Portable electronically controlled transdermal patch for enfuvirtide delivery

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$1,957,909.00
Award Year:
2012
Program:
SBIR
Phase:
Phase II
Contract:
2R44AI080335-02A1
Award Id:
n/a
Agency Tracking Number:
R44AI080335
Solicitation Year:
2012
Solicitation Topic Code:
NIAID
Solicitation Number:
PA11-096
Small Business Information
310 ROLLING RIDGE DR, BELLEFONTE, PA, -
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
Y
Duns:
791379030
Principal Investigator:
MAUREENMULVIHILL
(814) 355-0003
mmulvihill@actuatedmedical.com
Business Contact:
MAUREENMULVIHILL
(814) 355-0003
mmulvihill@actuatedmedical.com
Research Institute:
n/a
Abstract
DESCRIPTION (provided by applicant): In this Phase II NIH SBIR, Piezo Resonance Innovations will further optimize and test the Portable Transdermal Patch (PTP) - a needle-free platform delivery technology for drugs and vaccines that are currently deliveredsubcutaneously. The portable, 200gm (7oz) electronically-controlled transdermal patch for Enfuvirtide delivery employs a patented transducer technology with integrated battery driven controls to deliver drugs as prescribed. The low power of the PTP transducers will open 25 to 125 5m micro-channels in the stratum corneum, without causing long-term skin damage. Thirty-three million people worldwide are living with the Human Immunodeficiency Virus (HIV). Currently, patients infected with HIV receive Highly Active Antiretroviral Therapy (HAART) for the management of the infection. Medication regimens for the management of HIV must be taken with near-perfect compliance to maximize benefits and prevent development of viral resistance. Enfuvirtide, approved by theFood and Drug Administration in 2003, is an infusion inhibitor that blocks the HIV from attaching to the CD4 cell. It is subcutaneously injected twice daily and directed at patients not responding to other treatments. The major side effect is an injectionsite reaction, which reduces patient compliance substantially. A needle-free device that enhances patient compliance with Enfuvirtide, and other large-molecule medication regimes, like insulin, will be of great benefit. Phase I developed and tested prototypes and met all of the Specific Aims. Transdermal delivery of Enfuvirtide was demonstrated in pig skin models. Reviews by practicing clinicians were positive and have been used to guide the Phase II Beta prototype design requirements. Phase II will optimize the PTP performance characteristics and electronic control into a small lightweight, ergonomic patch. Safety and efficacy of the PTP will then be evaluated in a live animal model. The PTP Transdermal Delivery Technology will: Deliver Enfuvirtide (T-20) Transdermally, increasing patient regime compliance Eliminate the injection site reaction that limits T-20 adoption Act as a platform technology to deliver other large molecule medications (e.g. insulin) Be comfortable to wear, painless during operation, and hide discretely under clothing. Deliver medications through a prescription reservoir that holds dosing for multiple days. Deliver lower dose, sustained delivery - rather than large bolus dosage. PUBLIC HEALTH RELEVANCE: This Phase II NIH SBIR will finalize development of a Portable, Lightweight Electronically-Controlled Transdermal Patch platform device. The patch will be a needle-free, automatic and safe ultrasonic drug delivery device to keep HIV patients in medication regime compliance - with potential application in a wide range of other medications, such as insulin.

* information listed above is at the time of submission.

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