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Sebia Receives U.S. FDA Clearance for the FLC Kappa & Lambda Assays

Sebia Receives U.S. FDA Clearance for the FLC Kappa & Lambda Assays
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Sebia Receives U.S. FDA Clearance for the FLC Kappa & Lambda Assays

Sebia, a global specialty diagnostic company providing innovative solutions for screening and diagnostics in oncology, metabolic diseases, genetic disorders and autoimmune diseases, today announced that it has received 510(k) clearance from the U.S..

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Immix Biopharma Announces Complete Response in 9th Relapsed/Refractory AL Amyloidosis Patient in NXC-201 Clinical Trial at IMS 20th Annual Meeting

100% overall response rate and 67% complete response rate observed in heavily pre-treated patients with daratumumab relapsed/refractory AL Amyloidosis as of the September 20, 2023 data cutoff100% .

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