Real-world data on prognostic value of measurable residual disease assessment by fragment analysis or next-generation sequencing in multiple myeloma2022-09-07T22:22:23-07:00May 3rd, 2022|Read more
Ig Gene Clonality Analysis Using Next-Generation Sequencing for Improved Minimal Residual Disease Detection with Significant Prognostic Value in Multiple Myeloma Patients2022-01-06T05:38:03-08:00January 4th, 2022|Read more
NGS Analysis of Clonality and Minimal Residual Disease in a Patient with Concurrent Richter’s Transformation and CLL/SLL2022-01-08T23:37:03-08:00December 28th, 2021|Read more
Plan for a Successful International Drug Approval with Early Development of the Accompanying CDx2022-01-04T04:43:02-08:00December 8th, 2021|Read more
Machine Learning Algorithms Accelerate Throughput of a Flow – Sequencing Cell Based Assay for an Acute Myeloid Leukemia (AML) Therapeutic Discovery Platform2022-01-30T21:35:17-08:00November 5th, 2021|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