At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 31 enrolled
Drug / intervention
Ibrutinibdrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Phase II Study of Ibrutinib in Patients With Symptomatic, Previously Untreated Waldenstrom's Macroglobulinemia, and Impact on Tumor Genomic Evolution Using Whole Genome Sequencing
In Brief
A Phase 2 clinical trial evaluating Ibrutinib for Waldenstrom's Macroglobulinemia. Completed, enrolled 31 participants across 2 sites.
Detailed Summary
This research study is studying a drug called ibrutinib as a possible treatment for untreated Waldenstrom's Macroglobulinemia (WM).
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsWaldenstrom's Macroglobulinemia
CountriesUnited States
CollaboratorsPharmacyclics LLC.
Timeline
Phase 2CompletedFinished
20162017201820192020202120222023202420252026
First PostedNov 2015
Enrollment StartJan 2016
Primary CompletionNov 2022
TodayJul 2026
First PostedNov 13, 2015
Enrollment StartJan 1, 2016
Primary CompletionNov 1, 2022
TodayJul 2, 2026
Enrollment to primary: 6.8 yearsPosted 10.6 years ago
Interventions
Ibrutinibdrug