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