Autopsy report · NCT05232864
Open-label Extension Study of Efficacy, Safety and Tolerability of Secukinumab in Patients With Active Lupus Nephritis
Cause of deathFunding or business, also futility
“Study terminated by sponsor based on a futility analysis of the core study CAIN457Q12301”
Life of this trial
- Registered 7 months before it started.
- Ran for about 1 year before it stopped.
- 31 participants enrolled.
- Results were posted on the registry 1 year after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 3
- Sponsor
- Novartis Pharmaceuticals
- Sponsor type
- Industry
- Conditions
- Lupus Nephritis
- Interventions
- Secukinumab
- Participants
- 31
- Sites
- 18
- Countries
- Australia, Brazil, Colombia, Czechia, Guatemala, Japan, Philippines, Portugal, Slovakia, South Korea, Spain, Thailand and more
Trials that died the same way
- A Study to Evaluate Long Term Safety and Efficacy of Recombinant Human Pentraxin-2 (rhPTX-2; PRM-151) in Participants With Idiopathic Pulmonary Fibrosis
“The study was terminated by Sponsor as the futility analysis outcome indicated that the study was unlikely to meet the predefined primary objective of the study. No new safety concerns were identified.” - Minocycline for the Treatment of Decreased Mental Function in HIV-Infected Adults
“This study was terminated early due to futility.” - A Dose Finding Study to Investigate the Safety and Effectiveness of GSK1070806 in Adult Participants With Moderate to Severe Atopic Dermatitis
“Sponsor decision to early terminate the study based on the pre-defined futility criterion for efficacy. No safety concerns were identified.” - Pembrolizumab (MK-3475) Versus Placebo Following Surgery and Radiation in Participants With Locally Advanced Cutaneous Squamous Cell Carcinoma (MK-3475-630/KEYNOTE-630)
“The study stopped due to futility” - Magrolimab + Azacitidine Versus Azacitidine + Placebo in Untreated Participants With Myelodysplastic Syndrome (MDS)
“Study discontinued due to futility based on a planned analysis”
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.