Helix, a prominent population genomics company, is unveiling clinico-genomic datasets aimed at empowering life science firms in advancing precision medicine drug discovery and development. These datasets, meticulously constructed through Helix's extensive collaborations with health systems, encompass comprehensive longitudinal clinical and genomic records spanning diverse therapeutic domains, including Cardiovascular, Immunology & Inflammation, and Metabolic conditions.
Hylton Kalvaria, Chief Commercial Officer of Helix, highlights the significance of these resources, emphasizing their potential for elucidating genetic determinants of disease progression and clinical outcomes, as well as for validating therapeutic candidates. Moreover, organizations can swiftly pinpoint targeted patient cohorts based on specific genetic and phenotypic criteria, enhancing the efficiency of discovery and clinical development endeavors.
Helix's precision cohorts amalgamate longitudinal clinical data with the company's proprietary Exome+® sequencing data from over 125,000 consented patients across the US, with regular data updates. Partners gain access to structured Electronic Health Record (EHR) fields, encompassing clinical diagnoses, procedures, lab results, and prescriptions. For instance, the newly introduced Cardiometabolic cohort comprises over 50,000 patients with significant Cardiovascular Disease diagnoses, alongside vital patient demographics and key lab metrics like triglycerides and cholesterol, all intricately linked to exome sequencing data covering pertinent Cardiovascular genes.
James Lu, M.D., Ph.D., CEO and co-founder of Helix, underscores the transformative potential of clinico-genomic data in driving the development of targeted therapeutics with enhanced safety and efficacy profiles. Leveraging real-world data and genomics, precision medicine holds the promise of revolutionizing drug development, ushering in an era of personalized treatment paradigms.