SBIR-STTR Award

Novel Nanosecond Laser and Ultrasound to Selectively Treat Eye Blood Vessels
Award last edited on: 1/22/2021

Sponsored Program
STTR
Awarding Agency
NIH : NEI
Total Award Amount
$225,000
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Yannis Mantas Paulus

Company Information

Photosonox LLC

600 South Wagner Road Suite 181
Ann Arbor, MI 48103

Research Institution

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Phase I

Contract Number: 1R41EY031219-01
Start Date: 6/1/2020    Completed: 5/31/2021
Phase I year
2020
Phase I Amount
$225,000
Wet age-related macular degeneration (AMD) is the leading cause of irreversible blindness in the developed world. Anti-VEGF therapy is currently the gold standard for wet AMD treatment. However, up to 50% of patients in the long term have a suboptimal response to anti-VEGF therapy. A better alternative method for treatment of AMD is urgently needed. We have recently invented a novel, effective, and highly-selective anti- vascular therapy, termed “photo-mediated ultrasound therapy (PUT)”. PUT is based on microcavitations in microvessels produced by synergistically applied laser pulses and ultrasound bursts. As demonstrated by our preliminary studies on clinically relevant animal models, PUT is capable of eliminating the target microvessels in the choroid without causing unwanted damage to the surround tissue, facilitating optimal treatment outcome for patients with AMD. The ultimate goal of our research is to develop and commercialize a new, noninvasive therapeutic technique for safe and efficient treatment of choroidal neovascularization (CNV) in patients with wet AMD. To achieve the ultimate goal, the project streamlines to achieve the technological transition, including the following milestones: (1) to build and verify the Phase I ?-prototype on rabbit eye models, (2) to build and verify the Phase II ?- prototype for human subjects, (3) to complete clinical studies, and (4) to define the approval pathway with the FDA. In this Phase I research, PhotoSonoX LLC, via an established collaboration with the Kellogg Eye Center at the University of Michigan School of Medicine, will build a clinically ready ?-prototype system, and fully test its safety and efficacy to pave the road to clinical studies in Phase II. The hypothesis of the Phase I study is that PUT can precisely remove pathologic microvessels in the eye without causing short-term and long-term damage in the surrounding tissue. To test this hypothesis, the following specific aims will be accomplished: Aim 1. Develop a clinically ready ?-prototype PUT system which has a reasonable cost and can be tested on clinically relevant rabbit eyes in Phase I and on human eyes in Phase II. Aim 2. Determine the long-term safety of PUT for treatment of choroidal microvessels on normal rabbits in vivo. Aim 3. Validate the short and long-term efficacy and safety of PUT for treating pathologic choroidal neovascularization in vivo on a rabbit model of AMD. The outcome from this research will be proof- of-concept that the PUT effectively and safely removes pathologic choroidal microvessels to treat AMD. We expect that the proposed PUT device has great potential to transform our care of patients with AMD by facilitating targeted and precise therapy while reducing the treatment burden and side effects.

Public Health Relevance Statement:
PROJECT NARRATIVE Photo-mediated ultrasound (PUT) therapy utilizes the synergistic application of nanosecond laser with ultrasound to create microcavitation bubbles which permanently shut down micro-size blood vessels based on photoacoustic cavitation without requiring any exogenous agent. This study determines the safety of PUT in treating the choroid and treating pathologic choroidal neovascularization mimicking macular degeneration in animal models. This study will develop a prototype for clinical translation of this technology.

Project Terms:
Age related macular degeneration; Angiography; Animal Model; Atrophic; base; Blindness; Blood; Blood Vessels; Cataract; Choroid; Choroid Diseases; Choroidal Neovascularization; Clinical; Clinical Research; clinical translation; clinically relevant; Collaborations; Contrast Media; cost; cost efficient; Data; Detection; Devices; Disease; Excision; experimental study; Eye; eye blood vessel; eye center; Feedback; Fundus photography; Glaucoma; Goals; Gold; Hemorrhage; Histopathology; Human; human subject; image guided; improved; in vivo; Infection; Injections; innovation; intravitreal injection; laser photocoagulation; Lasers; legally blind; Macular degeneration; Mediating; medical schools; Methods; Michigan; millisecond; Modeling; nanosecond; neovascularization; Neurons; neurosensory; Normal Cell; novel; Optics; optimal treatments; Oryctolagus cuniculus; Outcomes Research; particle; Pathologic; Pathologic Neovascularization; Pathway interactions; Patient Care; Patient-Focused Outcomes; Patients; Peripheral; Phase; phase 1 study; Photoreceptors; Photosensitization; Photosensitizing Agents; Physiologic pulse; proliferative diabetic retinopathy; prototype; real-time images; Research; response; Retina; retinal damage; Retinal Diseases; Safety; side effect; Signal Transduction; System; TdT-Mediated dUTP Nick End Labeling Assay; Techniques; Technology; Testing; Therapeutic; Time; Tissues; Ultrasonic Therapy; Ultrasonography; Universities; Vascular Endothelial Growth Factors; Vision; Work

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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