SBIR/STTR Research Award

Graft-protective properties of LGM2605 in Lung Transplantation

Award identifier 03bb8877072d706594dd61742013a2da68478835e29858b17a4617a5a7f931deAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$299,599

Program and phase

STTR · Phase I

Award year

2018

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Lignamed, LLC
Proposal award date
2018-08-01
Contract end date
2019-07-31
UEI
C8L8WEU3TE85
Solicitation number
PA17-303
Topic code
NHLBI

Research abstract

LignaMedLLC is developing LGMa novel medical device that will be administered via an FDA approved ex vivo lung perfusion deviceEVLPto improve lung function parameters of ex vivo donor lungs in advance of transplant surgeryPer FDA device regulations LGMwill be fully flushed and cleared from the donor lung prior to transplantThe major challenge with lung transplantation is the oxidative damage that occurs during lung storageThis reduces the availability of lungs for transplant andprimesthe donor lung to recruit polymorphonuclear neutrophilsPMNfrom the transplant recipientRecruited PMN adhere to the vessel wall of the newly transplanted lunggrafttransmigrate and release myeloperoxidaseMPOan enzyme stored in neutrophils and macrophages responsible for hypochlorous acid generation causing injury to the graftRecognizing the role of PMN in injury and eventual poor transplant outcomethe clinical strategy at present is to block PMN activation by a non specific immunosuppression regimen administered to the transplant recipientHoweverimmunosuppression therapy has severe side effectsLignaMed proposes the use of LGMa synthetic small molecule agent to adampen inflammatory pathways in the donor lung and binhibit MPO activation in recruited PMNPreliminary data show that LGMprotects human donor lungs but the mechanism of protection has not been elucidatedIn the proposed Phase I study we will determine the immunomodulatory properties of LGMto modulate the pro inflammatory phenotype of stored human and mouse donor lungscold storageAimand reduce PMN adherence and activation during warm reperfusion by monitoringexogenousPMN adherenceMPO inhibition and subsequent lung injuryAimIf data obtained from the proposed human and mouse donor lungs show a significant reduction in PMN recruitmentadherence and subsequent tissue injurywe will be enabled to proceed to Phase II with a full clinical and analytical evaluation of this agent for an eventual FDA approvalOur focus onpre treatmentof a donor organprior to transplantwith LGMconstitutes a paradigm shift from the current transplant related therapies LignaMedLLCis developing LGMas a device for use in lung transplantIn this application we propose to treat donor lungsrather than the current clinical practice of treating theliverecipientwith LGMa device which blocks a cascade of damaging signals on the donor lung that predispose it to beinginjuredafter transplantElucidation of the mechanism by which this protection occurs is the focus of this work

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

7 SBIR/STTR records share this UEI (2017–2020). Reported award amounts total $7,077,331. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services, National Aeronautics and Space Administration

Agency intelligence

Department of Health and Human Services

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