SBIR/STTR Research Award

Effectiveness of VBP15, a dissociative steroidal analogue, on inflammation in a mouse model of arthritis

Award identifier 76763783ff9911d918d2eab25fda129c4f10ea980f41a9c662429c66075a5cd1Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$225,000

Program and phase

STTR · Phase I

Award year

2015

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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
2015-09-01
Contract end date
2016-08-31
UEI
NQA4J3L3E1Z4
Solicitation number
PA14-072
Topic code
NIAMS

Research abstract

DESCRIPTION provided by applicant Glucocorticoids GCandapos s such as prednisolone are used frequently to induce remission and treat rheumatoid arthritis RA Despite effectiveness many GC mediated detrimental side effects including osteoporosis and muscle atrophy limit long term chronic treatment of RA patients In addition juvenile arthritis patients suffer from th side effect of significant stunting of linear growth These side effects are believed to be mediated by well described glucocorticoid response element GRE mediated transcriptional properties transactivation whereas efficacy is mediated by transrepression of NFkB pro inflammatory pathways ReveraGen BioPharma has identified a lead compound VBP that is a novel dissociative steroid designed to maintain the anti inflammatory efficacy of traditional steroids through NFkB inhibition and GR translocation yet has lost GRE mediated transcriptional activities leading to much less side effects typically associated with traditional glucocorticoid drugs no osteopenia growth stunting or steroid myopathy Importantly VBP has been shown to reduce inflammatory activity in vivo across multiple murine models of disease Furthermore we have demonstrated in a pilot study that VBP significantly reduces the severity of disease in the collagen antibody induced mouse model of arthritis preliminary data Thus VBP may represent a safer and more effective alternative to traditional glucocorticoids in the treatment of RA where treatment of elderly RA patients may show efficacy with loss of osteopenia and steroid myopathy side effects and loss of growth stunting side effects important in juvenile RA The goal of this STTR research is to extend preclinical evaluation of VBP with a blinded study of efficacy endpoints in a chronic collagen induced mouse model of arthritis CIA using published recommendations for pre clinical studies We hypothesize that VBP treatment after disease onset will result in similar anti inflammatory activity compared to prednisolone but possess a much reduced side effect profile As VBP has already entered Phase clinical trials in adult healthy volunteers transition to RA trials would likely ensure shortly after the successful completion of the proposed STTR grant PUBLIC HEALTH RELEVANCE The goal of this STTR research is to extend preclinical evaluation of VBP with a blinded study of efficacy endpoints in a chronic collagen induced mouse model of arthritis using published recommendations for pre clinical studies VBP may represent a safer and more effective alternative to traditional glucocorticoids in the treatment of rheumatoid arthritis

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.

Agency intelligence

Department of Health and Human Services

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