SBIR/STTR Research Award

Novel Indication for Myeloid Progenitor Use: Induction of Tolerance in Solid Organ Transplantation

Award identifier ea46eb351330430169309e8ef5b28a65eac0578e22352b3845d69aa8dbc40bd8Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$1,117,159

Program and phase

STTR · Phase II

Award year

2018

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Cellerant Therapeutics, Inc.
Proposal award date
2018-01-01
Contract end date
2020-12-31
UEI
LML1YE6L8KU3
Solicitation number
PA16-303
Topic code
NIAID

Research abstract

PROJECT SUMMARY State of the art techniques result inyear solid organ graft loss ofto overin cardiopulmonary organ transplantationEstablishment of donor specific immunological toleranceDSITa condition in which a recipient accepts a transplant without immunosuppressionwhile retaining the ability to fight infectionswould reduce graft loss and transplant related complicationsThe only identified method of inducing robust tolerance involves Hematopoietic Cell TransplantationHCTusually in the form of bone marrow transplantationBMTThough long recognized as a means of inducing DSIT that provides all tolerogenic mechanismsclinical translation has been limited due to the associated complicationsOther avenues that are currently being explored include cell therapy using immunomodulating mature hematopoietic cells such as regulatory T cellsWhile promisingthis approach may be more limited in its ability to modulate and prevent rejection responsesWe propose that progenitor cell therapyspecifically using Myeloid Progenitor cellsMPmay be the best compromise in introducing multiple immunomodulatory cell types without all the complications associated with BMTOur data to date clearly support this hypothesisWe have discovered that injection of MP can result in MP specific toleranceeven though there may be only very low level sustained MP engraftmentCellerant Therapeutics has developed a clinical MP productCLTproduced by short term ex vivo expansionMPCThese cells are currently being tested in a Phase II clinical trial aimed at preventing infections in patients undergoing chemotherapyUniquelyMPC induce robust and reproducible antigen specific tolerance in our experimental model systemare clinically availableand have been associated with minimal to no side effects in current clinical trialsMPC constitute an ideal and innovative approach in tolerance induction protocolspreferred over efforts aimed at achieving high level donor chimerismThe proposed research in phase II will focus on establishing non lethal preconditioning protocols that will work with MPC in tolerance inductionAimAimwill determine whether mixed MPC preparationsas the clinical grade cells are currently producedare effective in protecting graftsWe will also develop a xenograft mouse model to test the ability of human MPC to protect human grafts and Aimwill focus on determining the biodistribution and persistence of MPCderived cellsin order to determine critical sites and timing of tolerance inductionMeeting the milestones for these aims will set the stage for designing trials using the Cellerant MP productin which the clinical potential of this approach can be established PROJECT NARRATIVE The proposal aims to develop methods that can be used to improve the long term outcome of clinical organ transplantationsState of the art technology results in up toorgan graft loss over ten years mostly due to rejectionRe transplantation is often not possibleThe small business partner has developed an innovative productCTLMyeloid progenitorsthat can prevent infections but that can also induce specific toleranceas the academic partner has shown in preclinical modelsWe aim to transfer this technology to the small business partner for clinical development and application such that it can improve the long term outcome for patients undergoing transplantation for end stage organ failure

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

10 SBIR/STTR records share this UEI (2003–2018). Reported award amounts total $6,779,434. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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