SBIR/STTR Research Award

Building an evidentiary case for circulating GHBP as a biomarker for drug-associated stunting of growth

Award identifier 96f328580f836196d8f04a96ab7fe0b70afeb1dcd02dcd2db5f2b6d91754d2ceAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$224,998

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
REVERAGEN BIOPHARMA, INC.
Proposal award date
2018-07-01
Contract end date
2020-06-30
UEI
NQA4J3L3E1Z4
Solicitation number
PA16-303
Topic code
NICHD

Research abstract

There is increasing interest in the use of biomarkers in clinical drug developmentwith much of thest Century Cures Act focused on encouraging this approachIdeallybiomarkers could provide and acute and objective read out of drug mechanism of actionpharmacodynamic biomarkersor prediction of later clinical benefit or harmsurrogate outcome measureHoweververy few biomarkers have been validated for routine use in drug developmentThis is due to the need to fulfill stringent yet reasonable requirements at multiple levelsincluding defining specific context of useshowing that a specific biomarker is fit for purposein a context of useand demonstrating assay validity for assessments of the biomarkerprecisionsensitivityreliabilityGlucocorticoidsprednisolone and deflazacortare among the most extensively prescribed drugswith aboutmillion prescriptions per year in the USThey show potent anti inflammatory efficacybut also extensive safety concerns with long term use in chronic inflammatory statesparticularly in pediatricsStunting of growth is seen with both prednisone and deflazacort treatmentand is one of the chief complaints of patients and families regarding side effects of these drugsWhile stunting of growth is a clear safety concern of importance to patients and familiesit is challenging to accurately assess in clinical trials due to the large variance in growth rates of different childrenHerewe propose research focused on building an evidentiary package on the use of circulating GHBPgrowth hormone binding proteinas a surrogate biomarker anticipating later stunting of growth as a safety concern of drug treatmentReveraGen Biopharma is a privately owned small business based in RockvilleMDIn published pre clinical studies in mouse models of human chronic inflammatory stateswe demonstrated that glucocorticoid induced growth stunting could be assessed after aweek prednisolone regimen and that this in vivo assay is sufficient to compare different treatments in terms of their ability to cause stunted growthFurthermorein our recently published pharmacodynamic biomarker studies of anti inflammatories in children we found the extracellular domain of human growth hormone receptorgrowth hormone binding proteinGHBPto be at high levels in the sera of glucocorticoid treated childrenIn unpublished data in the mdx model of DMDwe found prednisolone to result in increased GHBP in serumAs GHBP is considered inhibitory to hGH GHR signalingwe hypothesize that steroid induced GHBP may be a biomarker predictive of later growth stunting!Stunting of growth is seen with glucocorticoid treatmentand is one of the chief complaints of patients and families regarding side effects of these drugsHoweverit is challenging to accurately assess growth stunting in clinical trials due to the large variance in growth rates in different childrenThe goal of the proposed STTR research is to build an evidentiary case for GHBP as afit for purposebiomarker for monitoring of druginduced stunting of growth

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

11 SBIR/STTR records share this UEI (2010–2020). Reported award amounts total $11,189,078. Reported amounts are not federal obligations.

Phases: Phase I, Phase II, Phase II – Direct to Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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