Autopsy report · NCT03506373
Ibrutinib and Ixazomib Citrate in Treating Newly Diagnosed, Relapsed or Refractory Waldenstrom Macroglobulinemia
Cause of deathFutility
“Discontinued after interim analysis for futility; no treatment successes observed in the first 12 patients”
Life of this trial
- Registered 4 months before it started.
- Ran for about 7 years 6 months before it stopped.
- 21 participants enrolled.
- Results were posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 2
- Sponsor
- Mayo Clinic
- Sponsor type
- University, hospital or other
- Conditions
- Recurrent Waldenstrom Macroglobulinemia; Refractory Waldenstrom Macroglobulinemia; Waldenstrom Macroglobulinemia
- Interventions
- Ibrutinib; Ixazomib Citrate; Laboratory Biomarker Analysis; Pharmacodynamic Study; Pharmacokinetic Study
- Participants
- 21
- Sites
- 2
- Countries
- United States
Trials that died the same way
- A Study of Idasanutlin With Cytarabine Versus Cytarabine Plus Placebo in Participants With Relapsed or Refractory Acute Myeloid Leukemia (AML)
“The study was stopped for futility based on efficacy results at the interim analysis; no unexpected safety findings were observed.” - Tissue Adhesive vs. Sterile Strips After Cesarean Delivery
“Based on results of an interim analysis, the study was halted for futility” - Effect of ITF2357 on Mucosal Healing in Patients With Moderate-to-severe Active Crohn's Disease
“As no safety warnings were detected, Interim analysis from the first 40 patients recommends to stop the trial for futility” - Removal Versus Retention of Cerclage in Preterm Premature Rupture of Membranes (PPROM)
“This trial was terminated following a futility analysis confirming futility of continuing the study” - Magrolimab + Azacitidine Versus Azacitidine + Placebo in Untreated Participants With Myelodysplastic Syndrome (MDS)
“Study discontinued due to futility based on a planned analysis”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.