Autopsy report · NCT05609812
Atacicept in Subjects With Active Lupus Nephritis (COMPASS)
Cause of deathFunding or business
“Study recruitment is paused due to business reasons, but not due to regulatory or safety concerns.”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Phase
- Phase 3
- Sponsor
- Vera Therapeutics, Inc.
- Sponsor type
- Industry
- Conditions
- Lupus Nephritis (LN)
- Interventions
- Atacicept; Placebo
- Participants
- 0
- Sites
- 33
- Countries
- Puerto Rico, Spain, United States
Trials that died the same way
- Clinical Evaluation of Use of Prismocitrate 18 in Patients Undergoing Acute Continuous Renal Replacement Therapy (CRRT)
“Study halted due to low recruitment, unrelated to safety or efficacy reasons” - Biliary Interventions in Critically Ill Patients With Secondary Sclerosing Cholangitis (BISCIT)
“Study was stopped due to insufficient recruitment.” - Nasal High-frequency Jet Ventilation (nHFJV) Following Extubation in Preterm Infants
“Study stopped due to safety reasons.” - Focus on Fibre Study
“There were issues with recruitment so study was stopped” - Comparing Palliative Radiotherapy With or Without Carboplatin
“The study was stopped due to insufficient 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.