Development of concentrated and rapidly absorbed insulins for closed loop systems

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$582,473.00
Award Year:
2012
Program:
SBIR
Phase:
Phase I
Contract:
1R43DK096604-01
Award Id:
n/a
Agency Tracking Number:
R43DK096604
Solicitation Year:
2012
Solicitation Topic Code:
NIDDK
Solicitation Number:
DK11-018
Small Business Information
100 SAW MILL RD, DANBURY, CT, -
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
145773359
Principal Investigator:
ROBERT HAUSER
(203) 796-5000
rhauser@biodel.com
Business Contact:
PATRICK SIMMS
(203) 796-5000
psimms@biodel.com
Research Institute:
Stub




Abstract
DESCRIPTION (provided by applicant): Extreme insulin resistance in patients with diabetes is defined as insulin dose requirement of greater than 200 units daily. Currently, U-500 regular insulin is frequently used to treat these patients, however, the slowabsorption and prolonged duration of action associated with this formulation does not lend itself to effective closed loop insulin pump therapy. A more rapidly absorbed formulation of concentrated insulin would be desirable in this scenario and would provide the additional benefit of taking up less volume than current insulin preparations. Biodel has studied formulations of recombinant human insulin designed for ultra-rapid absorption at meal time. These formulations use EDTA to chelate zinc atoms, destabilizing recombinant human insulin hexamers. Citric acid is also used to mask surface charges on the insulin molecules inhibiting re-aggregation of monomers and directly facilitating absorption. Experiments to date have shown that EDTA/citrate based formulations at concentrations of up to 400 units/ml remain soluble and stable at 5 C. In this application, Biodel proposes to optimize multiple pH 7 aqueous formulations of concentrated recombinant human insulin together with excipients which in U-100 formulations have been shown to be ultra-rapid acting, to provide a minimum of 18 month stability under refrigerated conditions. We will ensure that all current US Pharmacopeia (USP) compendia methods are applicable to these formulations and will develop suitable methods if required. We will demonstrate biological activity in a diabetic swine model and will demonstrate that our formulation is compatible with a marketed insulin pump system for at least 14 days. PUBLIC HEALTH RELEVANCE: Severe insulin resistance in patients with diabetes is defined as insulin dose requirement of greater than 200 units daily. This is usually treated with U-500 regular insulin, the use of which has nearly doubled since 2008. U-500 is associated with long period to peak effect anda prolonged duration of action, both of which make it not desirable for use in pumps, particularly in the setting of closed loop insulin systems. A more rapidly absorbed formulation of concentrated insulin would be desirable in this setting and would provide the additional benefit of taking up less space than current insulin preparations. In this application, Biodel proposes a strategy to develop concentrated insulin with more rapid absorption properties for use in insulin pumps.

* information listed above is at the time of submission.

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