Performance Comparison of Illumina® MiSeq™ and MiSeq™ i100 Systems using Invivoscribe’s LymphoTrack® Assays 2026-04-20T09:00:11-07:00May 27th, 2025| Read more
From prognostication to precision in acute myeloid leukemia 2025-05-08T16:47:49-07:00May 8th, 2025| Read more
Measurable residual disease and post-transplantation gilteritinib maintenance for patients with FLT3 ITD mutated AML 2025-05-09T09:20:30-07:00May 8th, 2025| Read more
Comparison of Complete Genomics DNBSEQ-G99 Sequencer and Illumina® MiSeqTM using Invivoscribe’s FLT3 ITD MRD Assay and NPM1 MRD Assay 2026-01-07T13:13:14-08:00November 8th, 2024| Read more
Performance Comparison of Invivoscribe’s LymphoTrack® Assays Between Complete Genomics DNBSEQ-G99 and Illumina® MiSeqTM NGS Platforms 2026-04-20T09:02:18-07:00November 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 VANFLYTA 2025-08-26T07:35:25-07:00July 21st, 2023| Read more
Invivoscribe Partners with Complete Genomics to Develop and Commercialize Biomarker Tests for Oncology and Cancer Research 2025-12-19T18:08:11-08:00June 2nd, 2023| Read more
Invivoscribe Announces Updated Reimbursement for the LeukoStrat CDx FLT3 Mutation Assay to Select Newly Diagnosed FLT3-ITD Positive AML Patients Eligible for VANFLYTA in Japan 2025-12-29T12:29:29-08:00May 25th, 2023| Read more
Invivoscribe Announces IVDR Approval of the LeukoStrat CDx FLT3 Mutation Assay 2023-05-11T03:12:47-07:00May 11th, 2023| Read more
Invivoscribe Diagnostic Technologies (Shanghai) Co. Ltd. Receives CAP Accreditation to Support Clinical Research Testing for Pharmaceutical Partners in China 2023-02-23T06:28:40-08:00February 23rd, 2023| Read more
The 30th Annual Meeting of Japanese Association for Molecular Target Therapy of Cancer Jun 30 – Jul 2, 2026 Hiroshima, Japan Attending