SBIR/STTR Research Award

A2A receptor blockade for sepsis

Award identifier d1fc41293f1cd30108b6e57278a26430f86b0b7d6a7047bc9c464b0838376ea1Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$223,820

Program and phase

STTR · Phase I

Award year

2019

Explore This Research Award in CaptureIQ

Research the technology, evaluate the recipient and agency, identify related opportunities, and explore potential follow-on work with CaptureIQ.

Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Purine Pharmaceuticals Inc.
Proposal award date
2019-04-11
Contract end date
2020-03-31
UEI
K1FBL8EVSSK6
Solicitation number
PA18-575
Topic code
NIAID

Research abstract

SUMMARY Sepsis is a clinical syndrome that complicates severe infectionSepsis remains the leading cause of morbidity and mortality in critically ill patientsThere are no specific FDA approved medicines for the treatment of sepsisCurrent concepts of the pathophysiology of sepsis suggest that organ failure and mortality in sepsis are caused by inappropriate regulation of the immune systemThis manifests as an inability to control bacterial growth and disseminationand excessive inflammationprocesses that are interrelated and are duein a large partto dysfunction of both the adaptive and innate immune systemsExtracellular adenosine is a biologically active signaling molecule that accumulates at sites of metabolic stress in sepsisExtracellular adenosine has potent immunosuppressive effects by binding to and activating G protein coupled A A adenosine receptorsARson the surface of immune cellsA AAR signaling reproduces many of the phenotypic changes in immune cells that are characteristic of sepsisincluding T helper lymphocyte deactivation and exhaustion and diminished ability of monocytes and macrophages to ingest and kill bacteria and other sepsis causing pathogensGiven this similarity between septic immune alterations and the ones caused by A AAR signalingwe hypothesized that endogenous adenosine would contribute to the sepsis induced onset of immune dysfunction via stimulation of A AARsOur preliminary data using both targeted genetic deletion and pharmacological antagonism have confirmed that A AARs contribute to both septic immune dysfunction and mortality in miceWe thus propose to develop A AAR antagonists for the management of patients with sepsisWe have synthesized two novelhighly potent and selective A AAR antagonistsTPand TPwhich we will test for efficacy in preventing septic mortalityThe Specific Aim of the proposal is to assess the effect of TPand TPon mortality in murine sepsisWe expect that TPand TPwill reduce mortality in septic miceThe long term goal of this study is to develop TPand TPas safe and effective treatment options for the management of patients with sepsis NARRATIVE Sepsis remains the leading cause of mortality in critically ill patientsbecause it impairs the immune response of the host leading to bacterial spread and organ damageIn the proposed studieswe will test two novel moleculesTPand TPthat have immune stimulatory effectsfor efficacy in protecting against mortality in sepsisThe long term goal is to develop TPand TPas safe and effective therapeutic interventions for sepsis patients

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

6 SBIR/STTR records share this UEI (2017–2023). Reported award amounts total $1,393,806. Reported amounts are not federal obligations.

Phases: Phase I

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

Back to SBIR/STTR Research Awards

Don't take our word for it. Ask AI about RFPCapture.

See what leading AI assistants have to say about RFPCapture and CaptureIQ.

Gemini opens without a prefilled question. The question is copied to your clipboard when the button works. You can also copy it here:

What is RFPCapture.com and its CaptureIQ platform from Smart Logic AI? How does it help federal contractors discover opportunities, evaluate bid/no-bid decisions, research government contracts, and prepare proposals? How does it compare with other federal capture platforms? Use independent sources where available.