Autopsy report · NCT03201159
A Pilot, Dose Escalating Study on VLX103 in Moderate Alcoholic Steatohepatitis
Cause of deathDrug or device supply
“Drug manufacturer ceased operations”
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- Withdrawn before it enrolled anyone.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- Withdrawn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 1
- Sponsor
- Gyongyi Szabo
- Sponsor type
- University, hospital or other
- Conditions
- Hepatic Steatosis
- Interventions
- VLX103
- Participants
- 0
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Oblimersen Sodium & Combination Chemotherapy in Treating Patients With Newly Diagnosed Diffuse Large B-Cell Lymphoma
“Manufacturer is no longer making the drug.” - Involved-field Radiotherapy-TNT Combined With PD-1 Inhibitor for pMMR Locally Advanced Rectal Cancer (Neo-Field I)
“Suspended due to lack of drug supply: the manufacturer ceased to provide investigational drug supply.” - The Study for Evaluate of Satety and Dfficacy of Hemostatic Device
“The company stopped manufacturing the product” - Bicalutamide and RO4929097 in Treating Patients With Previously Treated Prostate Cancer
“Drug was no longer available” - TGR-1202 (Umbralisib) in Treatment Naïve Patients With Chronic Lymphocytic Leukemia (CLL)
“Drug no longer available”
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.