Comparison of Complete Genomics DNBSEQ-G99 Sequencer and Illumina® MiSeqTM using Invivoscribe’s FLT3 ITD MRD Assay and NPM1 MRD Assaywmm2025-03-18T17:44:25-07:00November 8th, 2024|Read more
Performance Comparison of Invivoscribe’s LymphoTrack® Assays Between Complete Genomics DNBSEQ-G99 and Illumina® MiSeqTM NGS Platformswmm2025-03-18T17:44:43-07:00November 8th, 2024|Read more
Clonality and Measurable Residual Disease (MRD) Testing on the Illumina NextSeq SequencersInvivoscribe Marketing2024-06-21T12:55:12-07:00June 21st, 2024|Read more
Measurable Residual FLT3 Internal Tandem Duplication Before Allogeneic Transplant for Acute Myeloid LeukemiaInvivoscribe Marketing2024-05-02T11:47:00-07:00May 2nd, 2024|Read more
Assessment of Bone Marrow Involvement in B-Cell non-Hodgkin Lymphoma Using Immunoglobulin Gene Rearrangement Analysis with Next-Generation SequencingInvivoscribe Marketing2024-03-26T13:55:01-07:00March 20th, 2024|Read more
Invivoscribe Announces Registration of the LeukoStrat® CDx FLT3 Mutation Assay in the United Kingdom and SwitzerlandInvivoscribe Marketing2025-03-28T10:05:45-07:00March 27th, 2025|Read more
EU Notified Body (BSI Netherlands) and the EMA Grant Approval of the LeukoStrat® CDx FLT3 Mutation Assay for VANFLYTA® Therapy in the EU and EEAwmm2024-10-08T03:14:44-07:00October 8th, 2024|Read more
Study Suggests Critical Link Between Residual FLT3-ITD Mutations in Remission and Post-Transplant Outcomes in AMLInvivoscribe Marketing2024-05-07T17:44:56-07:00May 8th, 2024|Read more
Invivoscribe Announces FDA Approval of the LeukoStrat CDx FLT3 Mutation Assay to Select Patients with FLT3-ITD Positive AML for Treatment with VANFLYTAInvivoscribe Marketing2023-07-20T17:27:41-07:00July 21st, 2023|Read more
Invivoscribe Partners with Complete Genomics to Develop and Commercialize Biomarker Tests for Oncology and Cancer ResearchInvivoscribe Marketing2023-06-05T12:37:16-07:00June 2nd, 2023|Read more