Autopsy report · NCT04478825
Efficacy and Safety of Rectally Administered BBT-401-1S in Subjects With Ulcerative Colitis
Cause of deathFunding or business
“Internal Company Decision”
Life of this trial
- Registered 11 months before it started.
- Ran for about 3 months before it stopped.
- 2 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1
- Sponsor
- Bridge Biotherapeutics, Inc.
- Sponsor type
- Industry
- Conditions
- Ulcerative Colitis
- Interventions
- BBT-401-1S
- Participants
- 2
- Sites
- 2
- Countries
- New Zealand
Trials that died the same way
- Clinical Performance Evaluation of the Hativ P30
“Company's internal decision.” - A Phase 1 Study of ADA-011 for Subjects With Advanced Solid Tumors
“Internal company decision (non-safety related)” - Influence of Variable Inflow Volume, Dwell Duration and Glucose Concentration on Ultrafiltration Volume in APD Patients
“Internal decision” - A Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of UCB8600 in Healthy Participants, Atopic Participants, and Chronic Spontaneous Urticaria Participants
“internal company decision; not safety related” - Impact of Omalizumab on Corticosteroid Use, Emergency Room Visits and Hospitalizations
“company decision”
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.