Autopsy report · NCT03654040
Liver Transplantation With Tregs at UCSF
Cause of deathFunding or business
“The study was terminated by the Sponsor prior to any participants receiving the investigational product.”
Life of this trial
- Registered 2 years 8 months before it started.
- Ran for about 1 year 10 months before it stopped.
- 42 participants enrolled.
- Results were posted on the registry 1 year 2 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1, Phase 2
- Sponsor
- National Institute of Allergy and Infectious Diseases (NIAID)
- Sponsor type
- US National Institutes of Health
- Conditions
- Liver Transplant
- Interventions
- arTreg; leukapheresis; cyclophosphamide; mesna; everolimus
- Participants
- 42
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Long-term, Non-interventional, Observational Study Following Treatment With Fate Therapeutics FT500 Cellular Immunotherapy
“This study was terminated by the Sponsor.” - Trial of Erlotinib in Patients With JAK-2 V617F Positive Polycythemia Vera
“The study was terminated by the sponsor” - A Study to Assess Recurrence of Actinic Keratosis in Participants Treated With Methyl Aminolevulinate Hydrochloride Cream or Vehicle Cream Who Achieved Complete Response to Treated Lesions in Earlier Study
“The study was terminated early as per Sponsor's decision” - Prospective Case-Series of Ligasure Advance Pistol Grip and LigaSure Blunt Tip
“The Sponsor terminated the study.” - Study to Investigate Comparative Efficacy, Safety and Immunogenicity Between AVT16 and Entyvio
“The study has been terminated based on Sponsor decision. This decision is not related to any safety concerns associated with the investigational products. It is related to the fact that study will be not required for product dossier submission.”
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.