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The Award database is continually updated throughout the year. As a result, data for FY24 is not expected to be complete until March, 2025.

Download all SBIR.gov award data either with award abstracts (290MB) or without award abstracts (65MB). A data dictionary and additional information is located on the Data Resource Page. Files are refreshed monthly.

The SBIR.gov award data files now contain the required fields to calculate award timeliness for individual awards or for an agency or branch. Additional information on calculating award timeliness is available on the Data Resource Page.

  1. Phase Gratings for ORNL HFIR and SNS Neutron Imaging Interferometers

    SBC: REFINED IMAGING, LLC            Topic: 12a

    The Oak Ridge National Laboratory (ORNL) Neutron Imaging Facility will build a Talbot- Lau interferometer for advanced imaging projects, including inspection of additive manufactured components- This SBIR seeks to enhance the ORNL interferometer with novel optics, enabling the interferometer to operate in both Talbot-Lau and the recently invented far-field mode- Dual-mode operation is an ORNL goal ...

    SBIR Phase I 2018 Department of Energy
  2. 4-Demethyl-4-cholesteryloxycarbonylpenclomedine (DM-CHOC-PEN: A Phase II Clinical Trial in Adolescents/Young Adults (AYA)with CNS Malignancies

    SBC: DEKK-TEC INC            Topic: 102

    Abstract – The goal of this Phase II clinical trial application will be to evaluate 4-demethyl-4- cholesteryloxycarbonylpenclomedine (DM-CHOC-PEN) as anticancer therapy for adolescents and young adults (AYA) with cancer involving the brain in a Phase II clinical trial. DM-CHOC-PEN (Fig. 1) is a polychlorinated pyridine cholesteryl carbonate (Fig. 1) that is lipophilic, electrically neural, is ab ...

    SBIR Phase II 2018 Department of Health and Human ServicesNational Institutes of Health
  3. Double Chimeric Peptide Vaccine Feasible for Human Use that Protects against Disseminated Candidiasis caused by medically important Candida species

    SBC: Autoimmune Technologies, LLC            Topic: NIAID

    PROJECT ABSTRACT The goal of this Phase I STTR proposal is to develop and establish preclinical proof of concept for the first double chimeric peptide vaccine feasible for human use that protects against disseminated candidiasisDisseminated candidiasis is the third leading cause of nosocomial bloodstream infections in the USwithcases per year and associated healthcare costs of $billionanddespite t ...

    STTR Phase I 2018 Department of Health and Human ServicesNational Institutes of Health
  4. Development of 3D Rat Nerve-on-a-Chip Model for Chemical Toxicity Screening

    SBC: AXOSIM, INC.            Topic: NIEHS

    Abstract Development ofD organotypic cellular models utilizing animal cells is important for the validation of these systems by direct comparison to animal dataA few organizations have been successful in providing such assays for various organ systemsHoweverdevelopment of peripheral nerve assays is laggingCommonly used peripheral neural culture preparations are not predictive of clinical toxicityp ...

    SBIR Phase I 2018 Department of Health and Human ServicesNational Institutes of Health
  5. Evaluation of oral oleocanthal to prevent and/or treat Alzheimer's disease and related dementias

    SBC: Oleolive, Inc.            Topic: NIA

    PROJECT SUMMARY Alzheimer s diseaseADis a progressive neurodegenerative disorder of the elderly that afflicts aboutmillion patients globally and overmillion Americans in the USDespite the considerable research effort to preventtreator cure the diseaseeffective strategies remain lackingThe accumulation of amyloidAin the brain blood vessels can result in the development of cerebral amyloid angiopath ...

    SBIR Phase I 2018 Department of Health and Human ServicesNational Institutes of Health
  6. IND-Enabling Studies of ZB716, an Orally Bioavailable SERD

    SBC: Zenopharm, LLC            Topic: 102

    Project Summary Fulvestrant is the only FDA approved selective estrogen receptor downregulatorSERDindicated for advanced metastatic breast cancer that has progressed after or during tamoxifen or aromatase inhibitorAItreatmentIn July and Augustfulvestrant was approved as a first line endocrine agent for breast cancer patients by the European Medicines AgencyEMAand US FDArespectivelyHoweverthe drug ...

    SBIR Phase II 2018 Department of Health and Human ServicesNational Institutes of Health
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