SBIR/STTR Research Award

Topical Eyedrop Therapy for Keratoconus

Award identifier 208f31528079d9a832a8aba0fd189d285aaf45c94ba87faf74057f3c0bda4bc1Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$1,680,476

Program and phase

SBIR · Phase II – Direct to Phase II

Award year

2020

Explore This Research Award in CaptureIQ

Research the technology, evaluate the recipient and agency, identify related opportunities, and explore potential follow-on work with CaptureIQ.

Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Iveena Delivery Systems, Inc.
Proposal award date
2020-09-01
Contract end date
2022-08-31
UEI
EQ3KNDP93M27
Solicitation number
PA19-272
Topic code
NEI

Research abstract

Project Summary Keratoconus (KCN) is a corneal disorder in which the central portion of the cornea becomes thinner and bulges forward in a cone-shaped fashion resulting in myopia, irregular astigmatism, and eventually visual impairment. The earliest signs of keratoconus are usually blurred vision and frequent changes in eye glass prescription, or vision that cannot be corrected with glasses. Symptoms of keratoconus generally begin in the late teenage years or early twenties, but can start at any time. Treatment options are surprisingly limited with no oral or topical pharmaceutical therapy. Most mild KCN can be corrected with glasses or soft contact lenses but very often patients will need toric or hard contacts as the disease progresses. Ultimately, 1 in 5 patients will require surgery, such as corneal transplant or UV-A crosslinking, which poses significant risks of scarring, visual haze, fluctuation, and pain. Our technology, IVMED-80 eye drops, is based on a co-factor for lysyl oxidase (LOX) activity. Deficient LOX activity in the cornea has been linked to the development of keratoconus both genetically and biochemically. Using Phase 1 funding support, we were able to restore lysyl oxidase activity in human corneal fibroblasts from keratoconic corneas and increase levels of crosslinked collagen as measured by lysylnorleucine in rabbit eyes. We demonstrated topical therapy increased biomechanical strength of human cadaver corneas and rabbit corneas as measured by both extensiometry ex vivo and waveform deformation analysis in vivo. Finally, topical copper therapy induced flattening of the rabbit cornea comparable to levels observed with conventional surgical crosslinking in humans. This body of data resulted in iVeena being granted orphan designation for IVMED- 80. In this Phase 2 SBIR project, we propose experiments that will enable us to submit an IND and start a US clinical trial. We propose to analyze optimal duration of therapy and potential risk of relapse after different durations of treatment, manufacture a GMP batch with stability testing according to ICH guidelines, and perform a 6-month GLP toxicology study in rabbits.Project Narrative Keratoconus is a progressive corneal thinning disorder that compromises vision, is usually bilateral, and is the leading cause of full-thickness corneal transplantation in the US. The most recent treatment for keratoconus, UV-A assisted surgical crosslinking, poses significant risks of infection, scarring, haze, visual fluctuation, and pain; there is no pharmacologic treatment as yet for this debilitating, vision-threatening disorder. iVeena is developing a new topical eyedrop therapy for keratoconus which works by enhancing physiological corneal crosslinking through increasing lysyl oxidase activity, without the need for light or surgery.

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

7 SBIR/STTR records share this UEI (2015–2025). Reported award amounts total $5,630,748. Reported amounts are not federal obligations.

Phases: Phase I, Phase II, Phase II – Direct to Phase II

Agencies: Department of Health and Human Services, National Science Foundation

Agency intelligence

Department of Health and Human Services

Back to SBIR/STTR Research Awards

Don't take our word for it. Ask AI about RFPCapture.

See what leading AI assistants have to say about RFPCapture and CaptureIQ.

Gemini opens without a prefilled question. The question is copied to your clipboard when the button works. You can also copy it here:

What is RFPCapture.com and its CaptureIQ platform from Smart Logic AI? How does it help federal contractors discover opportunities, evaluate bid/no-bid decisions, research government contracts, and prepare proposals? How does it compare with other federal capture platforms? Use independent sources where available.