Autopsy report · NCT04200352
A Study to Test if TEV-50717 is Safe and Effective in Relieving Abnormal Involuntary Movements in Cerebral Palsy
Cause of deathFutility
“Failure of TV50717-CNS-30080 (parent study) to meet the primary efficacy endpoint”
Life of this trial
- Registered 2 months before it started.
- Ran for about 3 years before it stopped.
- 44 participants enrolled.
- Results were posted on the registry 1 year 2 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 3
- Sponsor
- Teva Branded Pharmaceutical Products R&D, Inc.
- Sponsor type
- Industry
- Conditions
- Cerebral Palsy, Dyskinetic
- Interventions
- TEV-50717
- Participants
- 44
- Sites
- 30
- Countries
- Denmark, Israel, Italy, Poland, Russia, Spain, Ukraine, United Kingdom, United States
Trials that died the same way
- A Study With BPS-314d-MR-PAH-303 in Participants With Pulmonary Arterial Hypertension
“The pivotal study, BPS-314d-MR-PAH-302 (NCT01908699), failed to demonstrate efficacy.” - Safety of Rivipansel (GMI-1070) in the Treatment of One or More Vaso-Occlusive Crises in Hospitalized Subjects With Sickle Cell Disease
“The B5201003 OLE study was terminated based on the failure of the 'parent" B5201002 study to meet its efficacy endpoints. Termination was not due to safety.” - Study of Ruxolitinib (INCB018424) Administered Orally to Patients With Androgen Independent Metastatic Prostate Cancer
“According to the protocol, the sponsor terminated the study after it was determined that less than 2 of the first 22 patients showed a PSA50 response.” - A Study to Evaluate the Effects of GLPG2737 in Participants With Autosomal Dominant Polycystic Kidney Disease (ADPKD)
“The study was early terminated due to lack of efficacy.” - Oral EPI-7386 in Patients with Castration-Resistant Prostate Cancer
“Study was terminated early due to a lack of improved efficacy.”
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.