Funding Opportunity

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Through this NOFO, the NCI encourages the submission of exploratory/ developmental research grant (R21) applications that focus on different aspects of cancer control by modifying behavior, screening, and understanding etiologic factors contributing to the development of cancer, and developing ways to control cancer.
The purpose of this NOFO is to support confirmatory efficacy testing of non-pharmacological preventive and therapeutic interventions, and under certain conditions, selected pharmacological interventions for mental disorders in adults and children through an experimental therapeutics approach.
The purpose of this NOFO is to encourage applications seeking to develop the next generation of brain stimulation devices for treating mental health disorders. Applications are encouraged that will either 1) develop novel brain stimulation devices or 2) significantly enhance, by means of hardware/software improvements, the effectiveness of brain stimulation devices that are U.S. Food and Drug Administration (FDA)-approved or cleared.
This NOFO invites Exploratory/ Developmental Research Grant (R21) applications that propose to study the ethical, legal and social implications (ELSI) of human genetic or genomic research. Applications may propose studies using either single or mixed methods, that break new ground, extend previous discoveries in new directions, or develop preliminary data in preparation for larger studies.
The General Research Grant is open to qualified investigators proposing projects that align with FARA Research Priorities.
The National Cancer Institute (NCI) invites applications for support of investigator-initiated clinical trials related to the programmatic interests of the NCI Division of Cancer Prevention and/or the NCI Division of Cancer Control and Population Sciences that have the potential to reduce the burden of cancer through improvements in early detection, screening, prevention and interception, healthcare delivery, quality of life, and/or survivorship related to cancer; with such attributes, the proposed studies should also have the potential to improve clinical practice and/or public health.
The proposed project must involve at least 1 clinical trial related to the scientific interests of one or more of the following research programs: Cancer Therapy Evaluation Program, Cancer Imaging Program, Cancer Diagnosis Program, Radiation Research Program, Complementary and Alternative Medicine Program and/or the HIV and AIDS Malignancies Research Programs. Applicants may propose to conduct an early phase trial by itself, or in combination with another research aim(s) as appropriate.
The NCSBN Grant Program provides funding for scientific research projects that advance the science of nursing policy and regulation and build regulatory expertise worldwide. Research Priorities include, but are not limited to: (1) Outcome studies related to nursing regulation; (2) Nursing workforce; (3) Substance use disorders in nursing; (4) New technologies related to the profession; (5) Regulatory implications of practice innovations/new models of care delivery; (6) LPN, RN and APRN scope of practice; (7) Impact of policy on nursing
The Board will prioritize projects relating to interventions on day of birth – including prevention of stillborn deaths. Priority will be given to applications that: (1) Extend beyond local impact, demonstrating long- term practical value and inspiring advancements in other regions or countries; (2) Have innovative approaches to more efficient education and implementation; (3) Present collaborative initiatives relating to scale-up of proven concepts; (4) Take place in the Foundation’s focus countries: Tanzania, Ethiopia, Malawi, Bangladesh, India, and Nepal.
This supports practically oriented research within its stated 2025 strategy. Applications that relate to factors 2 and 3 of the Utstein Formula for Survival – improved efficiency of education or implementation, are particularly welcome. The Foundation supports projects advancing resuscitation, trauma, and maternal/newborn care.
Clinical Pilot and Feasibility Awards are offered to support projects involving human subjects that will develop and test new hypotheses and/or new methods (or those being applied to the problems of cystic fibrosis for the first time), and to support promising new investigators as they establish themselves in research areas relevant to cystic fibrosis. The intent of these awards is to enable investigators to collect sufficient preliminary data to determine the best strategies and methods for approaching a major question that ultimately will require assessment through a larger-scale research and/or multi-center, collaborative trial.
The goal of this NOFO is to encourage applications for studies that will enhance knowledge of mechanisms associated with neuropsychiatric symptoms (NPS) in persons with Alzheimer's disease (AD) or Alzheimer's disease- related dementias (ADRD). The findings are expected to advance mechanistic understanding of both biobehavioral and neurobiological pathways leading to NPS. Findings may also provide insight into novel therapeutic targets that can be advanced into interventions to treat and prevent the development of NPS in AD and/or ADRD.
This NOFO will broadly focus on closing the treatment gap for individuals with alcohol use disorder (AUD); within this focus, there are five major areas of emphasis: (1) increasing access to treatment for AUD, (2) making treatment for AUD more appealing, (3) examining cost structures and insurance systems, (4) conducting studies on dissemination and implementation of existing evidence-based approaches to treating AUD, and (5) reducing health disparities as a means of addressing the treatment gap in AUD for health disparity populations.
This call aims to study the health inequities and/or differences among under-studied PD communities, across the spectrum of ethnicity, ancestry, geography, socioeconomic conditions, and gender. Current research has established the following: (1) Diagnosis of PD among some under-studied communities is delayed; (2) Some under-studied communities are less likely to receive quality PD care; (3) Clinical trial enrollment among certain under-studied communities does not match their representation in the population; (4) Differences in clinical features, response to treatment, co-morbidities, prevalence, natural history, genetics and biomarkers among various under-studied PD populations have not been fully explored. Projects should address one of these four issues. Projects can be designed to detect inequities or differences, understand the reasons for the inequities or differences, or test an intervention to improve disparities.
This call supports research aimed at developing new insights into the pathophysiology, etiology and/or treatment of PD. Grant proposals can address research questions anywhere along the pipeline from basic science to rehabilitation-focused projects. APDA seeks to promote the entry of new investigators into the field of Parkinson research, as well as to support important new ideas in the field worthy of investigation.
The aim of the preclinical grants is to support innovative research that advances understanding of osteosarcoma biology, accelerate the development of new therapies, and ultimately improve patient survival and quality of life.
The Kyle Bryant Translational Research Award honors its namesake for his diligent efforts to aid the rapid translation of basic research discoveries into clinical applications. Eligible applications should focus on accelerating completion of translational stage activities necessary for advancement to clinical study of a therapeutic candidate or development of novel tools that address a critical bottleneck to the discovery or development of therapies. The specific aims must target one or more of the areas
The Keith Michael Andrus Cardiac Research Award aims to advance the understanding and treatment of cardiomyopathy associated with FA. Proposals for this award should focus on advancing understanding and/or treatment of the cardiac involvement in FA.
Proposals should focus on FA research that relies on collaboration among investigators from at least two different institutions. Special consideration will be given to proposals that involve international collaborations and bring new scientists to the FA community. The rationale for the collaboration needs to be convincing: it must clearly demonstrate that the research goals could not be achieved by just one of the participating groups and the synergy among the groups is essential for the success of the project.
The Childhood Cancer Therapeutic Catalyst accelerates the translation of discovery research into novel therapeutics. They invite applications for early drug discovery proposals from across all childhood cancer indications and modalities.
This scheme provides funding for established researchers/teams from any discipline who want to pursue bold/creative research ideas to deliver significant shifts in understanding related to human life, health and wellbeing.
This scheme provides funding for mid-career researchers from any discipline who have the potential to beinternational research leaders. They will develop their research capabilities, drive innovative programmes of work and deliver significant shifts in understanding related to human life, health and wellbeing.
This funding opportunity aims to support translational research that advances the clinical application of vascularization- and engraftment-focused strategies for islet replacement therapy in type 1 diabetes (T1D). Funded projects must address at least one of the following areas: 1) define vascular features that correlate with or predict graft function and long-term durability; 2) advance strategies to enhance vascular integration, perfusion and graft resilience at extrahepatic transplant sites; or 3) advance non- invasive technologies to monitor neovascularization, perfusion, vascular stability, and oxygenation in vivo.
This funding opportunity aims to support advancement of cutting-edge organoid- and organ on a chip-based disease models of Type I Diabetes (T1D). This initiative aims to validate and refine existing human-relevant in vitro models of T1D as tools for evaluation of pharmacological and genetic interventions with the goal of accelerating translation to clinical studies.
The call aims to address the following research priorities: ·National Collection- Documentation and Analysis · National Collection - Utilization and Outreach · The Economics of Heritage
The call aims to address the following research priorities: · Artificial Intelligence Assisted Healthcare · Artificial Intelligence Assisted Education · Artificial Intelligence Assisted Tourism
The call aims to address the following research priorities: - Enhancing Interoperability and Standardization - Advancing Data Management - Harnessing AI, Informatics, and Smart Technologies
The call aims to address the following research priorities: · AI-powered networks for secure, efficient, and adaptive telecommunications ·Exploring how 6G technologies can expand/enhance daily-life applications beyond the capabilities of 4G/5G · Advancing research on the challenges and solutions for seamless hybrid satellite/cellular/fiber networks ·Investigating quantum computing penetration and its implications for existing network architectures
The call aims to address the following research priorities: · Epidemiological Studies on Mental and Neurological Disorders in Qatar · Precision Mental and Neurological Health · Emerging Technologies for Mental and Neurological Health . Neuromodulation and Behavioral Therapies · Neurodevelopmental Research and Early Interventions
The call aims to address the following research priorities: · Artificial Intelligence, Informatics, and Technology Solutions in Precision Medicine · Disease Risk Stratification in Population Groups · Integration of Genomics and other Omics in Clinical Diagnostics · Pharmacogenomics from Discovery to Implementation
The call aims to address the following research priority: · Biodiversity
The call aims to address the following research priority: · Smart Integrated Disease Management (IDM) for Protected Vegetable Production · Resilient, Traceable, and Allergen-Safe Supply Chains for Specialty-Nutrition Foods · Agricultural policies and Agricultural Extension · Digital Agriculture and Food System Innovation
The aim is to support investigator-initiated trials to undertake (1) innovative clinical studies using novel agents, novel combination therapies, or immunotherapies with high potential for clinical activity in WM; and (2) studies that substantially improve quality of life and/or reduce prevalent disease complications. It is seeking distinctly novel advances and innovative approaches.
The IWMF seeks proposals to understand the mechanisms of Waldenstrom macroglobulinemia pathogenesis with a focus on (1) uncovering new features of WM biology and cellular vulnerabilities; (2) laboratory studies investigating mechanisms of WM relapse and therapy resistance; and (3) identifying novel, therapeutically exploitable targets that represent previously under-explored opportunities. Such foundational studies should be focused on translational potential and ultimately driven by the goals of improved patient outcomes and reduction or elimination of disease.
IWMF seeks to support correlative companion research studies within pharmaceutical and biotechnology company-sponsored trials for Waldenstrom macroglobulinemia patients that will be instrumental in determining the optimal use of new therapeutics under study. These projects leverage biological samples collected during trials to explore and validate biomarkers, mechanisms of response or resistance, or disease biology response to therapeutic intervention that will inform future clinical studies. Projects may include identifying genetic, proteomic, or immune markers that predict activity profiles, elucidating molecular mechanisms of resistance, TME profiling, MRD assessment, among others.
These grants aim to support research studies to (1) accelerate existing and additional IWMF Grants requiring further funding based on a novel, testable hypothesis that drives the additional funded research work toward translational and clinical applications (an Acceleration Grant); or (2) expand funding support for novel, translational mechanisms or targets, based on previous proof-of-concept work that may or may not have previous evidence of activity in B-cell malignancies (an Expansion Grant).
The aim of this grant is to provide support to talented young investigators with a background in hematology and/or oncology, encouraging them to either enter or continue WM research. A successful applicant’s academic program must have a formal teaching curriculum and mentoring from established investigators with a proven record of advancing relevant research in the B-cell malignancy or plasma cell malignancy field.
The Foundation for Prader-Willi Research (FPWR) is dedicated to supporting research to advance the understanding and treatment of Prader-Willi syndrome (PWS). Briefly, funding priority areas include: (1) Genotype to phenotype: understanding PWS genetics / how loss of PWS-critical region genes leads to the phenotype, (2) Neurobiology of hunger / feeding behavior and metabolism in PWS, (3) Neurobiology of cognition, maladaptive behavior, and mental health in PWS, (4) Clinical care research: evaluation of existing drugs and interventions to improve the significant clinical concerns in PWS and (5) Therapeutics development for PWS- Genetic therapies; novel or repurposed pharmaceuticals; and devices
The aim of this RFP is to further develop and validate established biomarkers for which there is a clear clinical need in Alzheimer's disease and related dementias. This RFP prioritizes biomarkers with a defined context of use, a clear advantage over other relevant biomarkers, and a path to commercialization and/or clinical use. Specifically, this RFP focuses on: (1) Developing novel PET ligands for clinical trials, (2) Supporting novel CSF biomarkers, (3) Validating innovative MRI approaches in larger cohorts and (4) Developing novel measures of functional activity such as EEG
This scheme provides funding for early-career researchers from any discipline who are ready to develop their research identity. Through innovative projects, they will deliver shifts in understanding related to human life, health and wellbeing. By the end of the award, they will be ready to lead their own independent research programme.
The purpose of this NOFO is to announce support for meritorious research projects that address research questions relevant to human dental, oral, or craniofacial (DOC) biology, and diseases and conditions, through analysis of existing and publicly available genomic data, with or without other types of complementary data, using statistical and computational approaches. Projects aimed at understanding oral health disparities to inform strategies for improving health for all individuals are a priority. Projects focused on investigating and/or characterizing human biological pathways to inform identification of intervention targets or defining the pathogenicity of known genetic variants are encouraged.
The purpose of this notice of funding opportunity (NOFO) is to support efficient and innovative natural history studies that advance medical product development in rare diseases/conditions with unmet needs. Through the support of natural history studies with high quality and interpretable data elements, FDA expects to address critical knowledge gaps, remove major barriers to progress in the field, exert a significant and broad impact on a specific rare disease or multiple rare diseases with similar pathophysiology, and facilitate rare disease product development.
This grant supports early-career investigators of exceptional creativity who propose highly innovative research projects with the potential to impact broad, essential areas of leukemia research. For the program to support the best and brightest minds, applications are sought from investigators who reflect the full diversity of the research workforce and represent diverse backgrounds, institutions, and geographic locations.
The Therapeutic Catalyst accelerates the translation of laboratory discoveries into novel cancer therapeutics. This scheme aims to de-risk early projects to facilitate further drug discovery research, funding, or partnering. They are seeking projects with strong therapeutic potential to deliver patient benefit. They invite applications for early drug discovery proposals from across all cancer indications and modalities.
The NPF is seeking grant applications that encourage the advancement of innovative research into psoriasis and psoriatic arthritis. Translational Research Grants fund research projects that focus on the rapid translation of basic scientific discoveries into clinical applications with a clear benefit for patients with psoriatic disease. Review of projects prioritizes applications with a thoughtful perspective of the translational pathway that will be required to advance the proposed aims towards clinical reality. Commitments to interinstitutional or interdisciplinary research are emphasized.
The NPF is seeking grant applications that encourage the advancement of innovative research into psoriatic disease and related comorbidities. Discovery Grants fund researchers to explore preliminary ideas and conduct proof-of-concept experiments. Review of projects prioritizes meaningful collaborations that offer the potential to bring significant new lines of inquiry to understanding root causes and potential cures for psoriatic disease.
The award’s goal is to help advance junior clinical research scientists in their professional endeavors to cure retinal degenerative disease by: (1) facilitating advances in laboratory and clinical research; (2) elucidating the mechanism for the cause and pathogenesis of retinal degenerative diseases; (3) developing innovative strategies to prevent, treat and cure these diseases.
ATF-BSI welcomes proposals to investigate sarcoidosis regardless of organ system. The scientific focus of ATF- BSI proposals should address one or more of the suggested focus areas.
The CRI Lloyd J. Old STAR Program — Scientists TAking Risks — provides long-term, flexible funding to mid-career scientists, giving them the freedom to pursue high-risk, high-reward research at the leading edge of cancer immunotherapy.
IFCAH aims to develop better ways to treat CAH (Congenital Adrenal Hyperplasia), allowing people to live better, healthier lives. Specific goals are available at the link below.
This grant provides three years of funding for hypothesis-driven research projects. The proposed research must represent an innovative approach to a major challenge in DIPG/DMG research. The funded projects must have the potential to lead to groundbreaking discoveries in the field and transform our understanding of the tumorigenesis process or our ability to treat or detect DIPG.
This grant provides three years of funding to a new DIPG/DMG investigator for hypothesis-driven research projects. The investigator may be either a newly independent researcher establishing a new DIPG/DMG research lab, or an established researcher who has not previously conducted brain tumor research.
This programme primarily funds preclinical and clinical research focused on slowing, stopping, or reversing Parkinson’s. For preclinical research, priority is given to projects that are likely to lead to clinical trials in people with Parkinson’s within 5 years. For clinical research, the funder supports clinical trials and sub-studies of trials in people with Parkinson’s. Research which is directed at symptomatic relief is not in remit.
Proposals are sought from academic or industry applicants for novel one-year pilot studies to investigate a mechanism underlying autoimmune disease, identify novel targets or mechanisms of autoimmune pathogenesis, validate therapeutic targets, or provide proof of concept for an innovative therapeutic strategy. Through the Insight Awards, Breakthrough T1D, Lupus Research Alliance, and the National MS Society seek to co-fund projects that will obtain more specific insights into the commonalities and differences of immune pathways that govern autoimmune disease processes and lay the groundwork for bringing together investigators from across autoimmune fields and disciplines. All project proposals should be relevant to multiple autoimmune diseases, two of which should be relevant to multiple sclerosis, systemic lupus erythematosus (or one of its manifestations), and/or type 1 diabetes. These projects should be designed to establish a proof of concept to a future expanded collaborative study and therefore should constitute “step-one” of an ambitious endeavor.
This funding opportunity aims to support the development of tolerance induction approaches for islet cell therapy that enables graft-specific immune protection without compromising natural immune defenses. This call is open to both central and peripheral tolerance induction strategies with prioritization given to technologies closest to clinical translation.
The Taking Flight Award seeks to promote the careers of early-career investigators to allow them to develop an independent research focus.
The purpose of these grants is to support clinical research at non-profit institutions worldwide focused on thefield of robotic-assisted surgery. Successful proposals will study important questions related to surgical care and patient outcomes. The Intuitive Foundation has identified key research areas of interest for the 2026- 2027 clinical grant programs. Principal Investigators are encouraged – although not required – to submit proposals that fall into one or more of the those areas.
The purpose of these grants is to support clinical research at non-profit institutions worldwide focused on the effect of robotic-assisted bronchoscopy in the clinical care of patients with pulmonary disease. Successful proposals will study important questions related to the impacts robotic-assisted bronchoscopy on disease diagnosis and or management or patient outcomes.
Applicants may propose projects under one of the following options: (1) Development of exceptionally low- cost nutrient ingredients (calcium, choline, DHA); (2) Development of a low-cost prenatal supplement (UNIMMAP MMS + 500 mg/day calcium); (3) Development of an advanced prenatal supplement (MMSplus: UNIMMAP MMS + 500 mg/day calcium + 100 mg/day nicotinamide + 450 mg/day choline + 200 mg/day DHA)
The purpose of these grants is to promote (1) New biomedical research into the etiology, genetic and molecular mechanisms and treatment of CHARGE syndrome, or (2) New research into clinical and medical diagnosis and treatment of CHARGE syndrome.
The purpose of the grant is to fund research that will accelerate the discovery of druggable oncogenic pathways and deliver cancer interception and cancer prevention therapeutics for RUNX1-FPD children and family members. It will lead to the development of therapies for patients with RUNX1-FPD that will either intercept the transition from a precancer state (clonal hematopoiesis) to MDS/AML or prevent blood cancer.
The aim is to develop continuous C-peptide monitoring (CCPM). Applications focused on early-stage development of sensor technologies, preclinical/feasibility studies and early-stage clinical evaluation of CCPM technologies will be considered. Letters of Intent (LOIs) are sought from academic and industry applicants with innovative approaches to develop CCPM technologies. Examples of research appropriate for this RFA include, but are not limited to: • Early-stage development of sensor technologies capable of continuous or high-frequency Cpeptide detection in biological fluids such as plasma or interstitial fluid. • Preclinical development and validation of CCPM systems. • Feasibility studies and early-stage clinical evaluation of CCPM technologies.
The purpose of this notice of funding opportunity (NOFO) is to invite applications proposing innovative analysis of existing social science, behavioral, administrative, and neuroimaging data to study the etiology and epidemiology of substance using behaviors (defined as alcohol, tobacco, prescription, and other substances) and related disorders, prevention of substance use and HIV, and health service utilization. This NOFO encourages the analyses of public use and other extant community-based or clinical datasets to their full potential in order to increase our knowledge of etiology, trajectories of substance using behaviors and their consequences, including morbidity and mortality, risk and resilience in the development of psychopathology, strategies to guide the development, testing, implementation, and delivery of high quality, effective and efficient services for the prevention and treatment of substance use disorder and HIV. Primary data collection is not allowed for applications in response to this NOFO.
This NOFO is intended to support novel environmental health research in which an unpredictable event or policy change provides a limited window of opportunity to collect human biological samples or environmental exposure data.
The Clinical Innovator provides funding for clinician- scientists aiming to launch innovative phase I/II or phase II. clinical studies using novel immunotherapies. In addition to the merits of the clinical and scientific rationale, studies will be selected based on their novelty, feasibility, and clinical impact.
CLIP supports pre-clinical and translational research that can be directly applied to optimizing cancer immunotherapy in the clinic. CRI CLIP Grants are awarded to qualified scientists exploring clinically relevant questions aimed at improving the effectiveness of cancer immunotherapies.
EREF has established three key research priorities. The decision comes in response to the urgent need for innovative solutions and a deeper understanding of these pressing environmental challenges. The three selected areas represent some of the most significant issues affecting resource management and the environment today. (1) Climate Change Impacts/Greenhouse Gas Emissions (2) Emerging Contaminants (3) Advancing Materials Circularity & Recycling
The AABB Foundation awards grants for investigator- initiated original research in all aspects of blood banking, transfusion medicine and biotherapies. Research content areas eligible for the grant program include the following: Immunology, Hematology, Immunohematology, Infectious Diseases, Biotherapies, and Patient Blood Management. Applications for research into innovative and new projects are a priority.
These support clinical or fundamental research projects focused on human gut microbiota related to health and disease. For the current round, project must focus on what perturbations may involve, but not exclusively, drugs, lifestyle factors, smoking, etc. The project should address mechanisms. Funding should not be used for a randomized controlled trial but can include the use/ analysis of samples collected from clinical trials.
The aim is to progress the understanding of the mechanisms that contribute to the variable clinical presentation of PTEN hamartoma tumour syndrome (PHTS). Research proposals should focus on one of the following aims: (1) Explore opportunities to identify and/or undertake preliminary validation of biomarkers for PHTS that could predict symptom onset, occurrence, or progression/severity of symptoms at the individual level. (2) Elucidate the mechanisms of clinical heterogeneity that may include assessment of how different PTEN variants and other genetic, molecular, or cellular mechanisms contribute to and are associated with the clinical spectrum associated with PHTS.
Pfizer and the CanAge are collaborating to offer a new grant opportunity seeking grant proposals for programs that seek to explore innovative approaches to persistent challenges impacting older adults living with rare diseases, including, but not limited to: • Accelerating time to diagnosis by increasing understanding of the symptoms (including the distinctions between ageing and illness) through enhanced clinical awareness and integration of genetic testing to identify underlying conditions earlier • Supporting development of National Action Plans on Rare Disease (RD) to including solutions for the specific challenges faced by older adults and communities ageing with RD • Gathering exisiting evidence to support advocacy for closing heatlhcare gaps and drive policy change
This program supports an innovative and collaborative group of researchers working together to improve our understanding of the biological mechanisms that underlie bipolar disorder. BD2 will fund teams of multidisciplinary scientists to develop targeted and groundbreaking research applications that will examine the genetic, molecular, cellular, circuit, and/or behavioral mechanisms of bipolar disorder.
This scheme provides funding for mid-career researchers from any discipline who have the potential to be international research leaders. They will develop their research capabilities, drive innovative programmes of work and deliver significant shifts in understanding related to human life, health and wellbeing.
The MDx Impact Grants aim to unlock the potential of PCR to democratise access to accurate diagnostic tests that improve patient outcomes. The goal is to develop tests that address unmet clinical needs. The programme provides researchers with access to Seegene’s syndromic PCR technology and development grants to perform clinical studies.
These grants are intended to facilitate research that will contribute to the development of new therapies or therapeutic strategies to treat CF, with an emphasis on advancing CFTR gene repair and replacement approaches. Collaborations that bring new investigators and technologies into the CF research community will be given highest priority. Proposals must include preliminary data to justify support from the Cystic Fibrosis Foundation.
The Well-Being in FTD Pilot Grant supports research to improve the well-being of persons diagnosed, families, and caregivers and to improve access to equitable, high- quality diagnosis, care, support, and research participation options. Please refer to the link below for examples of suitable research topics.
The aim is to support innovative research that advances the clinical translation of biomaterial-based immune- isolation strategies for islet cell replacement therapy in T1D. Preference will be given to proposals that: Use GMP-compatible biomaterials to enhance clinical relevance, Include benchmarking against biomaterials/devices with prior clinical testing, Use large animal models and NHPs, Involve collaborations between teams that have tested devices in preclinical models and can compile data towards better mechanistic understanding of the FBR or Build on previous clinical studies and/or explanted devices to elucidate mechanisms of human FBR
This award provides seed funding to address the gap between technology development and clinical application of cancer immunotherapies. These grants aim to encourage collaboration between technology developers and clinical cancer immunologists and to generate the proof-of-principle of a novel platform technology in bioinformatics, ex vivo or in silico modeling systems, immunological or tumor profiling instrumentation, methods, reagents and assays, or other relevant technologies that can enable clinician scientists to generate deeper insights into the mechanisms of action of effective or ineffective cancer immunotherapie
Grants awarded to investigators at or below the level of assistant professor. These grants must allocate a specified amount of their award for an established researcher to mentor the Early Career Researcher. AFSP is available to assist you in identifying a suitable mentor.
Awarded to investigators at any level, these grants provide seed funding for new projects that have the potential to lead to larger investigations. These grants typically entail feasibility studies rather than hypothesis- driven research. Examples include manual development and new biomarker development.
Applications addressing the priorities set out by the National Action Alliance for Suicide Prevention’s Research.Prioritization Task Force are encouraged. Priority area research applications are reviewed along with the general pool of grant applications, with priority given to strong grants in the designated areas.
Grants awarded to investigators at the level of associate professor or higher with an established record of research and publications.
The purpose of this Notice of Funding Opportunity (NOFO) is to support and facilitate multidisciplinary approaches towards the development of new and/or improved contraceptive methods for both men and women through the formation of a Contraceptive Development Research Center. This NOFO also allows the inclusion of translational studies to facilitate the pre- clinical to clinical transition and increase the likelihood of clinical success.
The purpose of this NOFO is to solicit research applications focused on preclinical development of lead candidate vaccines to prevent Mycobacterium tuberculosis infection and/or disease, and to increase the clinical pipeline of viable vaccine candidates.
The World Cancer Research Fund International invites applications for its regular grant programme. The aim of the WCRF Regular Grant Programme is to support innovative and original research into the role of diet, nutrition and physical activity in either Cancer Prevention or Cancer Survivorship.
The IETF is requesting proposals for grants addressing the etiology and pathogenesis of essential tremor. Concise, clearly written proposals that are hypothesis- driven have the best chance of being funded. Applications should focus on studies achieving one or more of the following goals: 1) A better understanding of the underlying pathophysiology of ET, including independent validation of previous findings. 2) A better understanding of the etiology of ET 3) Development or further validation of animal models of ET
Researchers of any country are invited to apply for research grants covering ‘basic science’ research that can help support a better understanding of Angelman Syndrome and eventually lead to new treatments tackling the genetic and molecular processes underlying the condition.
GBS/CIDP Foundation International invites letters of intent for its Discovery Award. These support researchers who are committed to learning more about Guillain-Barre syndrome, chronic inflammatory demyelinating polyneuropathy and variants.
Proposals should address key outstanding questions and have the potential to lead to a challenge or a change in the current paradigm or conventional wisdom and/or lead to a groundbreaking discovery. Preliminary data is not required in the proposal, but the underlying concept, premise or hypothesis must be plausible and testable, and the proposal must be focused with a well-defined goal that is achievable within the timeframe and amount of the award.
The objective of this grant is to to explore an innovative concept that has applicability to improving human health. Examples could include fundamental research, clinical research, diagnostic tests, biomarkers, biomedical engineering advances, and imaging advances.
This grant program is designed to support investigators early in their career to derive preliminary data in a key concept area that has high potential to lead to extended funding from NIH, EU, etc.
The purpose of this Notice of Funding Opportunity (FOA) is to enhance mechanistic and epidemiologic investigations addressing the roles of co-infection and cancer to shed light on presently unestablished pathways in carcinogenesis that may inform prevention and treatment strategies for infection-related cancers. Preference will be given to investigations of co-infections with known oncogenic agents (excluding human immunodeficiency virus [HIV]) and of co-infections that engender novel opportunities for prevention and treatment.
The Disease Model Award is designed to advance the field by developing and validating innovative models to support the scientific community in accelerating discovery. Applications must focus on disease models and their validation. Proposals primarily centered on therapeutic development research are out of scope for this program and will not be reviewed. The goal is to develop, validate, or utilize non-rodent disease models (in silico, in vitro, or in vivo) for therapeutic development for IRD and dAMD.
The Polio Research Committee is calling for research proposals supporting the Polio Endgame Strategy 2022- 2026. Research proposals supporting the strategic plan may be submitted to the Committee for review and funding. Preference will be given to proposals developed by GPEI partner agencies and their research collaborators. However, other institutions may also submit proposals if they address their research priorities.
This award is open to scientists with a PhD or MD, regardless of nationality or location. The Parkinson's Foundation Impact Awards are intended for researchers both established and new to the field of PD.
The purpose of this NOFO is to encourage applications to phenotype and/or perform research on embryonic lethal knockout (KO) mouse strains being generated through the International Mouse Phenotyping Consortium (IMPC) of which the NIH Knockout Mouse Phenotyping Program (KOMP2) is a member. The mission of IMPC is to generate a comprehensive catalogue of mammalian gene function that will provide the foundation for functional analyses of human genetic variation.
Cure SMA encourages applications on novel research that will enhance the understanding of SMA disease pathology at the molecular, cellular, and biochemical level; generate key reagents and tools to facilitate drug development and clinical trials; and identify new therapeutic strategies for SMA. Particular interests exist in understanding mechanisms underlying the pathology of disease and/or identifying drug targets synergistic with SMN-upregulating therapeutics for use in older/symptomatic patients.
Well-suited applications must propose the development of technologies that offer the potential to accelerate and/or enhance research in the areas of cancer biology, early detection and screening, clinical diagnosis, treatment, cancer control, epidemiology, and/or address issues associated with cancer health disparities. Technologies proposed for development may be intended to have widespread applicability but must be focused on improving molecular and/or cellular characterizations of cancer biology.
The National Cancer Institute (NCI) invites grant applications proposing exploratory research projects focused on further development and validation of emerging technologies offering novel capabilities for targeting, probing, or assessing molecular and cellular features of cancer biology for basic, clinical, or epidemiological cancer research.
This NOFO solicits applications for support of exploratory/developmental studies aimed at accelerating progress toward understanding, preventing or treating Guillain Barre Syndrome (GBS) and/or Chronic Inflammatory Demyelinating Polyneuropathy (CIDP). Innovative studies of disease mechanisms, susceptibility factors, model systems, biomarkers and treatments are encouraged.
The fiscal year 2025 (FY25) Prostate Cancer Research Program (PCRP) Idea Development Award (IDA) supports new ideas that represent innovative approaches to prostate cancer research and have the potential to make an important contribution to the PCRP mission. All applications are required to address one or more of the FY25 PCRP Overarching Challenges.
The fiscal year 2025 (FY25) Prostate Cancer Research Program (PCRP) Clinical Consortium Award (CCA) provides support to develop, maintain, and enhance the necessary collaborations and resources to rapidly execute phase 2 and/or phase 2-linked phase 1 (phase1/2) prostate cancer clinical trials. The primary intent of the PCRP Clinical Consortium Award is to combine the efforts of leading investigators across multiple institutions to expedite the clinical advancement of novel therapeutic interventions in prostate cancer to decrease the impact of the disease.
Research Grant Awards are intended for established, experienced, independent investigators affiliated with a research or academic institution whose proposed projects investigate hypotheses directly related to Dravet syndrome. Proposals are scored according to NIH guidelines based on the quality of preliminary data, research design, feasibility, investigator’s qualifications, and overall impact. Grants are awarded for $250,000 over 2 years (beginning January 1 of each year), with indirect costs not to exceed 10% of the award.
Transformational Science Grants are intended for established, experienced, independent investigators affiliated with a research or academic institution whose proposed projects have substantial preliminary data, investigate hypotheses directly related to Dravet syndrome, and have potential to significantly impact the field of research.
The ultimate goal of this grant program is to drive research that will eliminate the delivery of pre-term babies as an intervention for severe preeclampsia, HELLP syndrome, and related hypertensive disorders of pregnancy.
Vision Grants are intended to provide initial funding for novel, innovative research by promising young investigators that will advance progress towards detection, prevention, or treatment of preeclampsia, HELLP syndrome, and other hypertensive disorders of pregnancy. Post-doctoral, Clinical Fellows, or Early Stage Investigators only are eligible to apply.
This award is intended to fuel early-stage ideas by supporting emerging investigators in testing new concepts, piloting experiments or exploring novel data analyses.
This award is intended to promote research in topic areas of special interest that relate to NEA’s advancement of our overall research priorities for eczema. The availability of this grant category will be determined on an annual basis; topics of special interest may vary. For 2025, specific areas of research interest include: patient-centered outcomes research.
This award provides funding support for experienced researchers with recognized productivity — either within or outside the eczema field — to conduct highly innovative, cutting-edge investigations related to eczema. Data from this award can then be used to seek additional, larger-scale funding from the National Institutes of Health (NIH) or other funding entities to build on these discoveries.
The Childhood Eczema Challenge Grant is intended to stimulate early and mid-career scientists as they seek to build and sustain careers as research investigators and future thought leaders within this critical field of study
The purpose of this RFP is to solicit programs that have identified a resource limitation within their healthcare organization that impacts establishment of a holistic and sustainable antimicrobial stewardship (AMS) program...
Pfizer invites Health Care Organizations based in the countries listed in the Geographic Scope to submit quality improvement (QI) initiatives focused on improving the outpatient management of COVID-19 patients by providing leadership...
Pfizer Global Medical Grants (GMG) supports the global healthcare community’s independent initiatives (e.g., research, quality improvement or education) to improve patient outcomes in areas of unmet medical need that are aligned with Pfizer’s medical and/or scientific strategies.
The intent of this RFP is to support independent education initiatives for healthcare professionals involved in the treatment of patients with locally advanced or metastatic urothelial carcinoma...
Through this Funding Opportunity Announcement (FOA), the National Cancer Institute (NCI) invites applications for Cancer Control Research in Persistent Poverty Areas...
The Food and Drug Administration (FDA) protects the public health by ensuring that pharmaceutical drug products intended to be marketed in the United States are safe and effective for their intended use...
This Funding Opportunity Announcement (FOA) will support UG3/UH3 phased, cooperative agreement research applications to plan and implement effective interventions or programs to prevent, reduce...
With 10 million cases and 1.5 million deaths reported every year, Tuberculosis (TB) is one of the leading global infectious disease killers. Among new TB cases, an estimated 4.1% have multidrug-resistant...
This Funding Opportunity Announcement (FOA) invites applications to participate in the Immune Drivers of Autoimmune Disease (IDAD) cooperative research program, which will focus on defining the immunologic states and dynamics that drive autoimmune disease...
To stimulate research, the EACTS has instituted prizes for the best manuscripts on topics of clinical or experimental research in the fields of Thoracic Surgery, Cardiac Surgery, and Congenital Heart Disease presented by young investigators at the Annual Meeting...
Notice of special interest – accelerating progress in celiac disease research funding opportunity. This supports research on the etiology and pathogenesis of celiac disease, identification of therapeutic targets, and development of preventative or disease ameliorating therapies and strategies. Each institute has its own research priorities.
The Simons Foundation, under its Autism Research Initiative, invites applications for its analysis of post-mortem brain tissue from the Autism Brain Net collection funding opportunity...
The CREID Network Pilot Research Program supports, trains, and mentors the next generation of emerging infectious disease researchers. This program will help develop capacity for emerging infectious disease research around the world through the performance of scientific research projects.
The Eunice Kennedy Shriver National Institute of Child Health and Human Development invites applications for its elucidating the role of nutrition in care and development of preterm infants (R01 clinical trial optional) funding opportunity. This supports research addressing priority...
JDRF invites letters of intent for its novel strategies to enhance beta cell replacement therapies for type 1 diabetes (T1D) funding opportunity. This supports preclinical and clinical studies from academic or industry applicants with innovative and incremental immune...
To make grants to fund relevant nutritional research. To support programs for the education and training of mothers during pregnancy and after the birth of their children, so that good nutritional habits can be formed at an early age. To assist in the training of persons to work as educators and demonstrators of good nutritional practices. To encourage the...
This encourages innovative, collaborative research projects between US and low- and middle-income country scientists, on brain and other nervous system function and disorders throughout life, relevant to LMICs. This includes neurological, mental, behavioural...
Pfizer invites letters of intent for its ASPIRE global obesity grant. This supports basic science, preclinical research and clinical research, animal experimentation related to human biology and physiological, cellular, molecular and translational research regarding obesity.
The purpose of the Fogarty Emerging Global Leader Award is to provide research support and protected time (three to five years) to an early career research scientist from a low- or middle-income country (LMIC) who holds a junior faculty position at an LMIC academic or research institution, as defined by the World Bank...
The Patient-Centered Outcomes Research Institute invites letters of intent for its call on comparative effectiveness of multimodal interventions to prevent osteoporotic fractures. This supports comparative effectiveness research projects that focus on multimodal ...
The Wings for Life invites executive summaries for its project research grants. These support basic or clinical research projects related to spinal cord injury with the perspective to improve outcomes. Projects may be in the following areas: • basic research projects – nerve regeneration and plasticity, neuronal and glial protection, functional deficits induced by...
These support research that accelerate the understanding of the biological mechanisms underlying Alzheimer’s disease and related dementias as well as innovative approaches to better diagnose, prevent, or delay the progress of the disease. The awards are designed for researchers who have already generated some amount of preliminary data but are...
Strategic research agreements. These enable single or multiple investigators to address critical gaps and challenges and potential breakthroughs in type 1 diabetes research. Clinical trials may also be supported.
Healthcare professionals need to understand the latest scientific data in order to make evidence-based treatment decisions and provide optimal care for patients with ER+ HER2- metastatic breast cancer.
This supports the review and analysis of retrospective, local source surveillance of the pneumococcal disease burden or serotype distribution, whether in children or adults, as determined before, during or following the implementation of a pneumococcal...
Johannes Wenner prize. This supports research projects of society members in relation to the improvement of care and treatment of children with lung diseases.
Bright Focus provides research funds for U.S. domestic as well as international researchers pursuing pioneering research leading to greater understanding, prevention, and treatment of age-related macular degeneration.
R01 funding mechanism to support discrete, specified, and circumscribed projects on novel molecular imaging approaches to establish high-resolution mapping of biomolecules in brain cells and regions during the course of aging and Alzheimer’s disease (AD). This FOA...
Preclinical, clinical and outcomes research aimed at increasing medical knowledge in alopecia areata, atopic dermatitis or vitiligo.
The goals of this program are to support locally relevant research in critical areas of HIV-associated non-communicable diseases (NCDs) at Low- and Middle- Income Country (LMIC) Institutions, to enhance research capacity, and to build a network of researchers...
EFSD/Lilly exploring and applying new strategies in diabetes expand the program. This supports diabetes research projects on potential strategies that can be implemented in Europe and rolled out in low and middle-income countries to favor the improvement of quality of care for people living with diabetes.
This aims to contribute to the development of stronger and more inclusive movements advocating for sexual reproductive health and rights in sub-Saharan Africa, south Asia and Middle East and north Africa (MENA) region.
Staying healthy call. This supports projects that set out a credible pathway to contributing to staying healthy in a rapidly changing society.
The Children’s Tumor Foundation invites letters of intent for its drug discovery initiative registered reports award program. This supports early-stage testing of candidate drug therapies for the treatment of neurofibromatosis.
Research addressing the most intractable issues in paediatric cancer. Projects should fall under the following research themes: developmental origins of paediatric cancers; drugging currently undruggable paediatric cancers; developing novel immunotherapies; or discovery and development of novel paediatric cancer drug targets.
Research grants to stimulate innovative research in challenging areas of future importance. You may apply for more than one grant or submit your application for more than one focus topic: Drug Discovery, Real time testing and sensors, Nanoparticle for nucleic acid...
MPM oncology charitable foundation transformative cancer research grants. These support early- to mid-career researchers in undertaking paradigm-shifting cancer research that might not be funded through conventional channels.
Research projects on Down’s syndrome. Applications may cover fundamental, translational, epidemiological, clinical research, neurobiology and pharmacology, genetic, genomic, induced pluripotent stem cells, neuropsychology techniques or data analysis. Priority will be given to clinical research projects.
Closing knowledge gaps in transthyretin cardiomyopathy in emerging markets under its competitive grants program. This supports projects that focus on closing the knowledge gaps in transthyretin cardiomyopathy within Asia, Latin America, Africa, and Middle East. Projects should focus on: educating healthcare providers on the subject matter; creating strategies...
COVID-19 Epidemiology Research Projects that will be considered for Pfizer support should be focusing on SARS-CoV-2 Variants epidemiology, T-cell responses to SARS-CoV-2 – from natural infection or Paediatric COVID-19 epidemiology – in children and adolescents <16 years, characterization of disease burden and epidemiology.
IsDB-TWAS Joint Research & Technology Transfer Grant 2021: Quick-Response Research on COVID-19.This supports technologists and researchers from IsDB member countries in collaborating to address challenges directly and indirectly related to COVID-19.
John W Walsh translational research award supports research aimed at finding a cure for alpha-1 antitrypsin deficiency.
Appropriate immunization in patients with immune- mediated inflammatory conditions. This supports quality or process improvement projects, and medical education and patient awareness initiatives aimed at addressing the vaccination needs and gaps among patients...
Support research-training programs that focus on: - Major endemic or life-threatening emerging infectious diseases, Neglected tropical diseases, Infections that frequently occur as co-infections in HIV infected individuals or Infections associated with non- communicable disease conditions of public health importance in LMICs.
This opportunity fosters research in the areas of early OA and prevention of OA progression. Proposed studies need not relate specifically to sports injuries. Research priorities include: Investigating the pre-osteoarthritic joint; Examining prevention or treatment of posttraumatic OA; Determining the relationship between injury and OA; Enhancing clinical...
This supports research to improve the immediate care of children and adults with cystinosis and to develop a new understanding and treatment of cystinosis to help these patients in the future.
The Myositis Association has a competitive grant program for innovative pilot research into any type of immune- mediated myositis...
These support members of the organisation in conducting research relevant to inflammatory bowel disease. The aim is to fund two clinical and two basic science projects.
This supports projects that document, synthesise and disseminate evidence of capacities for international health regulation (2005) implementation, health security and health emergency preparedness, as well as supporting the collaborative development and advancement...
Projects that will be considered for Pfizer support will focus on improving the care of patients by addressing knowledge gaps in following areas. Grant proposals can address either Atrial Fibrillation (AF) or Venous Thromboembolism (VTE) or both areas...
Supports research focusing on osteoarthritis and chronic pain associated with osteoarthritis, as well as patient- centered standard of care and management. Research may include pain and function, the biopsychosocial aspects of the disease, the complexities, and challenges of care, and the future of osteoarthritis and osteoarthritis pain management. Programs...
This supports the development of cancer-relevant technologies suitable for use in low- and middle-income countries (LMICs). The aim is to adapt, apply and validate existing or emerging technologies into a new generation of user-friendly...
Three award opportunities from the European Association for Cardio-Thoracic Surgery that you may apply for.
Manuscripts on topics of clinical or experimental research in the fields of thoracic surgery, cardiac surgery and congenital heart disease, presented by young investigators at the association’s annual meeting.
This stimulates advanced clinical or experimental research in the field of thoracic aortic surgery by young investigators, as documented by a presentation during the annual meeting of the association.
The Dravet Syndrome Foundation invites applications for its research grants. These support research projects investigating hypotheses directly related to Dravet syndrome. The priority areas...
This recognizes a clinical and basic scientific research project within the field of neurodegenerative diseases and psychiatric disorders.
William E Paul distinguished innovator award in lupus and autoimmunity. This supports novel research into the fundamental causes of lupus to provide new directions toward a cure. Novel, hypothesis or discovery-driven proposals using clinically relevant models in lupus research are welcome. Proposals must aim to uncover the fundamental causes of lupus and...
HEALTHLINE and their reporter's teams are doing an outstanding job, particularly, in these difficult challenging existential times. Covid-19 pandemic is ravaging the world reaping lives without distinction between races, languages, nationalities, social level, faith, and religion. Thanks to HEALTHLINE for the great job they are offering to the community and for the daily updates spreading the right information and saving lives.
These enable members to undertake research activities and network among centers at an international level. Activities may include interactive educational events and clinical networks. Proposals relevant to the society’s activities, such as the validation of guidelines, or clinical networks for testing treatment regimes or disease management, are encouraged.
These support research that may lead the way to the cure or the improved therapeutic management of lymphoma. Basic, translational or clinical research on malignant lymphoma, malignant lymphoid neoplasia and related malignant blood diseases is supported.