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Phase II Study of Ibrutinib in Patients With Symptomatic, Previously Untreated Waldenstrom's Macroglobulinemia, and Impact on Tumor Genomic Evolution Using Whole Genome Sequencing

Trial Profile

Phase II Study of Ibrutinib in Patients With Symptomatic, Previously Untreated Waldenstrom's Macroglobulinemia, and Impact on Tumor Genomic Evolution Using Whole Genome Sequencing

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 20 Feb 2025

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At a glance

  • Drugs Ibrutinib (Primary)
  • Indications Waldenstrom's macroglobulinaemia
  • Focus Therapeutic Use

Most Recent Events

  • 13 Dec 2022 Results identifying robust predictors for Ibrutinib response by multi omic genomics in MYD88 mutated Waldenstroms Macroglobulinemia, presented at the 64th American Society of Hematology Annual Meeting and Exposition
  • 05 Dec 2022 Status changed from active, no longer recruiting to completed.
  • 12 Sep 2022 Planned End Date changed from 1 Feb 2023 to 1 Oct 2022.

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