Autopsy report · NCT04985968
The Efficacy and Safety of Cobitolimod in Participants With Moderate to Severe Active Left-Sided Ulcerative Colitis
Cause of deathFutility
“Due to futility”
Life of this trial
- Registered 4 months before it started.
- Ran for about 2 years 1 month before it stopped.
- 171 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 3
- Sponsor
- InDex Pharmaceuticals
- Sponsor type
- Industry
- Conditions
- Ulcerative Colitis
- Interventions
- Cobitolimod 250 mg; Cobitolimod 500 mg; Placebo
- Participants
- 171
- Sites
- 203
- Countries
- Australia, Austria, Belgium, Bosnia and Herzegovina, Brazil, Canada, Croatia, Denmark, France, Georgia, Germany, Hungary and more
Trials that died the same way
- Effects of Hypothermia Upon Outcomes After Acute Traumatic Brain Injury
“Futility” - Safety of FMT: OpenBiome Outcomes and Longitudinal Follow-up (STOOL) for Recurrent Clostridium Difficile Infection
“for futility” - Prevention of Unexplained Recurrent Abortion by Enoxaparine
“Stopped for futility” - The Effectiveness of Non-Pyrethroid Insecticide-Treated Durable Wall Liners as a Method for Malaria Control in Endemic Rural Tanzania
“futility ground” - Safety and Efficacy Study of AVB-S6-500 (Batiraxcept) in Patients With Advanced or Metastatic Clear Cell Renal Cell Carcinoma
“Due to business reasons”
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.