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SOPHiA GENETICS Announces Expansion of Work with CHU de Nîmes

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SOPHiA GENETICS (Nasdaq: SOPH) announces expanded research partnership with CHU de Nîmes, a regional and university hospital in France. CHU de Nîmes will utilize SOPHiA DDM™ Platform for pharmacogenomics research, aiming to personalize medication response based on genetic profiles.
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Through the expanded relationship CHU de Nîmes will advance its research of rare and inherited diseases through pharmacogenomics

BOSTON and ROLLE, Switzerland, Nov. 30, 2023 /PRNewswire/ -- SOPHiA GENETICS (Nasdaq: SOPH), a cloud-native software company and a leader in data-driven medicine, today announced that it has expanded its work with CHU de Nîmes, a regional and university hospital located in the South of France. The hospital system will use the SOPHiA DDM™ Platform to progress its pharmacogenomics research.

Pharmacogenomics research is a field of research that looks at how an individual's unique genetic profile can affect response to medications, with the long-term goal to support clinicians in their choice of drugs and doses to best treat their patients.

"As precision medicine continues to become the gold standard of care, it's essential that hospitals and organizations like CHU de Nîmes have access to technologies to help streamline research and treatment planning, starting with identifying how an individual's genetic profile influences response to a certain medication" said Kevin Puylaert, Managing Director, EMEA, SOPHiA GENETICS. "With the SOPHiA DDM™ Platform, CHU de Nîmes will be able to advance its pharmacogenomics work, with the aim to bring about a broader use of personalized treatment plans for the French patient population."

CHU de Nîmes is a member of the French-speaking group RNPGx, an international organization of some of the top researchers in the field of pharmacogenomics. RNPGx aims to further the adoption and implementation of pharmacogenetics testing.

Top researchers from RNPGx member institutions collaborated with SOPHiA GENETICS to develop a pharmacogenomics panel. The panel is a targeted, capture-based NGS panel that will expedite the process of testing and accelerate pharmacogenomics research.  Additionally, the analytical capabilities of the SOPHiA DDM ™ Platform provide CHU de Nîmes with streamlined insights to facilitate fast and accurate variant discovery and reporting.

CHU de Nîmes also uses SOPHiA GENETICS' technology for its research and treatment planning for autism and research of blood cancers. With the expanded relationship, CHU de Nîmes will continue to retain ownership of its research database, building upon the work already done through its use of SOPHiA GENETICS and helping increase the team's expertise in a variety of research areas.

For more information, visit SOPHiAGENETICS.COM, or connect on X, LinkedIn, Facebook, and Instagram

About SOPHiA GENETICS 
SOPHiA GENETICS (Nasdaq: SOPH) is a software company dedicated to establishing the practice of data-driven medicine as the standard of care and for life sciences research. It is the creator of the SOPHiA DDM™ Platform, a cloud-native platform capable of analyzing data and generating insights from complex multimodal data sets and different diagnostic modalities. The SOPHiA DDM™ Platform and related solutions, products and services are currently used by a broad network of hospital, laboratory, and biopharma institutions globally. For more information, visit SOPHiAGENETICS.COM, or connect on X, LinkedIn, Facebook, and Instagram. Where others see data, we see answers. 

SOPHiA GENETICS products are for Research Use Only and not for use in diagnostic procedures unless specified otherwise. The information in this press release is about products that may or may not be available in different countries and, if applicable, may or may not have received approval or market clearance by a governmental regulatory body for different indications for use. Please contact support@sophiagenetics.com to obtain the appropriate product information for your country of residence.

SOPHiA GENETICS Forward-Looking Statements:
This press release contains statements that constitute forward-looking statements. All statements other than statements of historical facts contained in this press release, including statements regarding our future results of operations and financial position, business strategy, products, and technology, as well as plans and objectives of management for future operations, are forward-looking statements. Forward-looking statements are based on our management's beliefs and assumptions and on information currently available to our management. Such statements are subject to risks and uncertainties, and actual results may differ materially from those expressed or implied in the forward-looking statements due to various factors, including those described in our filings with the U.S. Securities and Exchange Commission. No assurance can be given that such future results will be achieved. Such forward-looking statements contained in this press release speak only as of the date hereof. We expressly disclaim any obligation or undertaking to update these forward-looking statements contained in this press release to reflect any change in our expectations or any change in events, conditions, or circumstances on which such statements are based, unless required to do so by applicable law. No representations or warranties (expressed or implied) are made about the accuracy of any such forward-looking statements.

 

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SOURCE SOPHiA GENETICS

FAQ

What is the latest announcement from SOPHiA GENETICS (SOPH) regarding CHU de Nîmes?

SOPHiA GENETICS (Nasdaq: SOPH) has expanded its work with CHU de Nîmes, a regional and university hospital in the South of France, to advance its research of rare and inherited diseases through pharmacogenomics.

What is the SOPHiA DDM™ Platform and how will CHU de Nîmes use it?

The SOPHiA DDM™ Platform is a cloud-native software that analyzes an individual's unique genetic profile to understand how it affects their response to medications. CHU de Nîmes will use this platform to progress its pharmacogenomics research.

What is the goal of pharmacogenomics research?

Pharmacogenomics research aims to study how an individual's genetic profile can influence their response to medications, with the long-term goal of supporting clinicians in choosing the most effective drugs and doses for their patients.

Who is Kevin Puylaert and what is his role in the announcement?

Kevin Puylaert is the Managing Director, EMEA, at SOPHiA GENETICS. He emphasized the importance of hospitals like CHU de Nîmes having access to technologies like the SOPHiA DDM™ Platform to streamline research and treatment planning.

What is the significance of this partnership for SOPHiA GENETICS (SOPH) and CHU de Nîmes?

This partnership signifies SOPHiA GENETICS' commitment to advancing data-driven medicine and CHU de Nîmes' dedication to personalized treatment through pharmacogenomics research.

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About SOPH

sophia genetics, world's largest clinical genomics community, brings together expertise in genetics, bioinformatics, machine learning and genomic privacy. based in switzerland, we are known for our high medical standards and swiss precision. sophia genetics offers health professionals who perform clinical genetic testing unparalleled bioinformatics analysis, quality assurance and secure banking of patient dna sequence data generated by ngs. the company helps clinical laboratories to reduce costs, overcome complexity, significantly improve the turnaround time for routine diagnosis and meet quality requirements related to the use of ngs in the clinic. our solution, the sophia ddm™ platform allows hospitals to better and faster diagnose patients using cutting edge ngs analytics algorithms and through knowledge sharing within the largest clinical genomics community in the world (+100 hospitals). the name « sophia » means wisdom in greek and it is the definition of our excellence based