Plasma Cell Myeloma Residual Disease Quantitation Using a Next-Generation Sequencing-Based IGH Clonal Rearrangement Assay with the Aid of a “Spike-in” Clonal SequenceInvivoscribe Marketing2021-02-11T23:36:10-08:00November 13th, 2019|Read more
Clonally-Related CD5+ CLL/SLL and CD10+ high grade B-cell lymphoma suggests common neoplastic progenitor with branched disease evolution, with therapeutic implicationsInvivoscribe Marketing2021-02-11T23:40:44-08:00October 15th, 2019|Read more
Stability and uniqueness of clonal immunoglobulin CDR3 sequences for MRD tracking in multiple myelomaInvivoscribe Marketing2021-02-11T23:43:09-08:00October 1st, 2019|Read more
Standardized Minimal Residual Disease Detection by Next-Generation Sequencing in Multiple MyelomaInvivoscribe Marketing2021-02-15T20:01:10-08:00June 6th, 2019|Read more
Establishment of Immunoglobulin Heavy (IGH) Chain Clonality Testing by Next-Generation Sequencing for Routine Characterization of B-Cell and Plasma Cell NeoplasmsInvivoscribe Marketing2021-02-11T23:46:14-08:00March 21st, 2019|Read more
German Supreme Court Upholds and Strengthens Invivoscribe FLT3 Patent Positionwmm2021-02-26T19:14:37-08:00March 28th, 2016|Read more
Novartis drug PKC412 (midostaurin) receives Breakthrough Therapy designation from the FDA for newly-diagnosed FLT3-mutated acute myeloid leukemia (AML)wmm2021-02-26T19:14:49-08:00February 18th, 2016|Read more
Invivoscribe Announces Long-Term Collaboration to Develop Immuno-Oncology Tests With Thermo Fisher Scientificwmm2021-02-26T19:15:19-08:00February 9th, 2016|Read more
Novartis drug PKC412 (midostaurin) improves overall survival by 23% in global Phase III study of AML patients with FLT3 mutationswmm2021-02-26T19:16:48-08:00December 5th, 2015|Read more