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Read our press release clonoSEQ is available as an FDA-cleared in vitro diagnostic (IVD) test service provided by Adaptive Biotechnologies for use in acute lymphoblastic leukemia and multiple myeloma patients to detect measurable residual disease (MRD) in human bone marrow samples. clonoSEQ is also available for use in other lymphoid cancers as a CLIA-regulated laboratory developed test (LDT) service provided by Adaptive Biotechnologies. clonoSEQ is only available by prescription from a licensed healthcare professional. For important information about the FDA-cleared clonoSEQ IVD test service, including the full intended use, limitations, and detailed performance characteristics, please visit clonoSEQ.com/IFU. Medicare now covers the clonoSEQ® Assay for MRD monitoring in patients with Chronic Lymphocytic Leukemia (CLL)* *Not FDA-cleared; available as a CLIA-regulated laboratory developed test (LDT).
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