Autopsy report · NCT01769443
Safety and Efficacy of Desensitization Therapy in Sensitized Participants Awaiting Heart Transplantation
Cause of deathSlow enrollment, also funding or business
“Inability to enroll within funding period”
Life of this trial
- Registered 5 months before it started.
- Ran for about 1 year 1 month before it stopped.
- 2 participants enrolled.
- Results were posted on the registry 1 year 4 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 2
- Sponsor
- National Institute of Allergy and Infectious Diseases (NIAID)
- Sponsor type
- US National Institutes of Health
- Conditions
- Primary Heart Transplant; Heart Transplantation; Heart Transplant
- Interventions
- bortezomib; plasmapheresis
- Participants
- 2
- Sites
- 14
- Countries
- United States
Trials that died the same way
- BREATHE-Easy Trial
“Funding completion date passed, inadequate enrollment” - Feasibility and Acceptability of a Remote Glucose Monitoring Program for Pregnant Marshallese Women
“Funding ended before enrollment” - Medical Therapies for Chronic Post-Traumatic Headaches
“inadequate enrollment, insufficient funds to continue enrollment” - Evaluate The Effectiveness Of Fospropofol (Lusedra®) For Induction Of Anesthesia
“Loss of funding before enrollment.” - Vitamine D Treatment in Chronic Heart Failure
“financial reasons / insufficient enrollment activity”
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.