Measurable Residual Disease detection in acute lymphoblastic leukaemia – comparison between targeted NGS and ASO-qPCR2026-07-09T17:00:41-07:00January 23rd, 2026|Read more
Measurable residual disease monitoring after hematopoietic stem cell transplantation2026-07-06T16:26:02-07:00December 30th, 2025|Read more
Measurable residual mutated NPM1 before allogeneic transplant for acute myeloid leukemia2025-11-24T09:51:38-08:00November 24th, 2025|Read more
QuANTUM-First: Clinical Validation of the LeukoStrat Companion Diagnostic for the Selection of Patients With Acute Myeloid Leukemia Harboring FMS-Like Tyrosine Kinase 3–Internal Tandem Duplications for Treatment With Quizartinib2026-04-20T09:03:35-07:00September 3rd, 2025|Read more
A Systematic, Evidence-Based Workflow for Classifying KMT2A Fusions in AML2026-04-20T09:01:54-07:00July 29th, 2025|Read more
Invivoscribe’s LabPMM Gains New York State Approval for the FLT3 ITD MRD Assay2026-03-09T18:44:44-07:00April 22nd, 2025|Read more
Invivoscribe Announces Registration of the LeukoStrat® CDx FLT3 Mutation Assay in the United Kingdom and Switzerland2026-03-09T18:48:48-07:00March 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 EEA2024-10-08T03:14:44-07:00October 8th, 2024|Read more
Study Suggests Critical Link Between Residual FLT3-ITD Mutations in Remission and Post-Transplant Outcomes in AML2026-03-09T18:43:04-07:00May 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 VANFLYTA2025-08-26T07:35:25-07:00July 21st, 2023|Read more
The 66th Annual Meeting of the Japanese Society of Lymphoma Research Jun 4 – 6, 2026Â Tokyo, Japan Attending