Autopsy report · NCT03913130
Extension Study to Study PQ-110-001 (NCT03140969)
Cause of deathFunding or business
“Terminated \[Study prematurely terminated due to sponsor decision for reasons unrelated to safety\]”
Life of this trial
- Registered 3 months before it started.
- Ran for about 3 years 5 months before it stopped.
- 9 participants enrolled.
- Results were posted on the registry 3 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1, Phase 2
- Sponsor
- Laboratoires Thea
- Sponsor type
- Industry
- Conditions
- Leber Congenital Amaurosis 10; Blindness; Leber Congenital Amaurosis; Vision Disorders; Sensation Disorders; Neurologic Manifestations
- Interventions
- QR-110
- Participants
- 9
- Sites
- 3
- Countries
- Belgium, United States
Trials that died the same way
- Org 24448 (Ampakine) for Cognitive Deficits in Schizophrenia
“Study terminated at Sponsor's request.” - Satavaptan for the Prevention of Ascites Recurrence in Patients With Ascites Due to Cirrhosis of the Liver
“Study was terminated due to safety reason.” - Valproic Acid (VPA) for Acute Kidney Injury (AKI) in Liver Transplant Patients
“Study terminated by the Sponsor” - Pivotal Clinical Study of Endoscopic Ablation for Atrial Fibrillation (AF) in Patients That Have Failed Drugs
“Study terminated based on decision of Sponsor.” - Phase I Study of WX-037 Alone and in Combination With WX-554 in Solid Tumours
“Study terminated for business reasons”
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.