DAXOR CORPORATION — Department of Defense SBIR Phase II: A18-122
DAXOR CORPORATION — SBIR Phase II award from Department of Defense.
Phase II SBIR prototype / development signal
- Phase II is where Department of Defense funds deeper R&D after feasibility. Incumbents with Phase II history are serious competitors on adjacent topics.
- Use this award as past-performance context and to map customer organizations for STRATFI/TACFI-style transition planning.
- Obligated amount $1,099,997 is consistent with substantial Phase II-scale effort; compare to related awards from the same agency.
- Topic code A18-122 links this award to a solicitation family — search the same topic stem for incumbents and recompete timing.
- Amount
- $1,099,997
- Agency
- Department of Defense · Defense Health Program
- Program / Phase
- SBIR · Phase II
- Topic
- A18-122
- Solicitation
- 18.2
- NAICS
- —
- Place of performance
- TN
- Period
- 2023-06-29 → 2025-11-02
Description
Hemorrhage is the leading cause of preventable combat mortality. Despite recent advances in care, sustaining adequate tissue perfusion remains a challenge. Current practice for determining fluid status to guide battlefield resuscitation and transfusion, including clinical assessment and surrogate markers, often lag symptomatic diagnosis or misdiagnose the severity of volume derangement. Care is further complicated by the risks of under- and over-resuscitation, high patient heterogeneity, and scarcity of resources, especially during prolonged field care, and multi-domain operations. Precise guidance of fluid resuscitation and blood transfusion therefor remain urgent unmet operational priorities. Blood volume analysis (BVA) [BVA-100; Daxor Corporation, Oak Ridge, TN] is the only FDA-cleared method utilizing the gold standard indicator dilution technique for quantifying intravascular Blood Volume (BV). Extensive peer-reviewed medical literature has validated BVA’s enhancement of interventions through rapid, reliable, and accurate BV quantification. Daxor Corporation has successfully completed Phase I and II U.S. Army SBIR contracts to develop a rapid, portable, and robust point-of-care (POC) BVA system. The new diagnostic capability is designed to meet combat casualty care and civilian hospital clinical specifications, including demonstrated diagnostic accuracy and functionality for combat casualty and standard civilian clinical use. A prototype of the new device has been validated against the existing GS system to meet contract milestones, including to have greater than 95% accuracy quantifying patient BV, to provide patient-specific fluid resuscitation and red blood cell transfusion guidance. To complete requirements for the POC BVA system, the proposed sequential Phase II SBIR contract will support the completion of the following objectives: 1. Complete Design and Validation of POC instrument; 2. Obtain 510(k) clearance; 2. Pilot Build and Initial Rollout; and, 4. EMR integration. As a company publicly listed on the NASDAQ stock exchange with full time business, technical, and sales and marketing teams, Daxor is well positioned to complete the proposed technology development effort and successfully commercialize the resultant product.