Autopsy report · NCT03075553
Nivolumab in Treating Patients With Relapsed or Refractory Peripheral T-cell Lymphoma
Cause of deathSlow enrollment
“due to poor response”
Life of this trial
- Registered 3 months before it started.
- Ran for about 2 years before it stopped.
- 12 participants enrolled.
- Results were posted on the registry 11 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 2
- Sponsor
- Mayo Clinic
- Sponsor type
- University, hospital or other
- Conditions
- Blastic Plasmacytoid Dendritic Cell Neoplasm; Hepatosplenic T-Cell Lymphoma; HTLV-1 Infection; NK-Cell Lymphoma, Unclassifiable; Primary Systemic Anaplastic Large Cell Lymphoma, ALK-Negative; Recurrent Adult T-Cell Leukemia/Lymphoma
- Interventions
- Laboratory Biomarker Analysis; Nivolumab
- Participants
- 12
- Sites
- 1
- Countries
- United States
Trials that died the same way
- A Clinical Investigation of the M2a- 38™ Hip System
“due to low follow up” - Myocet Plus Endoxan for Older Patients With Breast Cancer
“Due to poor accrual” - To Study and Compare the Clinical Course and Development of Organ Failure in Severe Acute Hepatitis Without Ascites, Non-cirrhotic and Cirrhotic Patients With Ascites [Acute on Chronic Liver Failure] and Acute Deterioration of Previously Decompensated Cirrhosis.
“Due to lack of funds” - Safety and Efficacy Study of AVB-S6-500 (Batiraxcept) in Patients With Advanced or Metastatic Clear Cell Renal Cell Carcinoma
“Due to 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.