Autopsy report · NCT02524639
Sirolimus for the Treatment of Hyperinsulinism
Cause of deathSlow enrollment
“Due to strict inclusion and exclusion criteria no subjects were enrolled”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Phase
- Phase 1, Phase 2
- Sponsor
- Children's Hospital of Philadelphia
- Sponsor type
- University, hospital or other
- Conditions
- Hyperinsulinism
- Interventions
- Sirolimus
- Participants
- 0
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Evaluation of Dextenza in Patients With Ocular GVHD and Effects on Ocular Surface Disease Outcomes
“Due to difficulty enrolling subjects whom had not meet the inclusion criteria” - Characterization of a Clinical Subpopulation in Children With Autism Spectrum Disorder
“No subjects enrolled” - Acetazolamide for the Prevention of Post Operative CSF Leak
“No participants were identified per inclusion/exclusion criteria” - Effects of Levothyroxine Treatment on Hemodynamic and Renal Functions in Subclinical Hypothyroidism
“No patient corresponding to inclusion criteria couldn't be enrolled in the study” - Evaluating a Novel Method of EEG Evoked Response Potential Analysis in Concussion Assessment, Young Adults and Adults
“No participant were enrolled”
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.