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Fiscal Receipts

Biomedical Technology

DARPARDT&EReconciledPE0602115E
What it is
Biomedical Technology (0602115E) is a DARPA research & development line funded in the Research, Development, Test and Evaluation, Defense-Wide account. Its J-book detail breaks the line into 1 project.
What changed
No FY25→26 comparison — endpoints unavailable or on different bases.
Who gets it
No single contractor is published as this line's leader. 13 linked award records are listed below. This line's high-confidence links do not clear the floor for a published concentration index — at least 3 awards across 2 contractor families holding positive obligations, with positive net linked dollars. Why the crosswalk is partial.

Budget figures

FY24 Actuals
$106.6MR-1 TOA · PB2026
FY25 Total
$132.6MR-1 TOA · PB2026
FY26 Request
$0J-book detail · PB2026
FY25→26 Change
No comparison: endpoints unavailable or on different bases

No FY2026 R-1/P-1 request line for this program element. The FY2026 President's Budget request workbook carries no FY2026 line for it; its last workbook figure is FY2025. The PB2026 J-book detail below does carry an FY2026 row for this line, recorded as zero. A workbook blank and a documented zero are different records, and this page shows both. An absent line is not by itself an ending — PB2026 renumbered program elements at scale across the services and defense agencies, so this work may continue under a different number. No successor is linked for this line: this site's program-lineage layer holds no keyed edge pointing forward from here. That is an absence in this site's lineage layer, not a finding about the program: if the J-book narrative on this page describes a realignment, it is quoted below in the document's own words, and this note does not restate it.

Data coverage

FY2026 award data is a partial year — USAspending reports awards on a rolling basis, and this corpus runs through 2026-09-04. why partial FY2026 data? →

Budget trajectory

The program's 3 summary figures for FY24 to FY26, plotted in fiscal-year order: this line ends lower than it starts. The points are the summary cards above, not a separate derivation; the table beside the chart carries each figure with its own citation.
The program's 3 summary figures for FY24 to FY26, plotted in fiscal-year order: this line ends lower than it starts. The points are the summary cards above, not a separate derivation; the table beside the chart carries each figure with its own citation.FY24: $106.6MFY25: $132.6MFY26: $0FY24FY25FY26
Budget trajectory: one row per fiscal year, carrying the summary figure the sparkline plots. Every figure opens its own citation.
Fiscal yearAmount
FY24$106.6MR-1 TOA · PB2026
FY25$132.6MR-1 TOA · PB2026
FY26$0J-book detail · PB2026

Decade view

P-1/R-1 workbook TOA basis, shown compact in $B/$M (the workbook records USD thousands); each figure cites its own President's Budget edition

11 fiscal years of this program as published (FY2015–FY2025): a line through the actuals (filled dots), with the enacted (hollow circles) and request (diamonds) markers each edition reported. Read it for direction, not for precision — this program's actuals line falls across the span. The grid below is the same data as text, one cited figure per cell.
11 fiscal years of this program as published (FY2015–FY2025): a line through the actuals (filled dots), with the enacted (hollow circles) and request (diamonds) markers each edition reported. Read it for direction, not for precision — this program's actuals line falls across the span. The grid below is the same data as text, one cited figure per cell.FY2015 actuals — PB2017 editionFY2016 actuals — PB2018 editionFY2017 actuals — PB2019 editionFY2018 actuals — PB2020 editionFY2019 actuals — PB2021 editionFY2020 actuals — PB2022 editionFY2021 actuals — PB2023 editionFY2022 actuals — PB2024 editionFY2023 actuals — PB2025 editionFY2024 actuals — PB2026 editionFY2016 enacted — PB2017 editionFY2017 enacted — PB2018 editionFY2018 enacted — PB2019 editionFY2019 enacted — PB2020 editionFY2020 enacted — PB2021 editionFY2021 enacted — PB2022 editionFY2022 enacted — PB2023 editionFY2023 enacted — PB2024 editionFY2024 enacted — PB2025 editionFY2025 enacted — PB2026 editionFY2017 request — PB2017 editionFY2018 request — PB2018 editionFY2019 request — PB2019 editionFY2020 request — PB2020 editionFY2021 request — PB2021 editionFY2022 request — PB2022 editionFY2023 request — PB2023 editionFY2024 request — PB2024 editionFY2025 request — PB2025 editionFY15FY17FY19FY21FY23FY25

The vertical scale does not start at zero: the baseline sits just below this program’s smallest year, so a low point on this line is not a small amount. Read the shape for direction and the grid below for the figures.

● actuals (line)  ·  ○ enacted  ·  ◇ request — gaps are editions the program is absent from, never interpolated.

Decade series values by fiscal year and President's Budget edition: one row per series (actuals, enacted, request), one column per fiscal year. Every figure opens its own citation.
SeriesFY15FY16FY17FY18FY19FY20FY21FY22FY23FY24FY25
Actuals$164.6M$120.5M$95.8M$89.0M$94.4M$131.0M$98.3M$100.5M$104.2M$106.6M
Enacted$114.3M$115.2M$109.4M$101.3M$92.8M$107.6M$108.7M$127.0M$141.1M$132.6M
Request$115.2M$109.4M$101.3M$97.8M$107.6M$108.7M$107.0M$141.1M$169.2M

blank = series not published for this year; – = absent from that edition.

Asked vs spent: the PB2024 book requested $141.1M for FY2024; the PB2026 book reported $106.6M as actual total obligation authority — $34.5M below the request. 106.6 − 141.1 = -34.5 USD millions — the compact figures above are rounded for reading.

Program lineage

No predecessor/successor lineage was recorded for this program element — no FY-to-FY transfer into or out of this line was stated in the ingested J-books, and none was inferred from the program structure.

Description

Mission — BIOMEDICAL TECHNOLOGY

The Biomedical Technology Program Element (PE) focuses on applied research for medical related technologies that will maintain warfighter health and performance before, during, or after operations. Successful technologies within this Program Element will maintain warfighter health against emerging threats through novel biothreat detection, rapid medical countermeasure identification and development, and distributed production of effective therapeutics. In-theater, warfighter health will be maintained through the development of field-relevant technologies such as reliable and accessible critical medical resources, novel detection and protection capabilities for traumatic brain injury, and rapid, effective triage of battlefield injuries. Technologies are also being developed to provide new capabilities for warfighter recovery from sustained injury including, but not limited, to spinal cord injury. Additionally, this PE will improve warfighter readiness by characterizing and assaying physical and cognitive performance to drive data-driven awareness. This PE also supports innovation and robust transition planning in the technology cycle by working with entrepreneurs to increase the likelihood that DARPA-funded technologies take root in the U.S. and provide new capabilities for national defense. Beginning in FY 2026, efforts in this PE will be funded in PE 0602024E, Warfighting Performance.

Justification

Accomplishments & Planned Programs (15)

Rapid Battlefield Triage

The Rapid Battlefield Triage program is advancing capabilities to quickly triage warfighters requiring urgent life-saving medical intervention and enable medical resources to provide an appropriate response in current and future battlefields. Today, triage at point-of-injury is limited by subjective assessments, tools that are manually intensive, and physiological signatures with little diagnostic and prognostic value. This program will build on recent biomarker discoveries and innovations in sensing platforms to develop field-portable technologies that support triage in the most challenging operational domains. By optimizing allocation of scarce medical resources and scaling to multiple casualties, these devices will help far-forward units maximize their fighting strength against adversaries that inflict large numbers of casualties and constrain evacuation to advanced medical facilities. Beginning in FY 2026, this program will be funded in PE 0602024E, Project WP-02.

Neurological Assessment and Protection from Brain Injury

The Neurological Assessment and Protection from Brain Injury program is transforming our current detection and protection strategies against traumatic brain injury (TBI), such as injury from blast exposure. This program is developing prophylactic countermeasures to prevent severe brain injury. Current available tools in far forward operating domains for these injuries are lacking especially those that effectively discriminate between mild- and medium-level trauma. These novel technologies will change the paradigm for treatment of TBI by preventing injury rather than attempting to reverse or repair it. Beginning in FY 2026, this program will be funded in PE 0602024E, Project WP-02.

Reengineering Enabling Sleep Transition in Operationally Restrictive Environments (RESTORE)

The Reengineering Enabling Sleep Transition in Operationally Restrictive Environments (RESTORE) program aims to enhance the efficiency of sleep to optimize warfighter performance following sleep restriction, as commonly occurs in combat operations. Sleep is a critical factor in cognitive function and decision-making, yet the tempo of military operations often results in acute and chronic sleep restriction. To optimize sleep recovery in such conditions, RESTORE seeks to develop a multi-modal system that enables precision control of sleep macro- (i.e., orchestration of transition between sleep phases) and micro-architectures (i.e., efficiency within sleep phases). By optimizing efficiency of recovery despite sleep restriction, RESTORE seeks to enable warfighter to perform at their best, even in the most challenging operational environments, and to enhance their overall readiness and effectiveness. Beginning in FY 2026, this program will be funded in PE 0602024E, Project WP-02.

Bridging the Gap after Spinal Cord Injury

The Bridging the Gap after Spinal Cord Injury program is developing and integrating technologies to heal and restore function associated with spinal cord injuries. This program will significantly advance treatment technologies by developing implantable, adaptive devices to address different stages of spinal cord injury. For early phases of injury, this program will develop technologies for real-time biomarker tracking and delivery of therapies to stabilize or rebuild nerve connections at the injury site. For final phase of injury, the Bridging the Gap after Spinal Cord Injury program will develop and integrate a network of devices deployed across the body to effectively create a synthetic nervous system and "bridge the gap" of the spinal cord injury to restore function and sensory feedback. The Bridging the Gap after Spinal Cord Injury program will dramatically improve the quality of life for wounded warfighters and veterans suffering from spinal cord injuries.

Deployable Medical Countermeasures for Warfighter Readiness

Maintaining robust protection and treatment against infectious disease threats during stabilization operations (e.g., Humanitarian and Disaster Relief [HADR]) requires rapid drug discovery and reducing manufacturing and supply chain burdens. A major limitation of our current response to emerging biological and chemical threats is the lack of immediate availability of ideal medical countermeasures (MCMs) for rapid response, which includes high quality nucleic acid templates for MCM manufacturing. These nucleic acids are also critical for research and development (R&D) applications ranging from synthetic biology to the testing and development of medical countermeasures. Current U.S.-based DNA production capabilities are limited to less than a handful of manufacturers; it takes weeks to months to produce adequate quality and quantity of DNA at these manufacturing sites and ship them to downstream partners. The Deployable Medical Countermeasures for Warfighter Readiness program is developing an on-demand deployable platform to manufacture nucleic acid drugs safely at scale, in short timeframes. The platform will be comprised of a fully contained system capable of selectively manufacturing relevant doses of current Good Manufacturing Process (cGMP) grade nucleic acid therapeutics at or near the point of care. This effort will also develop high quality gene-length DNA for R&D. This on-demand platform will enable countermeasures capable of combating novel threats, allowing a small force to prevent regional outbreaks from becoming global emergencies.

Distributed Access to Critical Biotherapeutics for Warfighters

The goal of the Distributed Access to Critical Biotherapeutics for Warfighters program was to ensure DoD access to critical medical countermeasures (MCMs) by establishing the foundational technologies needed for fully distributable, on-demand manufacturing of protein-based MCMs and critical reagents. To achieve this, investments were made in technologies that enabled immediate, high-yield synthesis of bioactive protein MCMs. This effort reduced the risk associated with the development of cell-free protein synthesis systems that support access to DoD-relevant therapeutic proteins and bolstered the biomanufacturing industrial base.

Forensic Indicators of Threat Exposure (FITE)

The DoD responds to a variety of chemical, biological, and radiological threats around the globe that require protective medical countermeasures that ensure force health protection and warfighter readiness. The Forensic Indicators of Threat Exposure (FITE) program has developed a field-deployable resource that revealed an individual's exposure history to chemical, biological, and radiological threats by characterizing epigenetic signatures in an individual's genome and other biological responses. The program has created the framework for modular technology capable of performing forensic or diagnostic analysis using epigenetic information that provided high specificity of the type of exposure and when it occurred. This novel capability served as a field-forward forensic tool for use by the DoD and assisted in Chemical, Biological, Radiological, and Nuclear (CBRN) threat detection and response.

GOLDen hour extended EVACuation (GOLDEVAC)

Survival from combat trauma is predicated on a rapid sequence of events that escalate care as soon as possible. The GOLDen hour extended EVACuation (GOLDEVAC) program is developing new technologies that will provide medical care closer to the point of injury and facilitate effective evacuation. This will extend the time available to evacuate injured service members to higher levels of care. Building upon technologies discovered under the Rapid Battlefield Triage program (budgeted in PE 0602115E, Project BT-01), this program will explore technologies that enable autonomous care of patients and/or which act as force multipliers that enable caregivers to effectively take care of larger number of patients. Beginning in FY 2026, this program will be funded in PE 0602024E, Project WP-02.

Next-Generation Combat Casualty Care

The Next-Generation Combat Casualty Care program is developing advances in critical efforts to preserve warfighter life and well-being in the battlefields of the future. This research will directly address a leading cause of potentially preventable battlefield casualties by investigating new approaches for developing whole blood substitutes for traumatic injury that can be deployed on the battlefield in far forward settings. Additional potential uses apply to disaster relief, mass casualty events, and stabilization missions. Advances within this program will ensure that the U.S. remains able to care for service members in peer and near-peer conflict by addressing gaps in combat casualty care. Beginning in FY 2026, this program will be funded in PE 0602024E, Project WP-02.

Improved Personnel Placement (IPP)

The Improved Personnel Placement (IPP) program aims to improve force lethality and overmatch by developing assays to determine physical/cognitive states in order to maximize performance and resilience, while minimizing attrition. IPP will identify and measure biomarkers for unique physical, cognitive, and behavioral traits associated with a broad spectrum of military specialties. This knowledge will help individualize training and provide novel measures of physical/cognitive states for specialized roles, while providing training cadres greater precision for predicting candidate readiness without bias. Measuring an individual's biological system will ensure that they achieve their maximum potential while facilitating readiness and resilience for the DoD. Beginning in FY 2026, this program will be funded in PE 0602024E, Project WP-02.

Novel Delivery Technology for Medical Countermeasures

The DoD requires rapid development of medical countermeasures (MCM) to ensure force health protection and improve our ability to respond to emerging and novel biological threats. Despite recent advancements in development of new MCMs, challenges with delivery limits their current therapeutic potential. While emerging targeted delivery systems such as polymer/lipid nanoparticles and viral vectors have enabled the delivery of large, complex MCM molecules, they are still plagued by lack of widespread availability and effectiveness. Investing in efficient, adaptable delivery technology is crucial for strengthening biosecurity preparedness and will enable rapid response to the evolving biological threat landscape, whether the threat is natural or manmade. The Novel Delivery Technology for Medical Countermeasures program will develop minimally invasive MCM delivery systems, in which any therapeutic can be quickly formulated and administered to treat or prevent any disease. Developing novel delivery platforms will maintain warfighter health and readiness and enable rapid response to existing and novel biothreats. Beginning in FY 2026, this program will be funded in PE 0602024E, Project WP-02.

Red Blood Cell Factory (RBC-Factory)

Warfighters operate in extreme, austere, and dangerous domains that stress physiology, contain pathogens, and compromise health and performance. Protective equipment often hinders performance (e.g., loss of dexterity, rapid overheating, visual obstruction, etc.) and pharmacological approaches can carry unpleasant-to-dangerous side effects. The Red Blood Cell Factory (RBC-Factory) program will explore the limits of what biologically active components, or cargoes, can be placed inside red blood cells (RBCs) to help protect the warfighter from within. Cargoes can include natural or synthetic products and may not perturb the physiological characteristics that allow RBCs to safely operate in a body. RBC-Factory aims to deliver a method capable of high-throughput modification of RBCs and a knowledge product identifying what kinds of cargo and how many can be put inside an RBC. RBC-Factory will determine if RBCs are a suitable vector for medium-term passive protection for warfighters against threats and, if so, de-risk future programs that operationalize the technology for specific applications. Beginning in FY 2026, this program will be funded in PE 0602024E, Project WP-02.

Alert WARfighter Enablement (AWARE)

The Alert WARfighter Enablement (AWARE) program is developing a combination drug and device to non-invasively increase alertness following sleep loss in humans, without negative side effects, and with reduced addictive potential. AWARE program goals include developing candidate photoswitchable molecules that can be reversibly activated in the presence of near infrared (NIR) light, and wearable device elements that emit NIR light to activate the candidate molecules. The combination of an ingested photoswitchable molecule and a NIR-emitting device will selectively activate neural pathways responsible for executive function, working memory, and decision making, wherever and whenever both drug and light are simultaneously present. If successful, AWARE technology will enable warfighters to maintain cognitive function and alertness during long-range missions and to obtain restorative sleep when needed, without negative side effects. Beginning in FY 2026, this program will be funded in PE 0602024E, Project WP-02.

Controlled Genome Protection

The Controlled Genome Protection program will develop advanced capabilities to control and tune the activity of gene editing technologies. Advances in synthetic biology have significantly expanded the suite of genome editors and modulators available. Many of the new genome editors have been identified from rare, slow-growing microorganisms with unique metabolic capabilities. New tools across these new classes of genome editors are required to advance our understanding of, our control of, and ultimately our leverage of gene editing technologies across all domains of life. Advances within this program will ensure that the U.S. leads innovation in this widespread, advancing field that poses potential national security threats due to the large-scale democratization of gene editing technologies. Beginning in FY 2026, this program will be funded in PE 0602024E, Project WP-02.

BioElectronics to Sense and Treat (BEST)

The BioElectronics to Sense and Treat (BEST) program seeks to improve warfighter recovery from battlefield injuries by developing technologies to diagnose, prevent, and treat wound infections in real-time. This program will generate high-resolution sensors that continually monitor a wound by assessing the community composition of contaminating microorganisms and/or the host immune response. Data from these sensors will be used to predict if a wound will become infected and to regulate the targeted administration of known and novel treatments to prevent infections or resolve existing infections. Ultimately, the sensor and treatment elements will be combined into a closed-loop smart bandage that can provide rapid diagnostics and precise treatments at all levels of deployed military medical care. Beginning in FY 2026, this program will be funded in PE 0602024E, Project WP-02.

Budget line items(workbook-cited)

P-1/R-1 workbook Total Obligation Authority basis (USD thousands) · PB2026.

Exhibit R-1

AccountOrgTypeAmount
Research, Development, Test and Evaluation, Defense-WideDARPAFY24 Actuals$106.6M
Research, Development, Test and Evaluation, Defense-WideDARPAFY25 Enacted$132.6M
Research, Development, Test and Evaluation, Defense-WideDARPAFY25 Total$132.6M

Budget Details(R-2/P-40 facts)

J-book detail basis (R-2/P-40, USD millions) · PB2026 — a different accounting basis from the P-1/R-1 workbook TOA above; where the two disagree, the reconciliation strip under Budget figures shows both.

Wider than this screen — swipe the table sideways for the remaining fiscal-year columns.

ProjectAll Prior YearsFY24 ActualsFY25 TotalFY26 BaseFY26 Request
Program Element$0$106.6M$132.6M$0$0
BT-01: BIOMEDICAL TECHNOLOGY$0$106.6M$132.6M$0$0

Follow the dollar

No follow-the-dollar view — this program's awards haven't been crosswalked at high confidence (flows cover 312 of 1,938 programs). why coverage is partial? →

Related awards

Award linkage is shown for 32 of 200 profiled companies — high- and medium-confidence USAspending matches, each row labeled; medium is the weaker evidence. why partial award coverage? →

Rows marked medium rest on evidence weaker than a program-level match, and of more than one kind. An account-based row, where the award drew from the same appropriation account as this program, is an association, not evidence that this program paid for the contract. Where the evidence is instead an FPDS acquisition-program tag or a subaward description, the program is established but which of its budget lines paid is not. An announcement link a recorded review did not leave standing is medium too. Only high rows rest on the contract naming this program with a recorded review upholding it and no recorded rejection or refutation applying.

RecipientPIIDConfidence
BAE SYSTEMS INFORMATION & ELECTRONIC SYSTEMS INTEGRATION INCHR001119C0017medium
BAE SYSTEMS INFORMATION AND ELECTRONIC SYSTEMS INTEGRATION INC.HR001113C0075medium
BAE SYSTEMS INFORMATION AND ELECTRONIC SYSTEMS INTEGRATION INC.HR001119C0054medium
BAE SYSTEMS INFORMATION AND ELECTRONIC SYSTEMS INTEGRATION INC.HR001119C0090medium
DATA MACHINES CORP.HR001118C0021medium
NORTHROP GRUMMAN SYSTEMS CORPORATIONHR001113C0077medium
NORTHROP GRUMMAN SYSTEMS CORPORATIONHR001119C0087medium
PHYSICAL SCIENCES INC.HR001118C0140medium
RTX BBN TECHNOLOGIES, INC.HR001116C0058medium
RTX CORPORATIONHR001115C0035medium
TELEDYNE SCIENTIFIC & IMAGING, LLCHR001116C0105medium
UNIVERSITY OF SOUTHERN CALIFORNIAHR001119C0048medium
UNIVERSITY OF SOUTHERN CALIFORNIAHR001119C0053medium

Contractor concentration

No concentration index is published for this line. This line's high-confidence links do not clear the floor for a published concentration index — at least 3 awards across 2 contractor families holding positive obligations, with positive net linked dollars. An index below that floor is a fact about the sample, not about the market. Whatever further links this line carries are medium-confidence, and what each medium evidence path does and does not establish is set out in the methodology. Both bases are in the downloadable warehouse.

Lobbying mentions

No Senate LDA lobbying filing in the tracked data mentions this program element by code or alias.

Oversight

Department-level designation (not specific to this program)

GAO lists 5 high-risk areas for DOD as a whole. That designation covers the department, not Biomedical Technology. No program-specific GAO finding for this line is in the ingested data. See the DOD oversight record.

Program dossier

No research dossier for this program — dossiers cover 50 of 1,938 programs, the largest fully J-book-detailed lines by FY2026 requested dollars. why no dossier here? →

Primary sources

Open any budget figure for its exact receipt. Verified line items lead with the highlighted government PDF; original spreadsheets download with their budget edition and exhibit in the filename.

Budget totals · TOA sources

Detailed budget justification

The related TOA spreadsheets above use a different accounting basis from R-2/P-40 detail. Their amounts are not assumed to match these detailed sources.