Leveraging Standardized MRD Assays to Guide CLL Treatment2024-01-25T10:44:11-08:00January 25th, 2024|Read more
Clonal Characterization and Somatic Hypermutation Assessment by Next-Generation Sequencing in Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma2023-04-10T20:22:16-07:00March 23rd, 2023|Read more
DNA Sequencing to Detect Residual Disease in Adults With Acute Myeloid Leukemia Prior to Hematopoietic Cell Transplant2024-08-02T14:22:45-07:00March 7th, 2023|Read more
Minimal/Measurable Residual Disease (MRD) Monitoring in Patients with Lymphoid Neoplasms by High-Throughput Sequencing of the T-Cell Receptor2023-04-10T20:24:04-07:00March 2nd, 2023|Read more
Comparing Data Generated Using Multiparametric Flow Cytometry, Capillary Electrophoresis, and Next-Generation Sequencing in a Cohort of B-Cell Lymphoproliferative Disorder Samples2022-12-29T21:22:21-08:00November 15th, 2022|Read more
Invivoscribe Launches Grant Program to Support Novel Applications for Sequence-Based Analyses of the Immune System2025-08-26T08:18:25-07:00June 24th, 2021|Read more
Invivoscribe Premieres 12-Color Flow Cytometry Capabilities at their Reference Labs in the US, Europe, and China2026-03-09T18:08:11-07:00June 3rd, 2021|Read more
Invivoscribe Announces FDA Approval for Distribution of the LeukoStrat CDx FLT3 Mutation Assay as an IVD Kit in the United States2025-08-26T08:11:34-07:00May 19th, 2020|Read more
Invivoscribe Submits LeukoStrat® CDx FLT3 Mutation Assay to NMPA in China and Expands Company, Adding Laboratory in Shanghai to Provide Comprehensive Support for Partners.2021-02-26T19:10:05-08:00May 12th, 2020|Read more
The European Commission Approves Astellas’ XOSPATA® for Patients with Relapsed or Refractory Acute Myeloid Leukemia with a FLT3 Mutation Detected by Validated Tests, including the Invivoscribe LeukoStrat CDx FLT3 Mutation Assay2021-11-14T22:08:08-08:00December 5th, 2019|Read more