SBIR/STTR Research Award

IMPROVED HYPOGLYCEMIA RESCUE DEVICE

Award identifier d468637fef5e7f5c22c42277617025343c0b9e62678282501f614852d800bb3bAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$157,478

Program and phase

SBIR · Phase I

Award year

2009

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Xeris Pharmaceuticals, Inc.
Proposal award date
Not reported
Contract end date
Not reported
UEI
YAV5AK7VKJ31
Solicitation number
PHS2009-2
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): The objective of this program is to develop of a clinical prototype, semi-solid drug formulation and auto-injector pen that deliver microliter volumes of a glucagon dose without reconstitution for hypoglycemic emergencies. To assess the feasibility of this objective, it is necessary to first demonstrate that glucagon can be formulated into an ultra- concentrated, semi-solid formulation and second, that glucagon in a semi-solid formulation is bioavailable and bioactive following subcutaneous delivery. If successful, these experiments will lead to development of a simple, portable, glucagon delivery system for use in a Phase 1/2 safety-pharmacokinetics study. The first Specific Aim of this proposed project is to develop a prototype formulation of human glucagon that meets defined criteria for functionality in the delivery device, dissolution in an in vitro model of interstitial fluid and demonstration of short-term, accelerated stability of the glucagon formulation. The second Specific Aim is the successful in vivo delivery of formulations in clinically relevant doses in a rat model. Formulations will be judged by 1) gt80% dissolution of glucagon in simulated interstitial fluid and 2) lt10% residual drug in the device after administration. In addition, one (1) months of chemical and physical stability (gt95% API content and equivalent viscosity to day 0) of the solid glucagon formulation will be deemed successful. Effective subcutaneous delivery of glucagon will be assessed by measurement of the drug in the blood using radioimmunoassay. Bioavailability of gt80% relative to a control subcutaneous injection of aqueous-reconstituted glucagon in a rat model will be deemed successful. Meeting these criteria will justify further development of this novel glucagon delivery system. PUBLIC HEALTH RELEVANCE: The current standard of care for hypoglycemic emergencies-- the glucagon Emergency Kit requires a diabetic's caregiver to reconstitute the peptide powder contained in a vial using a 1 mL prefilled syringe and to assure complete solubilization prior to injection. A patient friendly, ready-to-use auto-injector Glucagon Pen will reduce caregiver and patient fear and risk, costs of 911 calls and emergency room visits.

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.

Research funding history

12 SBIR/STTR records share this UEI (2009–2017). Reported award amounts total $9,300,227. Reported amounts are not federal obligations.

Phases: Phase II, Phase I

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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