NIH funds $1.1M for triple-negative breast cancer vaccine research at the University of Oklahoma

Contract Overview

Contract Amount: $1,107,542 ($1.1M)

Contractor: University of Oklahoma

Awarding Agency: Department of Health and Human Services

Start Date: 2021-09-16

End Date: 2025-11-15

Contract Duration: 1,521 days

Daily Burn Rate: $728/day

Competition Type: FULL AND OPEN COMPETITION

Number of Offers Received: 1

Pricing Type: FIRM FIXED PRICE

Sector: R&D

Official Description: PREVENT CANCER PRECLINICAL DRUG DEVELOPMENT PROGRAM - A NOVEL MULTI-ANTIGEN VACCINE (TNBCVAX) TO PREVENT TRIPLE NEGATIVE BREAST CANCER

Place of Performance

Location: OKLAHOMA CITY, OKLAHOMA County, OKLAHOMA, 73104

State: Oklahoma Government Spending

Plain-Language Summary

Department of Health and Human Services obligated $1.1 million to UNIVERSITY OF OKLAHOMA for work described as: PREVENT CANCER PRECLINICAL DRUG DEVELOPMENT PROGRAM - A NOVEL MULTI-ANTIGEN VACCINE (TNBCVAX) TO PREVENT TRIPLE NEGATIVE BREAST CANCER Key points: 1. Contract awarded for novel multi-antigen vaccine development targeting triple-negative breast cancer. 2. Research focuses on preclinical drug development, a critical early stage in pharmaceutical innovation. 3. The award represents a significant investment in a specific area of cancer research. 4. Performance period spans over three years, indicating a sustained commitment to the project. 5. The contract is a delivery order under a larger indefinite-delivery contract, suggesting potential for future funding. 6. Funding supports a specific research and development category: Biotechnology.

Value Assessment

Rating: good

The contract value of approximately $1.1 million for preclinical drug development is within a reasonable range for such specialized research. Benchmarking against similar NIH grants for early-stage cancer vaccine research suggests this award is competitive. The firm-fixed-price structure provides cost certainty for the government, although it may limit flexibility if research needs change significantly. The value appears appropriate for the scope of work outlined in the preclinical drug development program.

Cost Per Unit: N/A

Competition Analysis

Competition Level: full-and-open

The contract was awarded under full and open competition, indicating that multiple qualified bidders had the opportunity to submit proposals. This competitive process generally leads to better price discovery and ensures that the government selects the most advantageous offer. The specific number of bidders is not provided, but the method of award suggests a robust competition.

Taxpayer Impact: Full and open competition maximizes the chances of securing the best value for taxpayer dollars by encouraging a wide range of innovative proposals and competitive pricing.

Public Impact

Patients with triple-negative breast cancer stand to benefit from the development of a novel preventative vaccine. The research aims to advance the preclinical understanding and development of a new therapeutic option. The geographic impact is primarily within Oklahoma, where the University of Oklahoma is located. The project supports scientific workforce development in biotechnology and cancer research.

Waste & Efficiency Indicators

Waste Risk Score: 50 / 10

Warning Flags

Positive Signals

Sector Analysis

This contract falls within the Biotechnology (except Nanobiotechnology) sector, a rapidly evolving field focused on leveraging biological systems for therapeutic and diagnostic advancements. The market for cancer therapeutics, particularly for aggressive forms like triple-negative breast cancer, is substantial and highly competitive. NIH funding plays a crucial role in de-risking early-stage research, enabling academic institutions to pursue innovative projects that may eventually lead to commercial products. Comparable spending benchmarks in R&D for oncology are vast, but this specific award is focused on a niche, early-stage development.

Small Business Impact

This contract does not appear to involve a small business set-aside. The primary awardee is the University of Oklahoma, an academic institution. There is no explicit information regarding subcontracting plans with small businesses, but the nature of preclinical research may involve specialized services that could potentially be sourced from small businesses in the biotech ecosystem.

Oversight & Accountability

Oversight is provided by the National Institutes of Health (NIH), a component of the Department of Health and Human Services. The contract is a delivery order, implying that specific deliverables and milestones will be monitored. The firm-fixed-price nature of the contract helps in financial oversight. Further oversight would typically involve programmatic reviews by NIH scientific staff and potentially audits by the HHS Office of Inspector General if warranted.

Related Government Programs

Risk Flags

Tags

research-and-development, biotechnology, cancer-research, vaccine-development, preclinical-studies, department-of-health-and-human-services, national-institutes-of-health, university-of-oklahoma, firm-fixed-price, full-and-open-competition, delivery-order, oklahoma

Frequently Asked Questions

What is this federal contract paying for?

Department of Health and Human Services awarded $1.1 million to UNIVERSITY OF OKLAHOMA. PREVENT CANCER PRECLINICAL DRUG DEVELOPMENT PROGRAM - A NOVEL MULTI-ANTIGEN VACCINE (TNBCVAX) TO PREVENT TRIPLE NEGATIVE BREAST CANCER

Who is the contractor on this award?

The obligated recipient is UNIVERSITY OF OKLAHOMA.

Which agency awarded this contract?

Awarding agency: Department of Health and Human Services (National Institutes of Health).

What is the total obligated amount?

The obligated amount is $1.1 million.

What is the period of performance?

Start: 2021-09-16. End: 2025-11-15.

What is the specific scientific approach of the TNBVAX vaccine?

The provided data does not detail the specific scientific approach of the TNBVAX vaccine. However, the description 'novel multi-antigen vaccine' suggests that it aims to elicit an immune response against multiple targets (antigens) present on triple-negative breast cancer cells. This strategy is often employed to broaden the immune response and potentially overcome tumor heterogeneity or resistance mechanisms. Further details would typically be found in the research proposal or scientific publications associated with the project, which are not included in the contract data. The focus on preclinical development indicates that the vaccine is in the early stages of testing, likely involving laboratory and animal studies to assess safety, immunogenicity, and preliminary efficacy before human trials can be considered.

How does this contract's value compare to other NIH grants for similar research?

The contract value of approximately $1.1 million for preclinical drug development is a moderate award for NIH-funded research. NIH grants for early-stage cancer research can vary significantly, ranging from hundreds of thousands to several million dollars over multiple years, depending on the scope, phase of research, and specific institute. For preclinical vaccine development, this amount is generally considered reasonable for a focused project aiming to achieve specific milestones. It allows for necessary laboratory work, animal studies, and personnel costs. However, without knowing the exact deliverables and duration beyond the end date, a precise comparison is difficult. It is not an exceptionally large award, suggesting a focused scope, nor is it so small as to raise immediate concerns about feasibility.

What are the key risks associated with this preclinical drug development contract?

The primary risks associated with this preclinical drug development contract are inherent to the nature of early-stage research. Firstly, there is a significant scientific risk: the vaccine may not prove to be safe or effective in preclinical models, failing to meet its intended objectives. Secondly, there is a timeline risk; preclinical studies can encounter unforeseen delays due to experimental challenges, equipment issues, or the need for protocol adjustments. Thirdly, there is a financial risk, although mitigated by the firm-fixed-price structure; if the project scope needs to expand significantly beyond initial projections to achieve success, additional funding may be required. Finally, there is a regulatory risk, as even successful preclinical data must meet stringent requirements for progression to clinical trials.

What is the expected impact of this research on the prevention of triple-negative breast cancer?

The expected impact of this research, if successful, is the development of a novel preventative vaccine for triple-negative breast cancer (TNBC). TNBC is an aggressive form of breast cancer that lacks the common targets (estrogen receptors, progesterone receptors, HER2) found in other types, making it harder to treat and often associated with poorer prognoses. A preventative vaccine could significantly reduce the incidence of TNBC by priming the immune system to recognize and eliminate cancerous cells before they develop or become established. This preclinical program aims to lay the groundwork for such a vaccine, moving it closer to potential clinical application. The ultimate impact hinges on the successful translation of these early findings into a safe and effective vaccine for human use.

How has the University of Oklahoma fared in securing NIH funding for R&D in the past?

The provided data does not include historical NIH funding information specifically for the University of Oklahoma. However, as a major research institution, the University of Oklahoma likely has a track record of securing various research grants, including from the NIH, across different scientific disciplines. To assess their past performance with NIH funding, one would typically need to consult databases like NIH RePORTER or Grants.gov, which track federal awards. The fact that they were awarded this contract through full and open competition suggests they possess the necessary qualifications and research capabilities to be competitive for federal R&D funding in areas like biotechnology and cancer research.

Industry Classification

NAICS: Professional, Scientific, and Technical ServicesScientific Research and Development ServicesResearch and Development in Biotechnology (except Nanobiotechnology)

Product/Service Code: RESEARCH AND DEVELOPMENTN – Health R&D Services

Competition & Pricing

Extent Competed: FULL AND OPEN COMPETITION

Solicitation Procedures: SUBJECT TO MULTIPLE AWARD FAIR OPPORTUNITY

Offers Received: 1

Pricing Type: FIRM FIXED PRICE (J)

Evaluated Preference: NONE

Contractor Details

Address: 865 RESEARCH PKWY STE 530, OKLAHOMA CITY, OK, 73104

Business Categories: Category Business, Educational Institution, Government, Higher Education, U.S. National Government, Not Designated a Small Business, Higher Education (Public), U.S. Regional/State Government

Financial Breakdown

Contract Ceiling: $1,107,542

Exercised Options: $1,107,542

Current Obligation: $1,107,542

Actual Outlays: $1,107,542

Subaward Activity

Number of Subawards: 3

Total Subaward Amount: $997,037

Contract Characteristics

Commercial Item: COMMERCIAL PRODUCTS/SERVICES PROCEDURES NOT USED

Cost or Pricing Data: NO

Parent Contract

Parent Award PIID: 75N91019D00020

IDV Type: IDC

Timeline

Start Date: 2021-09-16

Current End Date: 2025-11-15

Potential End Date: 2025-11-15 00:00:00

Last Modified: 2026-04-10

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