Autopsy report · NCT00687674
Sorafenib, Lenalidomide, and Dexamethasone in Treating Patients With Relapsed or Refractory Multiple Myeloma
Cause of deathSlow enrollment, also safety
“Due to study design (and toxicity), this trial closed to accrual prior to opening the phase II portion.”
Life of this trial
- Registered 3 months before it started.
- Ran for about 3 years 3 months before it stopped.
- 13 participants enrolled.
- Results were posted on the registry 1 month after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1
- Sponsor
- Mayo Clinic
- Sponsor type
- University, hospital or other
- Conditions
- Multiple Myeloma and Plasma Cell Neoplasm
- Interventions
- dexamethasone; sorafenib tosylate; Lenalidomide
- Participants
- 13
- Sites
- 1
- Countries
- United States
Trials that died the same way
- A Phase 2b Study to Evaluate RIST4721 in Palmoplantar Pustulosis (PPP)
“Due to safety findings in ongoing Phase 2 trials.” - Dose Dense Therapy and Bevacizumab in Solid Tumors and Colorectal Cancer
“Trial did not move to Phase II portion due to poor tolerance of treatment” - Trial of High Dose Melphalan/Stem Cell Transplant With or Without Bortezomib
“Enrollment held for toxicity evaluation; then closed due to competing trial” - Chemotherapy, Radiation Therapy, and Cetuximab Followed by Surgery, Docetaxel, and Cetuximab in Treating Patients With Esophageal Cancer or Gastroesophageal Junction Cancer
“The study used a two-stage design. After stage one, the study was terminated due to excess toxicity.” - Venetoclax and Quizartinib in Treating Patients With FLT3-mutated Recurrent or Refractory Acute Myeloid Leukemia
“This study was terminated early due to other competing trials, therefore did not go on to the Phase II portion of the study.”
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.