Autopsy report · NCT00973024
A Dose-ranging Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Low Back Pain
Cause of deathFutility
“Based on lack of efficacy in PAI2003, sponsor made the decision to discontinue the trial.”
Life of this trial
- Ran for about 1 year 8 months before it stopped.
- 389 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 2
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
- Sponsor type
- Industry
- Conditions
- Low Back Pain; Low Back Pain, Recurrent
- Interventions
- JNJ-42160443 3 mg; JNJ-42160443 1 mg; JNJ-42160443 6 mg/3mg; JNJ-42160443 10 mg; Matching Placebo
- Participants
- 389
- Sites
- 60
- Countries
- Belgium, Canada, Netherlands, United States
Trials that died the same way
- Safety and Efficacy of MAGE-A3/A6 T Cell Receptor Engineered T Cells (KITE-718) in HLA-DPB1*04:01 Positive Adults With Advanced Cancers
“The study was terminated due to the sponsor's decision to discontinue the clinical trial.” - A Dose Range Finding Study of JNJ-38518168 in Patients With Active Rheumatoid Arthritis in Spite of Treatment With Methotrexate
“The decision was made to prematurely discontinue this trial due to lack of efficacy.” - TAS-117 in Patients With Advanced Solid Tumors Harboring Germline PTEN Mutations
“The Sponsor had decided to terminate this clinical trial due to an insufficient rate of accrual of patients.” - Study of Avatrombopag for Temozolomide-induced Thrombocytopenia in Glioma (APATIT-G)
“PI and Sponsor decided to not proceed with the trial.” - A Phase 2a Pharmacodynamic Study of TAK-448 in Participants With Hypogonadotropic Hypogonadism
“Sponsor decision to terminate the study because the study did not achieve the primary efficacy objective.”
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.