Opportunity Information: Apply for DARPA BAA 11 30
Apply for DARPA BAA 11 30
- The DARPA Microsystems Technology Office in the science and technology and other research and development sector is offering a public funding opportunity titled "Dialysis Like Therapeutics (DLT)" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 12.910 Research and Technology Development.
- This funding opportunity was created on Feb 8, 2011 and posted on Feb 8, 2011.
- Applicants must submit their applications by Apr 1, 2011 Important Dates Posting Date February 8, 2011 Proposers Day Date February 23, 2011 in Arlington, VA Full Proposal Due Date April 1, 2011. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
- Eligible applicants include: Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled Additional Information on Eligibility.
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Opportunity Summary:
The Dialysis Like Therapeutics (DLT) opportunity (DARPA BAA 11-30) is a Defense Advanced Research Projects Agency program run through DARPA's Microsystems Technology Office (MTO) that sought research proposals aimed at a major battlefield and critical care problem: sepsis, a life-threatening systemic blood infection and inflammatory syndrome that can rapidly lead to organ failure and death. The central idea behind DLT is to move beyond conventional drug-only approaches by creating a portable, device-based therapy that can actively manage and rebalance the bloodstream itself. DARPA framed the desired end capability as a compact system that can control relevant components across the entire blood volume on clinically meaningful time scales, implying rapid, whole-blood intervention rather than slow, partial, or highly localized treatment.
Technically, the program emphasized that achieving this kind of blood-management capability would require breakthroughs across several tightly connected areas. First, advanced sensing would be needed to detect and track the blood markers and physiological signals that matter during sepsis, potentially including pathogens, toxins, inflammatory mediators, immune factors, and other circulating components that change quickly as a patient deteriorates or responds to treatment. Second, the device concept depends on sophisticated fluid handling, meaning the ability to move, meter, and route complex biological fluids reliably, likely under challenging operational conditions. Third, DARPA highlighted separation and selective removal or modulation of components within blood, which implies approaches analogous to (but more capable than) dialysis or hemofiltration: extracting harmful elements, preserving beneficial ones, and potentially adding or adjusting therapeutic factors without destabilizing the patient. Finally, the program called for mathematical descriptions and control strategies capable of predictive, closed-loop operation, where real-time measurements feed into models and algorithms that decide how the device should adjust its actions, with the goal of maintaining or restoring stability in a rapidly evolving disease state.
In practical terms, the DLT program was aiming at a field-deployable, clinically useful platform that could be used to treat sepsis and its complications, with the stated expectation that such a device could save the lives of thousands of military patients each year. The emphasis on portability suggests use cases beyond large hospital intensive care units, including forward operating environments or transport scenarios where time-to-treatment and logistical constraints are severe. The overall vision combines diagnostics, therapeutic blood processing, and automated control into a single integrated system, effectively turning sepsis management into an engineered, feedback-controlled process rather than a largely reactive clinical effort.
From an administrative standpoint, this was a discretionary federal funding opportunity under the DARPA Broad Agency Announcement mechanism (Funding Opportunity Number: DARPA BAA 11-30; Title: Dialysis Like Therapeutics). It supported science and technology and other research and development activities (CFDA 12.910, Research and Technology Development) and allowed multiple funding instruments including cooperative agreements, grants, other procurement contracts, and similar arrangements. The listing did not specify an award floor or ceiling (both shown as 0 in the source data), which typically indicates that funding levels would be determined based on the quality, scope, and negotiated structure of proposed research efforts rather than a fixed, pre-published range. Cost sharing or matching was not required. Eligibility was listed as unrestricted, meaning that any type of entity could apply subject to any additional eligibility clarifications in the full announcement.
Key dates included a posting date of February 8, 2011, a Proposers Day held February 23, 2011 in Arlington, Virginia (a common DARPA practice to brief potential proposers and encourage teaming), and a full proposal due date of April 1, 2011. The opportunity later moved into archive status with an archive date of October 3, 2011. The announcement directed applicants to the MTO solicitations page for additional information and provided a contact for access issues: Dr. Timothy Broderick, DARPA Program Manager and BAA Coordinator.
Dialysis Like Therapeutics (DLT) (DARPA BAA 11-30) - FAQs
1) What is the Dialysis Like Therapeutics (DLT) opportunity?
Dialysis Like Therapeutics (DLT) is a DARPA funding opportunity released under Broad Agency Announcement DARPA BAA 11-30. It sought research proposals to develop a portable, device-based therapeutic approach for managing sepsis by actively monitoring and rebalancing the bloodstream, rather than relying only on conventional drug treatments.
2) Which government agency and office ran this program?
The program was run by the Defense Advanced Research Projects Agency (DARPA) through DARPA's Microsystems Technology Office (MTO).
3) What problem was DLT trying to solve?
DLT targeted sepsis, described as a life-threatening systemic blood infection and inflammatory syndrome that can rapidly lead to organ failure and death. DARPA framed it as a major battlefield and critical care problem.
4) What was the core technical vision behind DLT?
The central idea was to move beyond drug-only approaches by creating a compact, portable system that can actively manage the bloodstream itself. DARPA described the desired end capability as controlling relevant components across the entire blood volume on clinically meaningful time scales, implying rapid, whole-blood intervention.
5) What kinds of capabilities was the proposed device expected to have?
Based on the description, the envisioned platform combines diagnostics, therapeutic blood processing, and automated control into one integrated system. It would measure relevant blood and physiological signals, process blood to remove or modulate harmful components while preserving beneficial ones, and adjust operation using predictive, closed-loop control.
6) What did DARPA mean by "clinically meaningful time scales" and "entire blood volume"?
In this context, DARPA signaled interest in rapid, whole-blood intervention rather than slow, partial, or highly localized treatment. The idea was to affect the blood system broadly and quickly enough to matter during fast-changing sepsis progression.
7) What technical areas did DARPA emphasize as necessary breakthroughs?
DLT emphasized several tightly connected areas: (1) advanced sensing, (2) sophisticated fluid handling, (3) separation and selective removal or modulation of blood components, and (4) mathematical descriptions and control strategies for predictive, closed-loop operation.
8) What types of sensing were relevant to DLT?
DARPA highlighted advanced sensing to detect and track markers and physiological signals relevant to sepsis, potentially including pathogens, toxins, inflammatory mediators, immune factors, and other circulating components that can change rapidly as the patient deteriorates or responds to treatment.
9) What did the program mean by "fluid handling"?
Fluid handling referred to the ability to move, meter, and route complex biological fluids (blood) reliably, potentially under challenging operational conditions. This suggests robust, controlled handling of blood and related fluids as part of an integrated device.
10) What did DARPA mean by "separation and selective removal or modulation" of blood components?
The description implies approaches analogous to, but more capable than, dialysis or hemofiltration: extracting harmful elements, preserving beneficial ones, and potentially adding or adjusting therapeutic factors without destabilizing the patient.
11) Was this program specifically about dialysis machines?
The program used dialysis as an analogy ("dialysis-like") but emphasized more advanced capabilities than conventional dialysis or hemofiltration, including selective removal/modulation of components and integration with sensing and closed-loop control.
12) What is meant by "predictive, closed-loop operation" in DLT?
Predictive, closed-loop operation refers to using real-time measurements as inputs to mathematical models and control algorithms that decide how the device should adjust its actions. The goal is to maintain or restore stability in a rapidly evolving disease state.
13) What was the intended operational setting for the DLT technology?
DARPA emphasized a field-deployable, portable, clinically useful platform. The portability focus suggests use beyond large hospital intensive care units, including forward operating environments or transport scenarios with severe time-to-treatment and logistical constraints.
14) Who was expected to benefit from the technology if successful?
The opportunity stated an expectation that such a device could save the lives of thousands of military patients each year, indicating strong relevance to military medicine and battlefield/operational care.
15) What type of funding opportunity was DLT?
DLT was a discretionary federal funding opportunity issued under the DARPA Broad Agency Announcement (BAA) mechanism (Funding Opportunity Number: DARPA BAA 11-30; Title: Dialysis Like Therapeutics).
16) What research category or assistance listing applied to this opportunity?
The listing identified CFDA 12.910, Research and Technology Development, and described the supported activities as science and technology and other research and development.
17) What funding instruments were allowed under this opportunity?
The opportunity allowed multiple funding instruments, including cooperative agreements, grants, other procurement contracts, and similar arrangements.
18) Were minimum or maximum award amounts specified?
No. The source data showed an award floor of 0 and an award ceiling of 0, which typically indicates funding levels would be determined based on the quality and scope of proposed efforts and negotiations, rather than a fixed published range.
19) Was cost sharing or matching required?
No. Cost sharing or matching was not required.
20) Who was eligible to apply?
Eligibility was listed as unrestricted, meaning any type of entity could apply, subject to any additional eligibility clarifications in the full announcement.
21) What were the key dates for this opportunity?
The posting date was February 8, 2011. A Proposers Day was held February 23, 2011 in Arlington, Virginia. The full proposal due date was April 1, 2011. The opportunity later moved to archive status, with an archive date of October 3, 2011.
22) What was the Proposers Day and where was it held?
The Proposers Day was a DARPA event to brief potential proposers and encourage teaming. For DLT, it was held February 23, 2011 in Arlington, Virginia.
23) Where were applicants directed to look for additional information?
The announcement directed applicants to the Microsystems Technology Office (MTO) solicitations page for additional information.
24) Who was the contact person for access issues related to the announcement?
The provided contact for access issues was Dr. Timothy Broderick, DARPA Program Manager and BAA Coordinator.
25) Is this opportunity still open?
No. The opportunity moved into archive status, with an archive date of October 3, 2011.
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