Autopsy report · NCT01712399
A Long Term Safety Study of Mavrilimumab in Adult Subjects With Rheumatoid Arthritis
Cause of deathRegulatory or ethics
“The study was terminated after approximately 3 years due to future clinical development plans, including ethical considerations.”
Life of this trial
- Registered 3 months before it started.
- Ran for about 2 years 11 months before it stopped.
- 409 participants enrolled.
- Results were posted on the registry 1 year 5 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 2
- Sponsor
- MedImmune LLC
- Sponsor type
- Industry
- Conditions
- Rheumatoid Arthritis
- Interventions
- Mavrilimumab 100 mg
- Participants
- 409
- Sites
- 52
- Countries
- Argentina, Bulgaria, Chile, Colombia, Czechia, Estonia, Germany, Greece, Hungary, Israel, Mexico, Poland and more
Trials that died the same way
- A Phase 1 Clinical Study of NXP800 in Subjects With Advanced Cancers and Expansion in Subjects With Ovarian Cancer
“Study terminated due to various reasons impacting the feasibility of future clinical development” - Surgical Intervention in Bariatric Patients: Excess Weight Loss in the Morbidly Obese Following Gastric Plication
“Study was terminated due to commercial considerations and potential patient attrition at 3 years. There were no patient safety or procedure efficacy reasons.” - Study To Determine The Pharmacokinetics Of Sulfasalazine In Children With Juvenile Idiopathic Arthritis
“Study terminated on 13 April 2016 for business reasons. No safety and/or efficacy concerns contributed to the termination of the study” - A Study of Tivozanib in Combination With Durvalumab in Subjects With Advanced Hepatocellular Carcinoma
“The study was terminated due to regulatory approval of newer therapeutic options and slower than anticipated accrual.” - A Long-Term Safety And Tolerability Study Of Bapineuzumab In Alzheimer Disease Patients
“The study was terminated on August 6, 2012, because 2 large Phase 3 studies showed no clinical benefit. This decision was not based on any new safety concerns.”
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.