Aditxt Subsidiary Pearsanta Seeks Clinical Trial Translational Endpoints Research Award for Early Detection of Ovarian Cancer

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Ovarian Cancer Diagnostic Market Growth: Projected Increase from $1.5 Billion in 2023 to $2.7 Billion by 20321 Amidst Current Challenges of Insufficiently Sensitive Blood Tests for Early Detection

MOUNTAIN VIEW, Calif., August 07, 2024--(BUSINESS WIRE)--Aditxt, Inc. ("Aditxt") (NASDAQ: ADTX), a company dedicated to discovering, developing, and deploying promising health innovations, announced that its subsidiary, Pearsanta, Inc. ("Pearsanta") has submitted a proposal for the Clinical Trial Translational Endpoints Research Award to the Congressionally Directed Medical Research Programs (CDMRP) of the Department of Defense. The proposal aims to validate a novel assay based on Pearsanta’s proprietary Mitomic? Technology for the early detection of ovarian cancer.

According to the World Ovarian Cancer Coalition, ovarian cancer remains a significant health concern, with over 324,603 new cases diagnosed worldwide in 2022. It is the 18th most common cancer globally and the 8th most common among women, according to the World Cancer Research Fund International. The lifetime risk for a woman being diagnosed with ovarian cancer is approximately 1 in 87, while the risk of dying from invasive ovarian cancer is about 1 in 130, based on information provided by the American Cancer Society. According to the Ovarian Cancer Research Alliance, the five-year relative survival rate for ovarian cancer stands at around 50.8%. Despite the prevalence of this cancer, Pearsanta does not believe that any blood tests are currently available with adequate sensitivity for early detection of ovarian cancer, underscoring a critical need for improved diagnostic methods?.

Pearsanta’s Mitomic Technology Platform seeks to harness the unique properties of mitochondrial DNA (mtDNA) to detect disease through non-invasive, blood-based liquid biopsies. This platform is designed to identify specific mutations in mtDNA indicative of various diseases. Due to its high mutation rate and cell persistence, Pearsanta believes mtDNA is an excellent biomarker for early disease detection. This platform allows for the rapid and accurate identification of disease-associated biomarkers, significantly enhancing early diagnosis and treatment. Currently, the program focuses on developing tests for early cancer detection, targeting ovarian, prostate, and lung cancers, and addressing non-cancerous conditions like endometriosis.

Pearsanta’s proposal to CDMRP focuses on validating the Mitomic Ovarian Test (MOT), which utilizes mtDNA mutations as early indicators of ovarian cancer. The application of mtDNA technology to detect ovarian cancer in servicewomen could potentially also transition to US public health funding agencies such as BARDA, showcasing the significant potential for widespread public health utilization. The objective is to create a reliable blood test that can detect ovarian cancer at its earliest stages, which has the potential to improve treatment outcomes and survival rates significantly. In response to the CDMRP’s Clinical Trial Translational Endpoints Research Award, the Pearsanta team has designed a prospective cohort study collecting blood samples and clinical information from patients undergoing surgery to diagnose ovarian cancer. Follow-up surgical reports identify the tumor’s presence, type, and stage. The study will enroll 100 subjects with ovarian cancer and 200 negative controls. The control group will include both symptomatic patients with no detected cancer and asymptomatic patients, some of whom have a history of other gynecologic cancers, breast cancer, or endometriosis. The study is powered to detect significant diagnostic accuracy (AUC > 0.85) at each stage of epithelial ovarian cancer vs. controls and non-epithelial cancer vs. controls.