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Friday, April 12th, the #𝐅𝐃𝐀’𝐬 𝐎𝐧𝐜𝐨𝐥𝐨𝐠𝐢𝐜 𝐃𝐫𝐮𝐠𝐬 𝐀𝐝𝐯𝐢𝐬𝐨𝐫𝐲 𝐂𝐨𝐦𝐦𝐢𝐭𝐭𝐞𝐞 𝐯𝐨𝐭𝐞𝐝 𝟏𝟐 𝐭𝐨 𝟎 𝐭𝐡𝐚𝐭 𝐭𝐡𝐞 𝐭𝐨𝐭𝐚𝐥𝐢𝐭𝐲 𝐨𝐟 𝐚𝐯𝐚𝐢𝐥𝐚𝐛𝐥𝐞 𝐝𝐚𝐭𝐚 𝐬𝐮𝐩𝐩𝐨𝐫𝐭𝐬 𝐭𝐡𝐞 𝐮𝐬𝐞 𝐨𝐟 𝐦𝐢𝐧𝐢𝐦𝐚𝐥 𝐫𝐞𝐬𝐢𝐝𝐮𝐚𝐥 𝐝𝐢𝐬𝐞𝐚𝐬𝐞 (#𝐌𝐑𝐃) 𝐚𝐬 𝐚𝐧 𝐞𝐧𝐝 𝐩𝐨𝐢𝐧𝐭 𝐟𝐨𝐫 𝐚𝐜𝐜𝐞𝐥𝐞𝐫𝐚𝐭𝐞𝐝 𝐚𝐩𝐩𝐫𝐨𝐯𝐚𝐥 𝐨𝐟 𝐧𝐞𝐰 𝐭𝐫𝐞𝐚𝐭𝐦𝐞𝐧𝐭𝐬 𝐟𝐨𝐫 𝐩𝐚𝐭𝐢𝐞𝐧𝐭𝐬 𝐰𝐢𝐭𝐡 𝐦𝐮𝐥𝐭𝐢𝐩𝐥𝐞 #𝐦𝐲𝐞𝐥𝐨𝐦𝐚. Sebia’s CEO, Jean Marc Chermette touts, “This is a tremendous advance for patients with multiple myeloma, enabling investigators and biopharma companies to get much needed new promising agents made available and accessible. MRD plays a major role in the care of myeloma patients and having an analytically validated blood-based MRD assay such as M-inSight will serve a crucial need and spare having to perform for bone marrow biopsies”. #Sebia congratulates Representatives from The University of Miami’s Sylvester Comprehensive Cancer Center and the i2TEAMM who presented three independent data sets from a meta-analysis based on patient-level data from several clinical trials. The level of rigor of these analyses are superb and sets a new standard for biomarker development in oncology. ➡️ Visit https://lnkd.in/eXd5eNkT to learn more about M-inSight! #Minimalresidualdisease #Multiplemyeloma #MinSight

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Discover M-inSight!

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