Autopsy report · NCT00736450
Oblimersen Sodium & Combination Chemotherapy in Treating Patients With Newly Diagnosed Diffuse Large B-Cell Lymphoma
Cause of deathDrug or device supply
“Manufacturer is no longer making the drug.”
Life of this trial
- Ran for about 4 years 3 months before it stopped.
- 37 participants enrolled.
- Results were posted on the registry 5 years 11 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Early Phase 1
- Sponsor
- University of Nebraska
- Sponsor type
- University, hospital or other
- Conditions
- Contiguous Stage II Adult Diffuse Large Cell Lymphoma; Noncontiguous Stage II Adult Diffuse Large Cell Lymphoma; Stage I Adult Diffuse Large Cell Lymphoma; Stage III Adult Diffuse Large Cell Lymphoma; Stage IV Adult Diffuse Large Cell Lymphoma
- Interventions
- oblimersen sodium; rituximab; cyclophosphamide; doxorubicin hydrochloride; vincristine sulfate; prednisone
- Participants
- 37
- Sites
- 2
- Countries
- United States
Trials that died the same way
- A Pilot, Dose Escalating Study on VLX103 in Moderate Alcoholic Steatohepatitis
“Drug manufacturer ceased operations” - Active Surveillance Post-Approval Atudy of the Stelkast Surpass Acetabular System
“Product is no longer being manufactured and marketed.” - Phase I Study of CS-7017 and Bexarotene
“Drug no longer available” - Bicalutamide and RO4929097 in Treating Patients With Previously Treated Prostate Cancer
“Drug was no longer available” - CPI-613 (Devimistat) in Combination With Chemoradiation in Patients With Pancreatic Adenocarcinoma
“The pharmaceutical funder pulled funding and no longer plans to develop the drug further.”
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.