Autopsy report · NCT02565147
Bivalirudin Infusion for Ventricular Infarction Limitation
Cause of deathFutility
“Futility at the interim analysis.”
Life of this trial
- Ran for about 1 year 6 months before it stopped.
- 78 participants enrolled.
- Results were posted on the registry 2 years 4 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 3
- Sponsor
- The Medicines Company
- Sponsor type
- Industry
- Conditions
- Acute Myocardial Infarction
- Interventions
- PPCI; Bivalirudin; Heparin
- Participants
- 78
- Sites
- 4
- Countries
- France, Netherlands
Trials that died the same way
- Sevoflurane and Percutaneous Coronary Intervention by Stent
“interim analysis suggests futility” - Efficacy and Safety Study of DP-b99 in Treating Acute Ischemic Stroke
“The result of a pre-planned interim futility analysis” - Study of M5049 in DM and PM Participants (NEPTUNIA)
“Based on interim analyses for futility” - Perioperative Treprostinil in Pediatric Patients Undergoing the Fontan Operation
“Interim futility analysis” - Interest of Intravitreal Injections of Anti-VEGF as Initial and Adjuvant Treatment in Coats Disease
“Study futility based on the interim analysis”
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.