SBIR/STTR Research Award

Development of new anti-inflammatory peptides for treatment of type I diabetes

Award identifier 38bfbd22d41376c318a58c94205aed9a35c7c6d41256bc920651ddc1392608f5Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$142,970

Program and phase

SBIR · Phase I

Award year

2013

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
SERPIN PHARMA, LLC
Proposal award date
Not reported
Contract end date
Not reported
UEI
YPS8G6GE19J4
Solicitation number
PA12-088
Topic code
NIDDK

Research abstract

DESCRIPTION (provided by applicant): Type I diabetes is an autoimmune disease where auto-immunity leads to slow, progressive destruction of pancreatic -cells and development of overt diabetes. Currently, there is no cure for type I diabetes, which is treated with insulin replacement therapy by daily injections. Immune modulation has the potential to arrest -cell destruction and several therapeutic strategies have shown great promise, although none have been identified which permanently prevents -cell destruction in new onset diabetic patients. Recent studies in the mouse non-obese diabetic (NOD) model of type I diabetes show that specific regulatory immune cell populations (Tregs) can arrest -cell destruction, and that agents which induce these Tregs can prevent type I diabetes in NOD animals. This proposal will test if a new therapeutic peptide, SP16, can be used to induce expansion of protective Treg populations in the NOD mouse model and thereby provide protection against beta-cell destruction and development of type I diabetes. Specifically, the experiments will test the hypothesis that SP16 treatment reverses new onset diabetes in NOD mice by stimulating expansion of tolerogenic APC and Treg populations. SP16 treatment is predicted to eliminate insulitis and restore normoglycemia in the NOD animals. If the data from the proposed study show that SP16 protects against development of type I diabetes, this will justify a formal preclinical development program, as well as a follow-on Phase II SBIR application, with the goal of submitting an Investigation New Drug (IND) application to the FDA in 2013. A successful IND submission would pave the way for a Phase I Clinical Trial, in new-onset pediatric type I diabetes patients or adult LADA patients (latent autoimmune diabetes in adults), where efficacy would result in improved C-peptide levels and suggest a potential paradigm shift in treatment of type I diabetes. PUBLIC HEALTH RELEVANCE PUBLIC HEALTH RELEVANCE: The aim of this project is to test anew, therapeutic peptide drug for treatment and reversal of new-onset type I diabetes. There are currently no treatments, which can prevent or cure type I diabetes and patients are confined to insulin replacement therapy by daily insulin injections. Poorcompliance is associated with risk of serious complications. This new peptide drug has tremendous potential for improving patient quality of life and reducing health care associated costs.

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

4 SBIR/STTR records share this UEI (2013–2024). Reported award amounts total $2,194,361. 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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