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Source: IRS e-Filed Form 990 (from the IRS e-File system), Tax Year 2024
Total Revenue
▼$333.9K
Program Spending
80%
of total expenses go to program services
Total Contributions
$168.3K
Total Expenses
▼$360.3K
Total Assets
$288K
Total Liabilities
▼$4,378
Net Assets
$283.6K
Officer Compensation
→$171K
Other Salaries
N/A
Investment Income
$0
Fundraising
▼N/A
Source: USAspending.gov · Searched by organization name
Total Federal Funding
$9.3M
Awards Found
10
| Awarding Agency | Description | Amount | Fiscal Year | Period |
|---|---|---|---|---|
| Department of Energy | TAS::89 0227::TAS RECOVERY; NEW PHASE I SBIR: RECOVERY ACT; TITLE: RECOVERY ACT - A VARIABLE-GEOMETRY OSCILLATING WAVE SURGE CONVERTER PADDLE FOR MAX | $2.1M | FY2010 | Feb 2010 – Feb 2013 |
| Department of Health and Human Services | TARGETING MACROPHAGES TO TREAT SOFT TISSUE SARCOMAS - PROJECT SUMMARY SOFT TISSUES SARCOMAS (STS) IS A BROAD TERM FOR MULTIPLE SUBTYPES OF CANCER THAT START IN SOFT TISSUES. MOST STS ARE TREATED IN THE SAME WAY IN THE CLINIC REGARDLESS OF THE SUBTYPE. STS ENCOMPASSES OVER 50 HISTOLOGIC AND MOLECULAR SUBTYPES, WITH EACH DISPLAYING VARIABLE CLINICAL BEHAVIOR. THERE IS CURRENTLY NO UNIFYING TREATMENT FOR STS SUBTYPES BEYOND SURGERY, CHEMOTHERAPY, AND RADIATION. RESOLUTE SCIENCE INC. IS DEVELOPING NOVEL STS THERAPY BY USING TAMS TO PROCESS AND DELIVER ANTI-CANCER AGENTS TO SOLID TUMORS. TARGETING TAMS TO KILL THE ASSOCIATED CANCER HAS THE ADVANTAGE OF BEING TUMOR-AGNOSTIC COMPARED TO THAT OF TARGETING A SPECIFIC CANCER CELL RECEPTOR. THIS APPROACH BYPASSES CONCERNS OF TUMOR HETEROGENEITY AND EVOLVED RESISTANCE ASSOCIATED WITH THERAPEUTICS THAT TARGET SPECIFIC PROPERTIES OF EACH CANCER TYPE. OUR LEAD THERAPEUTIC, RS-5, IS WELL-TOLERATED AND DEMONSTRATED STRONG ANTI-CANCER EFFICACY ACROSS MULTIPLE MURINE SARCOMA TUMOR MODELS, INCLUDING THE SUBCUTANEOUS (SC) AND INTRACRANIAL (IC) HT1080 SARCOMA CELL LINE MODEL AND A DOXORUBICIN-RESISTANT PATIENT DERIVED XENOGRAFT (PDX) SARCOMA MODEL. RESOLUTE’S MODULAR DRUG DESIGN ALLOWS FOR STRAIGHTFORWARD CHEMICAL SUBSTITUTIONS OF LIGAND, BACKBONE, LINKER, AND PAYLOADS. FINALLY, THE COST OF COMMERCIAL MANUFACTURING WILL BE SIGNIFICANTLY LOWER THAN THAT OF ANTIBODIES AND ANTIBODY-DRUG CONJUGATES (ADCS) WHICH COULD SIGNIFICANTLY REDUCE THE PRICE OF THIS CANCER TREATMENT FOR PATIENTS AND INSURERS. THE OVERALL GOAL OF THE FAST-TRACK PROGRAM IS TO CONDUCT STUDIES THAT FURTHER SHOW THE EFFICACY OF RESOLUTE’S PLATFORM MOLECULE AS THERAPY FOR DIFFERENT STS SUBTYPES AND PERFORM PRE-INVESTIGATIONAL NEW DRUG (IND) AND IND-ENABLING STUDIES. OUR PHASE I GOAL FOR THIS SBIR FAST-TRACK PROPOSAL IS TO VALIDATE THE CHOICE OF ONE SUBTYPE OF STS, UNDIFFERENTIATED PLEOMORPHIC SARCOMA (UPS) AS AN INITIAL CLINICAL INDICATION FOR RS-5. THE MEASURE OF SUCCESS TO ADVANCE TO PHASE II IS 1) ESTABLISH DOSE RESPONSE OF RS-5 IN A DOXORUBICIN-RESISTANT UPS MODEL, 2) ESTABLISH ANTI-CANCER EFFICACY EQUAL OR BETTER THAN DOXORUBICIN IN A DOXORUBICIN-NAIVE PDX MODEL, 3) DEMONSTRATE ANTI-CANCER EFFICACY IN BOTH MALE AND FEMALE MICE, 4) ESTABLISH CONTRIBUTION OF MTM TO ANTI-CANCER EFFICACY FROM THAT OF RS-5. IN PHASE II, WE WILL PERFORM PRE-INVESTIGATIONAL NEW DRUG (IND) AND IND-ENABLING STUDIES WITH POTENTIAL EXPANSION INTO OTHER STS SUBTYPES THROUGH ADDITIONAL EFFICACY STUDIES. THE MEASURE OF SUCCESS FOR PHASE II IS 1) DEMONSTRATE COMPARABLE OR BETTER ANTI-CANCER EFFICACY OF RS-5 AT A WELL-TOLERATED DOSE TO THAT OF DOXORUBICIN AT A WELL-TOLERATED DOSE IN AT LEAST 1 ADDITIONAL PDX MODEL, 2) THE SUCCESSFUL VALIDATION OF BIO- ANALYTICAL METHODS FOR NONCLINICAL TOXICOLOGY SPECIES AND HUMANS, AND 3) CONDUCT IND-ENABLING STUDIES. COMPLETION OF THIS FAST-TRACK PROPOSAL WILL RESULT IN VALIDATION OF STS AS OUR FIRST CLINICAL INDICATION FOR RS-5 AND COMPLETION OF THE IND-ENABLING STUDIES TO SUPPORT THE CLINICAL DEVELOPMENT OF RS-5. ONCE COMPLETED, THE PHASE I AND II WORK WILL PROVIDE A RAPID PATH FOR RS-5 TO OBTAIN APPROVAL FOR PHASE I CLINICAL TESTING. | $2.1M | FY2023 | Aug 2023 – Jul 2026 |
| Department of Energy | MULTI-STROKE VARIABLE DISPLACEMENT OSCILLATING PUMP FOR HYDROKINETIC ENERGY | $1.3M | FY2019 | Jul 2019 – Aug 2022 |
| Department of Energy | WAVE-POWERED DESALINATION SYSTEM | $1.1M | FY2017 | Jun 2017 – Jan 2021 |
| Department of Energy | MARINE AND HYDROKINETIC TECHNOLOGY DEVELOPMENT AND ADVANCEMENT | $1.1M | FY2018 | Sep 2018 – Aug 2022 |
| Department of Energy | OPTIMAL CONTROL OF A SURGE-MODE WEC IN RANDOM WAVES | $808.7K | FY2014 | Feb 2014 – Apr 2016 |
| Department of Energy | WAVE-ACTUATED POWER TAKE OFF DEVICE FOR ELECTRICITY GENERATION | $320K | FY2011 | Dec 2010 – Oct 2012 |
| Department of Energy | NEW SBIR PHASE I 2009: ER85416 TITLE: ADVANCED WATER POWER TECHNOLOGY DEVELOPMENT WAVE AND CURRENT ENERGY TECHNOLOGIES. | $199.9K | FY2009 | Sep 2009 – Apr 2010 |
| Department of Energy | NEREUS™ – POWERING AUVS USING OCEAN WAVES | $198.9K | FY2020 | Jun 2020 – Jun 2021 |
| Department of Agriculture | DLT GRANTS- CARES ACT - MEDICAL | $0 | FY2021 | Jan 2021 – Jan 2023 |
Department of Energy
$2.1M
TAS::89 0227::TAS RECOVERY; NEW PHASE I SBIR: RECOVERY ACT; TITLE: RECOVERY ACT - A VARIABLE-GEOMETRY OSCILLATING WAVE SURGE CONVERTER PADDLE FOR MAX
Department of Health and Human Services
$2.1M
TARGETING MACROPHAGES TO TREAT SOFT TISSUE SARCOMAS - PROJECT SUMMARY SOFT TISSUES SARCOMAS (STS) IS A BROAD TERM FOR MULTIPLE SUBTYPES OF CANCER THAT START IN SOFT TISSUES. MOST STS ARE TREATED IN THE SAME WAY IN THE CLINIC REGARDLESS OF THE SUBTYPE. STS ENCOMPASSES OVER 50 HISTOLOGIC AND MOLECULAR SUBTYPES, WITH EACH DISPLAYING VARIABLE CLINICAL BEHAVIOR. THERE IS CURRENTLY NO UNIFYING TREATMENT FOR STS SUBTYPES BEYOND SURGERY, CHEMOTHERAPY, AND RADIATION. RESOLUTE SCIENCE INC. IS DEVELOPING NOVEL STS THERAPY BY USING TAMS TO PROCESS AND DELIVER ANTI-CANCER AGENTS TO SOLID TUMORS. TARGETING TAMS TO KILL THE ASSOCIATED CANCER HAS THE ADVANTAGE OF BEING TUMOR-AGNOSTIC COMPARED TO THAT OF TARGETING A SPECIFIC CANCER CELL RECEPTOR. THIS APPROACH BYPASSES CONCERNS OF TUMOR HETEROGENEITY AND EVOLVED RESISTANCE ASSOCIATED WITH THERAPEUTICS THAT TARGET SPECIFIC PROPERTIES OF EACH CANCER TYPE. OUR LEAD THERAPEUTIC, RS-5, IS WELL-TOLERATED AND DEMONSTRATED STRONG ANTI-CANCER EFFICACY ACROSS MULTIPLE MURINE SARCOMA TUMOR MODELS, INCLUDING THE SUBCUTANEOUS (SC) AND INTRACRANIAL (IC) HT1080 SARCOMA CELL LINE MODEL AND A DOXORUBICIN-RESISTANT PATIENT DERIVED XENOGRAFT (PDX) SARCOMA MODEL. RESOLUTE’S MODULAR DRUG DESIGN ALLOWS FOR STRAIGHTFORWARD CHEMICAL SUBSTITUTIONS OF LIGAND, BACKBONE, LINKER, AND PAYLOADS. FINALLY, THE COST OF COMMERCIAL MANUFACTURING WILL BE SIGNIFICANTLY LOWER THAN THAT OF ANTIBODIES AND ANTIBODY-DRUG CONJUGATES (ADCS) WHICH COULD SIGNIFICANTLY REDUCE THE PRICE OF THIS CANCER TREATMENT FOR PATIENTS AND INSURERS. THE OVERALL GOAL OF THE FAST-TRACK PROGRAM IS TO CONDUCT STUDIES THAT FURTHER SHOW THE EFFICACY OF RESOLUTE’S PLATFORM MOLECULE AS THERAPY FOR DIFFERENT STS SUBTYPES AND PERFORM PRE-INVESTIGATIONAL NEW DRUG (IND) AND IND-ENABLING STUDIES. OUR PHASE I GOAL FOR THIS SBIR FAST-TRACK PROPOSAL IS TO VALIDATE THE CHOICE OF ONE SUBTYPE OF STS, UNDIFFERENTIATED PLEOMORPHIC SARCOMA (UPS) AS AN INITIAL CLINICAL INDICATION FOR RS-5. THE MEASURE OF SUCCESS TO ADVANCE TO PHASE II IS 1) ESTABLISH DOSE RESPONSE OF RS-5 IN A DOXORUBICIN-RESISTANT UPS MODEL, 2) ESTABLISH ANTI-CANCER EFFICACY EQUAL OR BETTER THAN DOXORUBICIN IN A DOXORUBICIN-NAIVE PDX MODEL, 3) DEMONSTRATE ANTI-CANCER EFFICACY IN BOTH MALE AND FEMALE MICE, 4) ESTABLISH CONTRIBUTION OF MTM TO ANTI-CANCER EFFICACY FROM THAT OF RS-5. IN PHASE II, WE WILL PERFORM PRE-INVESTIGATIONAL NEW DRUG (IND) AND IND-ENABLING STUDIES WITH POTENTIAL EXPANSION INTO OTHER STS SUBTYPES THROUGH ADDITIONAL EFFICACY STUDIES. THE MEASURE OF SUCCESS FOR PHASE II IS 1) DEMONSTRATE COMPARABLE OR BETTER ANTI-CANCER EFFICACY OF RS-5 AT A WELL-TOLERATED DOSE TO THAT OF DOXORUBICIN AT A WELL-TOLERATED DOSE IN AT LEAST 1 ADDITIONAL PDX MODEL, 2) THE SUCCESSFUL VALIDATION OF BIO- ANALYTICAL METHODS FOR NONCLINICAL TOXICOLOGY SPECIES AND HUMANS, AND 3) CONDUCT IND-ENABLING STUDIES. COMPLETION OF THIS FAST-TRACK PROPOSAL WILL RESULT IN VALIDATION OF STS AS OUR FIRST CLINICAL INDICATION FOR RS-5 AND COMPLETION OF THE IND-ENABLING STUDIES TO SUPPORT THE CLINICAL DEVELOPMENT OF RS-5. ONCE COMPLETED, THE PHASE I AND II WORK WILL PROVIDE A RAPID PATH FOR RS-5 TO OBTAIN APPROVAL FOR PHASE I CLINICAL TESTING.
Department of Energy
$1.3M
MULTI-STROKE VARIABLE DISPLACEMENT OSCILLATING PUMP FOR HYDROKINETIC ENERGY
Department of Energy
$1.1M
WAVE-POWERED DESALINATION SYSTEM
Department of Energy
$1.1M
MARINE AND HYDROKINETIC TECHNOLOGY DEVELOPMENT AND ADVANCEMENT
Department of Energy
$808.7K
OPTIMAL CONTROL OF A SURGE-MODE WEC IN RANDOM WAVES
Department of Energy
$320K
WAVE-ACTUATED POWER TAKE OFF DEVICE FOR ELECTRICITY GENERATION
Department of Energy
$199.9K
NEW SBIR PHASE I 2009: ER85416 TITLE: ADVANCED WATER POWER TECHNOLOGY DEVELOPMENT WAVE AND CURRENT ENERGY TECHNOLOGIES.
Department of Energy
$198.9K
NEREUS™ – POWERING AUVS USING OCEAN WAVES
Department of Agriculture
$0
DLT GRANTS- CARES ACT - MEDICAL
Source: Federal Audit Clearinghouse (fac.gov)
No federal single audit records found for this organization.
Single audits are required for entities expending $750,000+ in federal awards annually.
Tax Year 2024 · Source: IRS e-Filed Form 990
Individuals serving as officers, directors, or trustees of the organization.
| Name | Title | Hrs/Wk | Compensation | Related Orgs | Other |
|---|
Source: IRS Publication 78, Auto-Revocation List & e-Postcard Data
Tax-deductible contributions: Yes
Deductibility code: PC
Sources: IRS e-Filed Form 990 (XML) & ProPublica Nonprofit Explorer
Scroll →
| Year | Revenue | Contributions | Expenses | Assets | Net Assets |
|---|---|---|---|---|---|
| 2024IRS e-File | $333.9K | $168.3K | $360.3K | $288K | $283.6K |
| 2023 | $406.4K | $196K | $340.7K | $313.3K | $310K |
| 2022 | $376.4K | $160.1K | $305.5K | $251.1K | $244.4K |
| 2021 | $290K | $131.9K |
Sources: ProPublica Nonprofit Explorer & IRS e-File Index
| Tax Year | Form Type | Source | Documents |
|---|---|---|---|
| 2024 | 990 | IRS e-File | PDF not yet published by IRSView Filing → |
| 2023 | 990 | DataIRS e-File | PDF not yet published by IRSView Filing → |
| 2022 | 990 | DataIRS e-File |
Financial data: IRS e-Filed Form 990 (Tax Year 2024)
Leadership & compensation: IRS e-Filed Form 990, Part VII (Tax Year 2024)
Federal grants: USAspending.gov (live)
Organization info: IRS Business Master File
Tax-deductibility: IRS Publication 78
| Total |
|---|
| Vince Miller | President | 40 | $106K | $0 | $65K | $171K |
Vince Miller
President
$171K
Hrs/Wk
40
Compensation
$106K
Related Orgs
$0
Other
$65K
Members of the governing board. Board members often serve without compensation.
| Name | Title | Hrs/Wk | Compensation | Related Orgs | Other | Total |
|---|---|---|---|---|---|---|
| Mike Nowezki | Board Chair | 1 | $0 | $0 | $0 | $0 |
| Pat Watson | Treasurer | 1 | $0 | $0 | $0 | $0 |
| Steve Braatz | Secretary | 1 | $0 | $0 | $0 | $0 |
Mike Nowezki
Board Chair
$0
Hrs/Wk
1
Compensation
$0
Related Orgs
$0
Other
$0
Pat Watson
Treasurer
$0
Hrs/Wk
1
Compensation
$0
Related Orgs
$0
Other
$0
Steve Braatz
Secretary
$0
Hrs/Wk
1
Compensation
$0
Related Orgs
$0
Other
$0
| $264.4K |
| $179.5K |
| $173.4K |
| 2020 | $276.3K | $86.8K | $257.5K | $149.9K | $147.9K |
| 2019 | $254.3K | $105.8K | $243.5K | $140.4K | $129.1K |
| 2018 | $257.7K | $133.5K | $219.8K | $124.4K | $118.3K |
| 2017 | $249K | $174.8K | $318.9K | $98K | $80.4K |
| 2016 | $390.1K | $301.3K | $380.2K | $169.7K | $150.3K |
| 2015 | $382K | $337.5K | $370.9K | $142.4K | $140.4K |
| 2014 | $214.7K | $185.5K | $85K | $131K | $129.3K |
| 2021 | 990 | Data | PDF not yet published by IRS |
| 2020 | 990 | Data |
| 2019 | 990 | Data |
| 2018 | 990 | Data |
| 2017 | 990 | Data |
| 2016 | 990 | Data |
| 2015 | 990 | Data |
| 2014 | 990 | Data |