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Award Data
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.
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TOPICAL PRODRUGS FOR THE TREATMENT OF PSORIASIS
SBC: MOLECULAR DESIGN INTERNATIONAL, INC. Topic: N/APSORIASIS IS A DISEASE THAT AFFECTS MILLIONS OF AMERICANS WITH CHRONIC RECURRENT EXACERBATIONS AND REMISSIONS THAT AREEMOTIONALLY AND PHYSICALLY DEBILITATING. SEVERAL TREATMENTSARE AVAILABLE, BUT IN MANY CASES THESE ARE INADEQUATE. THIS APPLICATION IS BASED ON THE PREMISE THAT TOPICAL ADMINISTRATION OF PRODRUGS SHOULD RESULT IN HIGH CONCENTRATIONS OF THE ACTIVE DRUG AT THE LESION SITE WITH LOWER C ...
SBIR Phase II 1991 Department of Health and Human Services -
TOPICAL PRODRUGS FOR THE TREATMENT OF PSORIASIS
SBC: MOLECULAR DESIGN INTERNATIONAL, INC. Topic: N/AN/A
SBIR Phase I 1988 Department of Health and Human Services -
TOPICAL PRODRUGS FOR TREATMENT OF ACNE AND SKIN DISEASES
SBC: MOLECULAR DESIGN INTERNATIONAL, INC. Topic: N/ATHE LONG-TERM OBJECTIVE OF THIS PROJECT IS TO DEVELOP A COMMERCIAL PRODUCT FOR THE TOPICAL TREATMENT OF ACNE AND SKIN DISEASES. THE SPECIFIC AIM OF THE PROPOSAL IS TO INVENT A PRODRUG THAT CAN BE USED EFFECTIVELY AND SAFELY FOR THE TOPICAL TREATMENT OF ACNE. SINCE ISOTRETINOIN (13-CIS-RETINOIC ACID, ACCUTANE-ROCHE) ADMINISTERED ORALLY CAUSES BIRTH DEFECTS AND APPLIED TOPICALLY IS IRRITATING, WE HA ...
SBIR Phase II 1987 Department of Health and Human Services -
TOPICAL PRODRUGS FOR TREATMENT OF ACNE AND SKIN DISEASES
SBC: MOLECULAR DESIGN INTERNATIONAL, INC. Topic: N/AN/A
SBIR Phase I 1985 Department of Health and Human Services -
Topical proprietary biologic to treat oral mucositis
SBC: Allander Biotechnologies Topic: NIDCRSummary Oral mucositisa severe oral ulcerationis a common toxic effect of radioor chemoradio therapy and a limiting factor to using the maximum dose of radiation for effective cancer treatmentAt leastand up toof cancer patients treated with standard chemotherapy regimens or upper body radiation develop oral mucositisIntensity modulated RTIMRTlessens chronic side effectsbut not the acute toxicity s ...
SBIR Phase II 2017 Department of Health and Human ServicesNational Institutes of Health -
Topical Protector Against Chemo/Radiotherapy
SBC: Procertus Biopharm, Inc. Topic: N/ADESCRIPTION: (Verbatim) A National Institutes of Health study has indicated that "hair loss during cancer chemotherapy is probably the most troubling aspect of cancer treatment, it is psychologically debilitating and adds to the overall trauma of the cancer diagnosis and . treatment." We have developed a topically applied pharmaceutical, called ProDermaCel, that h ...
SBIR Phase I 2001 Department of Health and Human ServicesNational Institutes of Health -
Topical Retinoids for Chemoprevention of Melanoma
SBC: IVREA, INC. Topic: N/ADESCRIPTION (provided by applicant): Malignant melanoma's incidence is increasing by 2.7% annually even as most other cancers are experiencing a decline in incidence. The long-term objective of this project is to commercialize a topical formulation containing retinoic acid (ATRA) for subjects with dysplastic nevi at a higher risk of developing malignant melanoma. However, ATRA is highly irritating ...
SBIR Phase II 2003 Department of Health and Human ServicesNational Institutes of Health -
Topical Retinoids for Chemoprevention of Melanoma
SBC: IVREA, INC. Topic: N/ADESCRIPTION (provided by applicant): Malignant melanoma's incidence is increasing by 2.7% annually even as most other cancers are experiencing a decline in incidence. The long-term objective of this project is to commercialize a topical formulation containing retinoic acid (ATRA) for subjects with dysplastic nevi at a higher risk of developing malignant melanoma. However, ATRA is highly irritating ...
SBIR Phase I 2003 Department of Health and Human ServicesNational Institutes of Health -
TOPICAL SALICYLANILIDES TO TREAT DIABETIC FOOT ULCER
SBC: OMNIPHARM RESEARCH INTERNATIONAL INC. Topic: N/AThe goal of this program is to develop a topical pharmaceutical formulation containing an optimized drug candidate from the 5-(n-substituted)salicylanilide class of patented, Lipophilic, Antimicrobial, Anti-inflammatory Drugs (LAADs) for the treatment of Diabetic Foot Ulcer (DFU). The 5-(n-substituted)salicylanilides are unique in that they potently inhibit the growth of several Gram-positive and ...
SBIR Phase I 2002 Department of Health and Human ServicesNational Institutes of Health -
Topical selective T-type blockers for the treatment of neuropathic pain
SBC: DERMAXON LLC Topic: 105Project SummaryAbstract Paclitaxel is widely used throughout the field of oncology with indications for the treatment of a number of solid tumorsThe most commonly reported neurotoxic effect of paclitaxel is peripheral sensory neuropathy which often limits the dose and frequency of paclitaxel treatmentNeuropathic pain management is currently aimed only at reducing symptoms and treatment of chronic ...
STTR Phase I 2018 Department of Health and Human ServicesNational Institutes of Health