However, these data do not necessarily need to originate from studies of the proposed rare cancer type(s)/subtype(s) under study. Research should have high potential impact on rare cancers and the patient community.

7.350.000 US$18/11/2026
Ver
🇺🇸Estados UnidosABIERTA
98 días

Fundación Nacional de Ciencias Fomentando Redes Interdisciplinarias para Desarrollar Soluciones Emergentes y Adaptables (FINDERS FOUNDRY)

Estados Unidos · US

Quién puede pedirla Others (see text field entitled "Additional Information on Eligibility" for clarification)

El programa NSF FINDERS FOUNDRY apoya la colaboración entre educadores de K-12, tecnólogos e investigadores para desarrollar soluciones innovadoras a desafíos persistentes en el aprendizaje y el desarrollo de la fuerza laboral. Estos desafíos son identificados por estudiantes de K-12, familias y educadores. El programa tiene como objetivo crear y escalar prácticas, herramientas y tecnologías basadas en evidencia que mejoren los resultados del aprendizaje y preparen a los estudiantes para un futuro digital impulsado por la Inteligencia Artificial (IA). Un enfoque clave es la exposición temprana a la IA para fomentar la curiosidad, la comprensión y la preparación para futuras carreras. El programa fomenta asociaciones entre sectores (escuelas, universidades, industria, gobierno y organizaciones sin fines de lucro) para codiseñar soluciones receptivas basadas en tecnología. El programa NSF FINDERS FOUNDRY incluye dos fases: Planificación y Desarrollo. Las propuestas de Planificación ayudan a los equipos a explorar una de varias áreas de enfoque. Solo los equipos a los que se les otorgan subvenciones de Planificación pueden presentar propuestas de Desarrollo, que apoyan el crecimiento y la implementación de ideas prometedoras. El programa se alinea con las prioridades nacionales, incluida la Orden Ejecutiva 14277, “Promoción de la Educación en Inteligencia Artificial para la Juventud Estadounidense ” (23 de abril de 2025), y la Ley CHIPS y Ciencia de 2022, Ley Pública 117-167 , Secciones 10381-10383 y…

8.500.000 US$18/11/2026
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🇺🇸Estados UnidosABIERTA
98 días

Ethical, Legal and Social Implications (ELSI) Research (R01 Clinical Trial Optional)

Estados Unidos · US

Quién puede pedirla County governments · Native American tribal organizations (other than Federally recognized tribal governments) · Public housing authorities/Indian housing authorities · Special district governments · For profit organizations other than small businesses · Public and State controlled institutions of higher education · Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education · State governments · Small businesses · Native American tribal governments (Federally recognized) · Private institutions of higher education · Independent school districts · Others (see text field entitled "Additional Information on Eligibility" for clarification) · City or township governments · Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education

The purpose of this NOFO is to invite Research Project (R01) applications that propose to study the ethical, legal, and social implications (ELSI) of human genetics and genomics. Applications may propose studies using either single or mixed methods. Approaches may include but are not limited to empirical qualitative and quantitative methods, as well as conceptual, legal, and normative analyses. Direct involvement of key stakeholders where appropriate is encouraged. This Notice of Funding Opportunity (NOFO) requires a Plan for Enhancing Diverse Perspectives (PEDP) as part of the application. Applications without a PEDP will not be reviewed.

Según convocatoria18/11/2026
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🇺🇸Estados UnidosABIERTA
98 días

Ethical, Legal and Social Implications (ELSI) Exploratory/Developmental Research Grant (R21 Clinical Trial Optional)

Estados Unidos · US

Quién puede pedirla State governments · Public and State controlled institutions of higher education · Private institutions of higher education · Public housing authorities/Indian housing authorities · Others (see text field entitled "Additional Information on Eligibility" for clarification) · For profit organizations other than small businesses · Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education · Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education · Native American tribal governments (Federally recognized) · Small businesses · Independent school districts · County governments · Native American tribal organizations (other than Federally recognized tribal governments) · City or township governments · Special district governments

The purpose of this NOFO is to invite Exploratory/Developmental Research Grant (R21) applications that propose to study the ethical, legal, and social implications (ELSI) of human genetics and genomics. Applications may propose studies using either single or mixed methods. Approaches may include but are not limited to empirical qualitative and quantitative methods, as well as conceptual, legal, and normative analyses. Direct involvement of key stakeholders where appropriate is encouraged. Of particular interest are studies that explore the implications of new or emerging genomic technologies or novel uses of genomic information.

Según convocatoria18/11/2026
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🇺🇸Estados UnidosABIERTA
99 días

DoW Toxic Exposures Investigator Initiated Research Award

Estados Unidos · US

Quién puede pedirla Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled "Additional Information on Eligibility"

Summary: The fiscal year 2026 Toxic Exposures Research Program (TERP) Investigator-Initiated Research Award (IIRA) is intended to support studies that will make an important contribution toward research and/or patient care for diseases or conditions associated with military-related toxic exposures. Research projects may focus on any phase of research from basic laboratory research through translational research, including preclinical studies in animal models and human subjects, as well as correlative studies associated with an existing clinical trial. New Approach Methodologies may also be used. https://cdmrp.health.mil/pubs/press/2026/terppreann

2.400.000 US$19/11/2026
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🇺🇸Estados UnidosABIERTA
99 días

DoW Toxic Exposures Translational Research Award

Estados Unidos · US

Quién puede pedirla Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled "Additional Information on Eligibility"

Summary: The intent of the fiscal year 2026 (FY26) Toxic Exposures Research Program (TERP) Translational Research Award (TRA) is to support translational research that will accelerate the movement of promising ideas in military-related toxic exposure research into clinical applications, including health care products, interventions, technologies and/or clinical practice guidelines. Translational research may be defined as an integration of basic science and clinical observations. New Approach Methodologies may also be used. Applications should provide evidence for the reciprocal transfer of information between basic and clinical science, or vice versa, in developing and implementing the research plan. Distinctive Features: To encourage applications that include meaningful and productive collaborations, the FY26 TERP TRA includes a Partnering Principal Investigator Option (PPIO). One Principal Investigator (PI) is identified as the initiating PI, and an additional PI may be identified as a Partnering PI. If recommended for funding, each PI will be named on separate awards. The intent is to support interdisciplinary partnerships, such as those between clinicians and research scientists, that will accelerate the movement of promising ideas into clinical applications. Partnering should significantly advance the research beyond what would be possible through individual efforts. https://cdmrp.health.mil/pubs/press/2026/terppreann

6.000.000 US$19/11/2026
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🇺🇸Estados UnidosABIERTA
99 días

DoW Toxic Exposures Clinical Trial Award

Estados Unidos · US

Quién puede pedirla Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled "Additional Information on Eligibility"

Summary: The fiscal year 2026 (FY26) Toxic Exposures Research Program (TERP) Clinical Trial Award (CTA) mechanism supports the advancement, execution, and analysis of clinical trials with the potential to have a significant impact on the prevention, treatment, or management of symptoms, diseases or conditions associated with or resulting from military-related toxic exposures. Proposed projects may range from small proof-of-concept clinical trials (e.g., pilot, first-in-human, phase 0) designed to demonstrate the feasibility or inform the design of more advanced trials, through large-scale trials (including pragmatic clinical trials) to determine efficacy in relevant patient populations. Distinctive Features: To encourage applications that include meaningful and productive collaborations, the FY26 TERP CTA includes a Partnering Principal Investigator Option (PPIO) . One Principal Investigator (PI) is identified as the initiating PI, and an additional PI may be identified as a Partnering PI. If recommended for funding, each PI will be named on separate awards. The intent is to support interdisciplinary partnerships, such as those between clinicians and research scientists, that will accelerate the movement of promising interventions/​knowledge products into clinical applications. Partnering should significantly advance the research beyond what would be possible through independent efforts. https://cdmrp.health.mil/pubs/press/2026/terppreann

4.500.000 US$19/11/2026
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🇺🇸Estados UnidosABIERTA
99 días

Seamless Early-Stage Clinical Drug Development (Phase 1 to 2a) for Novel therapeutic Agents for the Spectrum of Alzheimer's Disease (AD) and AD-related Dementias (ADRD) (UG3/UH3 Clinical Trial Required)

Estados Unidos · US

Quién puede pedirla City or township governments · Native American tribal organizations (other than Federally recognized tribal governments) · Private institutions of higher education · For profit organizations other than small businesses · Native American tribal governments (Federally recognized) · Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education · Public and State controlled institutions of higher education · Independent school districts · Public housing authorities/Indian housing authorities · Special district governments · Small businesses · County governments · State governments · Others (see text field entitled "Additional Information on Eligibility" for clarification) · Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education

The purpose of this Notice of Funding Opportunity (NOFO) is to invite applications that bundle independent protocols for phase 1 clinical trials with phase 1b/phase 2a clinical trials to streamline the early-stage evaluation of promising pharmacological interventions for Alzheimer's disease (AD) and Alzheimer's disease-related Dementias (ADRD). Candidate interventions evaluated through this program, which can include small molecules or biologics for example, must engage non-amyloid/non-tau mechanisms and aim to address cognitive and/or neuropsychiatric symptoms in individuals across the spectrum from pre-symptomatic to more severe stages of disease. This NOFO uses the UG3/UH3 phased award mechanism and proposals must include prespecified, go/no-go safety and tolerability milestones that gate the advance from phase 1 to latter stages of clinical development.

Según convocatoria19/11/2026
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🇺🇸Estados UnidosABIERTA
99 días

Ensayos Clínicos y Estudios de Biomarcadores de NIH StrokeNet para el Tratamiento, Recuperación y Prevención del Accidente Cerebrovascular (UG3/UH3 Ensayo Clínico Opcional)

Estados Unidos · US

Quién puede pedirla City or township governments · Special district governments · Public housing authorities/Indian housing authorities · Native American tribal governments (Federally recognized) · Independent school districts · Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education · Public and State controlled institutions of higher education · County governments · Native American tribal organizations (other than Federally recognized tribal governments) · Private institutions of higher education · State governments · Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education · Others (see text field entitled "Additional Information on Eligibility" for clarification) · Small businesses · For profit organizations other than small businesses

Esta NOFO fomenta las solicitudes para ensayos clínicos exploratorios y confirmatorios multicéntricos centrados en intervenciones prometedoras; estudios de validación de biomarcadores o medidas de resultado que son inmediatamente preparatorios para ensayos en la prevención, tratamiento y recuperación del accidente cerebrovascular; y estudios auxiliares diseñados para agregar objetivos científicos a estudios activos que se realizan dentro de StrokeNet. Los solicitantes seleccionados colaborarán y realizarán el estudio dentro de NIH StrokeNet. Después de la revisión por pares, NINDS priorizará los estudios con la puntuación más alta para ser realizados en la infraestructura de NIH StrokeNet. El Centro Coordinador Nacional (NCC) de NIH StrokeNet trabajará con el solicitante seleccionado para implementar el estudio propuesto de manera eficiente y el Centro Nacional de Gestión de Datos (NDMC) proporcionará apoyo estadístico y de gestión de datos. Los Centros Coordinadores Regionales (RCC) de NIH StrokeNet y sus sitios clínicos afiliados proporcionarán apoyo de reclutamiento/retención, así como la implementación in situ del protocolo clínico.

Según convocatoria19/11/2026
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99 días

Decreto Foral 73/2026, de 23 de julio, de la Diputación Foral de Bizkaia, por el que se aprueban las bases reguladoras y la convocatoria de los Premios al Reto de Periodismo de Datos 2026.

LOCAL - DIPUTACIÓN FORAL DE BIZKAIA - DIPUTACIÓN FORAL DE BIZKAIA ·

Educación

6750 €20/11/2026

Ejecución: 28/7/2026

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99 días

Convocatoria de ayudas para la elaboración de Trabajos Fin de Grado y Trabajos de Fin de Máster del Instituto de Investigación en Energías Renovables de la Universidad de Castilla-La Mancha del curso académico 2026/2027

OTROS - UNIVERSIDAD DE CASTILLA-LA MANCHA ·

Educación

1800 €20/11/2026

Ejecución: 15/9/2026

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99 días

III CONCURSO PROVINCIAL DE BELENES DE LA DIPUTACIÓN PROVINCIAL DE GRANADA. Navidad 2026 – 2027

LOCAL - DIPUTACIÓN PROV. DE GRANADA - DIPUTACIÓN PROVINCIAL DE GRANADA ·

Cultura

3000 €20/11/2026
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99 días

CONVOCATORIA SUBVENCIONES CONCURRENCIA COMPETITIVA PARA GASTOS VIVIENDA DE PERSONAS PROPIETARIAS, AÑO 2026

LOCAL - GARRIGA, LA - AYUNTAMIENTO DE GARRIGA, LA ·

Otras Prestaciones económicas

10.000 €20/11/2026

Ejecución: 10/6/2026

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