Autopsy report · NCT02780882
SOM230 Ectopic ACTH-producing Tumors
Cause of deathSlow enrollment
“Due to stringent inclusion/exclusion criteria, study investigator deemed it not feasible.”
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- Withdrawn before it enrolled anyone.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- Withdrawn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 2
- Sponsor
- Cedars-Sinai Medical Center
- Sponsor type
- University, hospital or other
- Conditions
- Ectopic ACTH Syndrome
- Interventions
- Pasireotide
- Participants
- 0
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Vaginal Estradiol Use in Pessary Care
“There is a lack of potential study participants at our study site that would meet inclusion criteria, therefore, the study is not feasible and is being terminated.” - Detailed Evaluation of Microchimerism
“Investigators could not identify subjects who met all inclusion criteria.” - High Versus Low Bicarbonate Bath in Critically-ill Patients Receiving Continuous Renal Replacement Therapy
“Due to the fact that we were unable to find subjects who met all inclusion and exclusion criteria it was determined to withdraw this study.” - Evaluation of a Physical Intervention for Persistent Post-Concussive Symptoms
“researchers did not find participants to meet the inclusion and exclusion criteria for the testing protocols” - Activity of Pre-Osteoclasts and Osteoclasts Over Time in Postmenopausal Women Treated With Denosumab or Zoledronic Acid
“The Investigator decided not to pursue this 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.