RetinalGeniX Technologies, Inc. Nears Completion of Institutional Review Board for Research on DNA/GPS Program - Seite 2

Safe Harbor Statement

This press release contains certain forward-looking statements within the meaning of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. These statements are identified by the use of the words “could,” “believe,” “anticipate,” “intend,” “estimate,” “expect,” “may,” “continue,” “predict,” “potential,” “project” and similar expressions that are intended to identify forward-looking statements and include statements regarding the Company nearing completion of an Institutional Review Board for research on its DNA/GPS program, the study identifying hematology biomarkers that may help personalize medical evaluations for patients undergoing treatments for macular degeneration, the study offering recommendations for enhancing the management of ocular injections, conducting the study on 100 patients to establish standards for determining effective and ineffective eye injections for treating macular degeneration, following global standards for ophthalmology research to ensure that the resulting biomarkers can be universally applied, the study helping in better management of the condition, leading the collaborative study among leading universities to identify hematology biomarkers, being able to personalize medical evaluations for patients receiving treatment for macular degeneration, 200 million people worldwide having AMD, the number people worldwide having AMD rising to close to 300 million by 2040, developing technologies to screen, monitor, diagnose, and treat ocular, optical, and sight-threatening disorders, preventing vision loss and blindness due to diabetic retinopathy and maculopathy through early detection, DNA/GPS having the ability to screen, monitor, and provide data to profile, trend and create diagnostic markers for systemic and retinal disorders i.e., cardiovascular, Alzheimer's, Parkinsonism, and other diseases and the markers and data analysis being rapid and cost-effective and eliminating the need for expensive diagnostic equipment such as MRIs and CT scanning in many cases. These forward-looking statements are based on management’s expectations and assumptions as of the date of this press release and are subject to a number of risks and uncertainties, many of which are difficult to predict, that could cause actual results to differ materially from current expectations and assumptions from those set forth or implied by any forward-looking statements. Important factors that could cause actual results to differ materially from current expectations include, among others, the Company’s ability to complete an Institutional Review Board for research on its DNA/GPS program and conduct a study identifying hematology biomarkers that may help personalize medical evaluations for patients undergoing treatments for macular degeneration as planned, the Company’s ability to develop technologies to screen, monitor, diagnose, and treat ocular, optical, and sight-threatening disorders, preventing vision loss and blindness due to diabetic retinopathy and maculopathy through early detection, the ability of DNA/GPS to screen, monitor, and provide data to profile, trend and create diagnostic markers for systemic and retinal disorders i.e., cardiovascular, Alzheimer's, Parkinsonism, and other diseases, the ability of the Company’s data analysis to eliminate the need for expensive diagnostic equipment such as MRIs and CT scanning in many cases, and the risk factors described in the Company’s Annual Report on Form 10-K for the year ended December 31, 2022 and the Company’s subsequent filings with the SEC, including subsequent periodic reports on Forms 10-Q and 8-K. The information in this release is provided only as of the date of this release, and we undertake no obligation to update any forward-looking statements contained in this release on account of new information, future events, or otherwise, except as required by law.