Autopsy report · NCT03590652
Daratumumab, Ixazomib, Pomalidomide, and Dexamethasone as Salvage Therapy in Relapsed/Refractory Multiple Myeloma
Cause of deathFutility
“The trial met its primary endpoint.”
Life of this trial
- Registered 4 months before it started.
- Ran for about 6 years 9 months before it stopped.
- 23 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 2
- Sponsor
- University of California, San Diego
- Sponsor type
- University, hospital or other
- Conditions
- Relapsed/Refractory Multiple Myeloma
- Interventions
- Ixazomib; Pomalidomide; Dexamethasone; Daratumumab-Hyaluronidase-Fihj@1,800 Mg-30,000 Unit/15 mL@SUBCUT@VIAL (ML)
- Participants
- 23
- Sites
- 4
- Countries
- United States
Trials that died the same way
- The Impact of IVIG Treatment on Critical Illness Polyneuropathy and/or Myopathy in Patients With MOF and SIRS/Sepsis
“The trial was terminated early due to futility in reaching the primary endpoint.” - Study to Determine the Efficacy of Uproleselan (GMI-1271) in Combination With Chemotherapy to Treat Relapsed/Refractory Acute Myeloid Leukemia
“Trial failed to meet primary endpoint.” - An Efficacy and Safety Study of Lanabecestat (LY3314814) in Early Alzheimer's Disease
“An independent assessment concluded the trial was not likely to meet the primary endpoint upon completion and therefore, trial stopped for futility” - Ibrutinib lead-in Followed by Venetoclax Plus Ibrutinib in Patients With RR CLL
“The board decision has been made to conclude the trial ahead of schedule. The primary endpoint has been successfully achieved and published, and funding was secured to support these three years of followup.” - Study to Assess LX201 for Prevention of Corneal Allograft Rejection or Graft Failure in Subjects Who Have Experienced One or More Rejection Episodes Following Penetrating Keratoplasty
“The primary efficacy endpoint was not met”
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.