Autopsy report · NCT03764774
A Study of LY3463251 in Healthy Participants
Cause of deathFutility
“Trial was terminated due to an insufficient benefit/tolerability ratio”
Life of this trial
- Ran for about 2 years before it stopped.
- 118 participants enrolled.
- Results were posted on the registry 4 years 11 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1
- Sponsor
- Eli Lilly and Company
- Sponsor type
- Industry
- Conditions
- Healthy
- Interventions
- LY3463251; Placebo
- Participants
- 118
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Endoscopic Full Thickness Resection of Gastric Subepithelial Tumors (FROST)
“According to study protocol the trial was terminated because the recruitment of trial participants was insufficient.” - A Study to Learn About the Effect of Avelumab First-Line Maintenance in Canadian People With Advanced Bladder Cancer
“The trial was terminated for strategic reasons. The decision was not based on any safety and/or efficacy concerns.” - A Study to Test the Effects of Nezavist at Different Doses in Healthy Adults
“The trial was terminated early due to regulatory constraints preventing the continuation of study conduct.” - TAS-117 in Patients With Advanced Solid Tumors Harboring Germline PTEN Mutations
“The Sponsor had decided to terminate this clinical trial due to an insufficient rate of accrual of patients.” - Study of Inlexisertib (DCC-3116) in Participants With RAS/MAPK Pathway Mutant Solid Tumors
“Trial terminated due to business decision, not based on any safety or efficacy concerns.”
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.