Autopsy report · NCT03593213
Clinical Trial Evaluating the Efficacy, Safety, and Tolerability of Cariprazine in a Dose-Reduction Paradigm in the Prevention of Relapse in Participants With Schizophrenia
Cause of deathRegulatory or ethics
“FDA Released Allergan from this post marketing requirement”
Life of this trial
- Ran for about 2 years 6 months before it stopped.
- 587 participants enrolled.
- Results were posted on the registry 1 year 1 month after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 3
- Sponsor
- AbbVie
- Sponsor type
- Industry
- Conditions
- Schizophrenia
- Interventions
- Cariprazine; Placebo
- Participants
- 587
- Sites
- 97
- Countries
- Bulgaria, Malaysia, Poland, Puerto Rico, Romania, Serbia, South Korea, Taiwan, Thailand, Ukraine, United States
Trials that died the same way
- Mitigate Immune-Mediated Loss of Therapeutic Response to Asfotase Alfa (STRENSIQ®) for Hypophosphatasia
“Sponsor decision following FDA release from the PMR.” - Continued Access Study of Adefovir Dipivoxil (ADV) for Patients w/Chronic HBV Infection.
“The study stopped due to marketing approval by the FDA.” - Study of the Safety and Effectiveness of Photochemically Induced Collagen Cross-Linking in Eyes With Keratoconus.
“No IND submitted to the FDA” - Electrical Impedence Tomography With ENLIGHT2100
“Device received FDA approval” - Perceval S Aortic Heart Valve Study- North America
“FDA approval”
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.