SBIR-STTR Award

High Z Oraya Therapy for Wet Amd
Award last edited on: 4/1/19

Sponsored Program
STTR
Awarding Agency
NIH : NEI
Total Award Amount
$215,200
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Erik William Chell

Company Information

Oraya Therapeutics Inc (AKA: GEM Biosystems Inc)

800 Jarvis Avenue Suite 200
Newark, CA 94560
   (510) 456-3700
   info@orayainc.com
   www.orayainc.com

Research Institution

Dana-Farber Cancer Institute

Phase I

Contract Number: 1R41EY024197-01
Start Date: 4/1/14    Completed: 3/31/15
Phase I year
2014
Phase I Amount
$215,200
The purpose of this project is to develop a new radiotherapy treatment modality that will substantially enhance the treatment of wet AMD with minimal toxicity to healthy tissue, leading to major improvement in visual acuity, decreased use of intravitreal injections of anti-VEGF agents, lower cost of treatment, and a substantially improved quality of life for patients. The new modality entitled "Customizable Radiotherapy Enhancement (CuRE)" using gold nanoparticles will enable major highly localized amplification of radiation damage to the neovascular AMD disease cells with minimal normal ocular tissue toxicity. In order to accomplish this, a potent amount of gold nanoparticles (AuNP), acting as "smart bombs" will be targeted specifically to the neovascular AMD (disease) endothelial cells (ECs) as demonstrated in published simulations by Harvard Medical School project partner. Once the AuNP home on to the disease ECs, a relatively small amount of radiation will be focused on the AuNP. The small radiation will induce (activate) the AuNP to emit electrons that will kill (blast) the disease cells with very minimal collateral damage and normal tissue toxicity. The radiation beam will be delivered using a recently developed radiotherapy device by the company project partner (Oraya Therapeutics Inc.) specifically suited for the treatment of neovascular AMD, but limited by normal tissue toxicity constraints. The use of AuNP as described above will circumvent these toxicity limitations enabling a potential breakthrough new treatment modality for neovascular AMD patients. The specific aims in phase I of the STTR, will establish feasibility of the new CuRE modality for circumventing these toxicity limitations during treatment. If Phase I is successful, Phase II will test the modality in preclinical (animal) models. If ultimately successful, the new Oraya CuRE approach could be extended beyond the treatment of wet AMD, as a novel approach for more effective highly targeted treatment of eye cancers: e.g. choroidal melanoma, whose endothelial cells can also be uniquely targeted by AuNP.

Public Health Relevance Statement:


Public Health Relevance:
The highest clinical significance of the new Oraya CuRE treatment modality is anticipated in achieving major reduction in the frequency/need of anti-VEGF injections for wet Age-related macular degeneration (AMD) patients with concomitant major improvement in visual acuity and quality of life. This highly targeted customizable treatment modality could become a highly effective treatment option for the millions of neovascular AMD patients in the U.S and around the world. If successful, the CuRE modality could be extended to enhance treatment efficacy for eye cancers e.g. retinoblastoma or choroidal melanoma.

Project Terms:
Age; Age related macular degeneration; Animal Model; Avastin; bevacizumab; Biodistribution; Biological; Biological Assay; Blast Cell; Blindness; Cells; Choroidal Neovascularization; Clinical Trials; clinically significant; combat; Contralateral; Data; design; Developed Countries; Development; Devices; Disease; Dose; Dose-Limiting; effective therapy; Electrons; Endothelial Cells; Ensure; Exudative age-related macular degeneration; Eye; fluorescence imaging; Frequencies (time pattern); Goals; Gold; Home environment; Image; improved; In Situ; In Vitro; in vivo; Incubated; Injection of therapeutic agent; intravitreal injection; Killings; laser photocoagulation; Lesion; malignant neoplasm of eye; Measures; medical schools; melanoma; minimal risk; Modality; Modeling; nanoparticle; neovascular; Normal tissue morphology; novel strategies; Optics; Outcome; Patients; Pharmaceutical Preparations; Phase; Photons; pre-clinical; programs; Property; public health relevance; Publishing; Quality of life; Radiation; Radiation therapy; Radiosurgery; Rattus; Residual state; Retinal Diseases; Retinoblastoma; Risk; Route; simulation; Small Business Technology Transfer Research; Software Tools; Testing; Therapeutic; Time; Tissues; Toxic effect; Treatment Cost; Treatment Efficacy; treatment planning; Visual Acuity

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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