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Skip to main content SISTER PUBLICATION LINKS * GenomeWeb * 360Dx * Precision Medicine Online * PMLS Events * RSS Feeds * Visit GenomeWeb on Twitter * Visit GenomeWeb on LinkedIn Premium Trial: Request an Annual Quote USER ACCOUNT MENU * My GenomeWeb * Profile * Newsletters * My Topics * Reading List * Log out Log in Subscribe Menu Close Menu MAIN NAVIGATION * My GenomeWeb * Profile * Newsletters * My Topics * Reading List * Log out * Business & Policy * Business News * Research Funding * Policy & Legislation * Regulatory News * Reimbursement * Technology * Microarrays & Multiplexing * PCR * Informatics * Sequencing * Mass Spec * Sample Prep * Gene Silencing/Gene Editing * Synthetic Biology * Spatial Biology * Research * Genetic Research * Gene Expression Research * Epigenetics Research * Proteomics & Protein Research * Cell Biology Research * Diagnostics * Molecular Diagnostics * Companion Diagnostics * Biomarker Discovery & Validation * Drug Discovery & Development * Clinical Sequencing * Liquid Biopsy * Disease Areas * Cancer * Infectious Disease * Cardiovascular Disease * Neurological & Psychological Disease * Autoimmune Disease * Inherited Disease * Reproductive Health * Respiratory * Gastrointestinal * COVID-19 * Applied Markets * Resources * Webinars * eCase Study Videos * The Scan * White Papers * Job Listings * New Products * People in the News * Genomics: Clinical Implementation * Advances in Clinical Genomics Profiling * Partner Content BREADCRUMB 1. Home 2. Business, Policy & Funding 3. Business News Premium Trial: Request an Annual Quote Log in Subscribe GENEDX, PROGNOS HEALTH PARTNER ON RARE DISEASE PATIENT DATA TO SHORTEN 'TREATMENT ODYSSEY' Jul 19, 2023 | staff reporter Save for later NEW YORK – GeneDx said Wednesday that it has formed a strategic partnership with Prognos Health to help the latter's life sciences clients suggest therapies for patients newly diagnosed with rare diseases. The firms hope to apply real-world genomic data to shorten what they called the "treatment odyssey." Under the partnership, New York-based Prognos will integrate de-identified whole-genome and whole-exome sequencing data from GeneDx into its Prognos Marketplace, where pharmaceutical companies, healthcare providers, and researchers can purchase custom patient cohorts. The partners hope that this combination will improve the ability to match newly diagnosed patients with US Food and Drug Administration-approved medications. "With the rare disease genomics data and expertise available to us through partners like GeneDx, our life science clients can leverage the Prognos Marketplace to bring about a paradigm shift in the treatment of rare diseases," Prognos Health CEO Sundeep Bhan said in a statement. "This partnership further enables us to provide actionable insights in rare disease that can help clinicians make more informed decisions and ensure patients receive the right treatment at the right time." Kareem Saad, chief transformation officer of Stamford, Connecticut-based GeneDx, said that its goal has always been to speed up diagnostics and treatment for patients. "This partnership gives us the opportunity to … connect clinicians and their patients with rare diseases to appropriate treatment options and ultimately improve health and health economic outcomes," he said. TO READ THE FULL STORY… Register for Free. …and receive Daily News bulletins. Already have a GenomeWeb or 360Dx account? Login Now FILED UNDER Business News Informatics Molecular Diagnostics North America collaboration rare disease Inherited Disease data integration GeneDx WE RECOMMEND 1. Rebranded GeneDx Bets Future on Whole-Exome, Whole-Genome Sequencing in Pediatric Rare Disease Neil Versel, GenomeWeb, 2023 2. Dante Genomics, TMA Precision Health Partner for Rare Disease Diagnostics staff reporter, GenomeWeb, 2022 3. Illumina, Henry Ford Health Partner on Genomic Testing for Cardiovascular Patients staff reporter, GenomeWeb, 2023 4. Centogene to Offer Rare, Neurodegenerative Genomic Data for Rare Neurodegenerative Diseases on BC Platforms Network staff reporter, GenomeWeb, 2022 1. Centogene to Offer Genomic Data for Rare Neurodegenerative Diseases on BC Platforms Network staff reporter, GenomeWeb, 2022 2. Illumina, Genetic Alliance Launch $120M Global Whole-Genome Sequencing Program staff reporter, GenomeWeb, 2021 3. Genomenon Partners With Neurodevelopmental Disease Groups on Drug Development staff reporter, GenomeWeb, 2022 4. Broad Institute Launches $1K Sample-to-Report Clinical Whole-Genome Sequencing Service Huanjia Zhang, GenomeWeb, 2023 Powered by * Privacy policy * Do not sell my personal information * Google Analytics settings I consent to the use of Google Analytics and related cookies across the TrendMD network (widget, website, blog). Learn more Yes No Breaking News * 23ANDME LAYS OFF 71 THERAPEUTICS-RELATED EMPLOYEES AS GSK PARTNERSHIP ENDS AND Q1 REVENUES SLIDE * QIAGEN REPORTS 9 PERCENT NON-COVID SALES GROWTH IN Q2, CUTS FULL-YEAR GUIDANCE * VERACYTE Q2 SALES UP 24 PERCENT, DRIVEN BY PROSTATE AND THYROID CANCER TESTS * INVITAE Q2 REVENUES FALL 12 PERCENT AS FIRM LOWERS FULL-YEAR GUIDANCE * SEER Q2 REVENUES UP 11 PERCENT, CUTS 2023 GUIDANCE BY ROUGHLY A THIRD The Scan ANALYSIS OF NEW DRUG APPROVALS SUGGESTS RELIANCE ON LESS RIGOROUS STANDARDS In JAMA Network Open, researchers examine FDA's novel drug approval data to find a trend toward less rigorous standards in drug approvals. GWAS IDENTIFIES LOCI LINKED TO BINGE EATING DISORDER In a genome-wide association study appearing in Nature Genetics, researchers home in on three loci tied to binge eating disorder. BLOOD DNA METHYLATION-BASED ASSAY FOR EARLY DIAGNOSIS OF BREAST CANCER In Nature Communications, researchers describe a new assay that uses differences in DNA methylation patterns to distinguish breast cancer patients and controls. EQTL STUDY UNCOVERS NEW CANDIDATE GENES FOR ADIPOSE TISSUE BIOLOGY In BMC Genomics, researchers report that a study of Greek individuals uncovered additional genes with cis-eQTLs in adipose tissue. What's Popular? 1. PACIFIC BIOSCIENCES, GENEDX, UW COLLABORATE ON GOOGLE-FUNDED STUDY OF WGS IN NEONATAL CARE 2. DISTRICT COURT ISSUES INJUNCTION PROHIBITING FALSE ADVERTISING IN NATERA-CAREDX LEGAL ROW 3. PREPRINT CASTS DOUBT ON STUDY UNDERPINNING MICROBIOME-BASED CANCER DX TEST FROM MICRONOMA PREMIUM 4. QUANTUM-SI EXPERIENCING BUMPY ROLLOUT OF PLATINUM PROTEOMICS SYSTEM PREMIUM 5. PACIFIC BIOSCIENCES TO BUILD 'HIGH-THROUGHPUT ONSO' FOLLOWING $110M APTON BIOSYSTEMS ACQUISITION PREMIUM SPONSORSHIPS FOOTER * About us * Advertise * Contact * FAQ * Jobs * Sitemap * Submit a Tip Subscribe Privacy Policy. Terms & Conditions. Copyright © 2023 GenomeWeb, a business unit of Crain Communications. All Rights Reserved. Our site uses cookies and related technologies, as described in our Datenschutzerklärung, for purposes that may include site operation, analytics, enhanced user experience, or advertising. You may choose to consent to our use of these technologies or manage your own preferences. Akzeptieren Ablehnen Einstellungen verwalten