CENTOGENE, a commercial-stage company focused on rare diseases that transforms real-world clinical and genetic data into actionable information for patients, physicians and pharmaceutical companies, has a new data access and collaboration agreement with Pfizer Inc. The agreement grants Pfizer access to CENTOGENE’s data repository, which may be used in the discovery and validation of novel genetic and biochemical targets for the potential development of new therapies for rare diseases.
Founded in 2006, headquartered in Rostock, Germany, Centogene’s goal is to bring rationality to treatment decisions and to accelerate the development of new orphan drugs by using knowledge of the global rare disease market, including epidemiological and clinical data and innovative biomarkers. Centogene has developed a global proprietary rare disease platform based on a real-world data repository with over 2.0 billion weighted data points from over 450,000 patients representing 115 different countries as of August 31, 2019, or an average of over 500 data points per patient.
Founded in 1848, headquartered in New York, Pfizer is a leading research-based biopharmaceutical company. They apply science and global resources to deliver innovative therapies that extend and significantly improve lives.
Under the terms of the agreement, CENTOGENE and Pfizer will work together to mine the data repository and jointly agree to any collaborative research projects designed to substantiate results of data mining. CENTOGENE will receive an upfront payment and will be eligible for additional research payments under any future collaborative research projects. Individual-level data from the repository will be managed, protected and shared with Pfizer in compliance with international data privacy regulations.
CENTOGENE’s rare disease data repository integrates relevant structured and unstructured patient data, including clinical information; health records; and genetic, transcriptomic, proteomic, and metabolomic data. It also includes longitudinal data such as biomarker or patient recorded outcome, as well as diagnostic workflow data.
“With what we believe to be the world’s largest data repository of epidemiologic, phenotypic and clinical data in orphan diseases, CENTOGENE is fuelling the global knowledge base of rare disease patient populations.” … “The potential for furthering the understanding of rare disease is extremely important for patients around the world, and we hope that today’s collaboration agreement will help lead to better diagnosis and potential treatments for patients with rare diseases.” – Arndt Rolfs, CEO of CENTOGENE