Autopsy report · NCT00602446
Deferasirox in Treating Patients With Iron Overload After Undergoing a Donor Stem Cell Transplant
Cause of deathSlow enrollment
“Due to slow accrual of patients”
Life of this trial
- Registered 5 months after it had already started.
- Ran for about 2 years 4 months before it stopped.
- 4 participants enrolled.
- Results were posted on the registry 3 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 2
- Sponsor
- Masonic Cancer Center, University of Minnesota
- Sponsor type
- University, hospital or other
- Conditions
- Breast Cancer; Iron Overload; Leukemia; Lymphoma; Multiple Myeloma and Plasma Cell Neoplasm; Myelodysplastic Syndromes
- Interventions
- deferasirox
- Participants
- 4
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Long-term Treatment for Cancer Patients With Deep Venous Thrombosis or Pulmonary Embolism
“Due to slow inclusion of patients” - Amifostine and Melphalan in Treating Patients With Primary Systemic Amyloidosis Who Are Undergoing Peripheral Stem Cell Transplantation
“Slow accrual and changes in clinical practice” - Efficacy and Safety Study of Cetuximab or Cetuximab Plus Docetaxel to Treat Prostate Cancer Before Prostatectomy
“lack of patient population - slow accrual” - Abiraterone-Rechallenge Study for CRPC Patients
“Lack of Patient accrual” - Trial of Two Central Venous Catheter (CVC) Flushing Schemes in Pediatric Hematology and Oncology Patients
“Poor patient accrual”
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.