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The Retroject Device: A Novel Approach to Glaucoma Drug Delivery

Award Information
Agency: Department of Health and Human Services
Branch: National Institutes of Health
Contract: 1R41EY023860-01
Agency Tracking Number: R41EY023860
Amount: $159,063.00
Phase: Phase I
Program: STTR
Solicitation Topic Code: NEI
Solicitation Number: PA12-089
Solicitation Year: 2013
Award Year: 2013
Award Start Date (Proposal Award Date): N/A
Award End Date (Contract End Date): N/A
Small Business Information
United States
DUNS: 78672324
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 (919) 619-3042
Business Contact
Phone: (919) 619-3042
Research Institution
DUKE UNIVERSITY 2200 W Main St., Suite 820
DURHAM, NC 27705-
United States

 () -
 Nonprofit College or University

PROJECT ABSTRACT Glaucoma is a common neurodegenerative disease which is the 2nd leading cause of blindness in the United States. With the aging baby boomer population, these numbers will continue to increase exponentially over the next few decades. With glaucomatous progression, there is ultimately damage to the optic nerve which results in peripheral vision loss. It has been shown in many prior studies that lowering the intraocular pressure (IOP) is the best way to minimize the risk of progression of thedisease. The majority of glaucoma patients are treated with topical drops. However, there are many inherent issues that prevent adequate therapy including corneal transport inadequacy, systemic side effects, cost, ocular surface irritation, compliance, anddrop instillation. Because of these issues, patients essentially do not receive adequate therapy for their disease and are more likely to have disease progression associated with vision loss. Therefore, there is a significant need to create alternative techniques for drug delivery directly to the trabecular meshwork and Schlemm's canal. Retroject, Inc. is developing the disposable Retroject device to deliver various glaucoma drugs to these targeted sites. This proposal has two aims. In Aim 1, injections ofan FDA-approved drug will be injected into the eyes of human glaucoma patients using the Retroject device. IOP and aqueous humor outflow facility will be evaluated to determine the effect of the injection on these parameters. In Aim 2, safety and injection comfort will be assessed. The degree of safety will be assessed through a variety of means including the validated Patient Comfort Assessment Guide , corneal endothelial counts, corneal pachymetry, and thorough anterior and posterior segment clinical exams. The confirmation of safety and efficacy of the Retroject device in human glaucoma patients would provide significant support for its potential in glaucoma patient therapy. Successful achievement of these specific aims will ultimately lead to an STTR Phase II Proposal to not only enlarge the size of the clinical trial but also to assess a variety of glaucoma drugs with the Retroject device. Nanoparticles of various drugs which can release drug over 2-3 months will be injected into Schlemm's canal. Thiswould minimize the compliance issues associated with topical therapy and could significantly change the way we treat our glaucoma patients. PUBLIC HEALTH RELEVANCE PUBLIC HEALTH RELEVANCE: The vast majority of glaucoma patients are treated with topical therapy, however there are many inherent issues with this approach including noncompliance, cost, ocular surface irritation, and difficulty with drop instillation. The Retrojec device circumvents these issues by enabling drug delivery directly to the targeted site of resistance (Schlemm's canal). This can then provide more consistent lowering of intraocular pressure so fewer patients will lose vision from glaucoma.

* Information listed above is at the time of submission. *

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