Autopsy report · NCT01210443
Long-Term Open-Label, Safety Study Of Sitaxentan Sodium In Japanese Pulmonary Arterial Hypertension Patients
Cause of deathSafety
“Safety Issue: The trial was prematurely terminated on Dec 9, 2010, due to safety concerns, specifically new emerging evidence of hepatic injury.”
Life of this trial
- Registered 3 months before it started.
- Ran for about 1 month before it stopped.
- 2 participants enrolled.
- Results were posted on the registry 1 year after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 3
- Sponsor
- Pfizer
- Sponsor type
- Industry
- Conditions
- Hypertension, Pulmonary
- Interventions
- Sitaxentan
- Participants
- 2
- Sites
- 2
- Countries
- Japan
Trials that died the same way
- A Long-Term, Open-Label Study to Evaluate the Safety of Sitaxsentan Sodium Treatment in Patients With Pulmonary Arterial Hypertension
“This trial was prematurely terminated on Dec 9 2010 due to safety concerns, specifically emerging evidence of hepatic injury.” - Bactericidal Activity and Safety of Nicotinamide in Combination With Bedaquiline, Pretomanid, and Linezolid in Drug-susceptible Pulmonary Tuberculosis
“A temporary precautionary pause in enrolment into all arms of the trial was implemented on 21 July 2026, due to emerging hepatic safety signal. A protocol amendment is currently underway.” - Evaluation of Sentinel Lymph Nodes in Head and Neck Squamous Cell Carcinoma
“The trial was terminated early based on an interim review by the Data and Safety Monitoring Committee for positive efficacy outcome and no safety concerns.” - Impact of Molecular Testing on Improved Diagnosis, Treatment and Management of CAP
“The trial was stopped earlier than planned after an ad hoc interim analysis” - Merotocin in Mothers With Inadequate Milk Production and Infants Delivered Prematurely
“The trial was prematurely terminated. Termination was not because of safety concerns but due to slow recruitment.”
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.